Pharmaceutical composition comprising bee venom-phospholipase A2 (BV-PLA2) for treating or preventing diseases related to degradation of abnormal regulatory T cell activity

Abstract

The present invention relates to a pharmaceutical composition for treating or preventing a disease related to abnormal suppression of regulatory T cell activity comprising a polypeptide comprising a bee venom-PLA2 amino acid sequence exclusive of a leader sequence as an active ingredient. The secretory bee venom-phospholipase A2 of the present invention activates a regulatory T cell and suppress a differentiation of Th1/Th7. Therefore, the present polypeptide can be used as a pharmaceutical composition for treating or preventing a disease related to abnormal suppression of regulatory T cell activity, i.e. autoimmune diseases, allergic diseases, or neurodegenerative diseases.

Claims

1. A method for treating rheumatoid arthritis, multiple sclerosis or psoriasis comprising: administering an effective amount of a composition comprising an isolated polypeptide to a subject having rheumatoid arthritis, multiple sclerosis or psoriasis, wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:6.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a schematic diagram briefly illustrating an experiment protocol for an allergic asthma animal model including the onset time when the experimental mice were sensitized with OVA and the time when they were treated with BV-PLA2 (secretory type).

(2) FIG. 2A-E shows graphs illustrating the effect of bee venom (BV) on the expression of Foxp3 of CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg and CD4.sup.+CD25.sup.+ Treg. (A) and (B) show the cytometry analysis results of the splenocytes of Foxp3.sup.EGFP C57BL/6 mice after treating them with various concentrations of bee venom (0, 0.001, 0.01, 0.1, 1, and 10 g/ml) for 24 hours followed by staining with CD4 and anti-CD25 antibodies. (A) shows the analysis results of CD25 and Foxp3 positive cells after gating on CD4.sup.+ T cells, and (A) shows the analysis results of expression rate of Foxp3.sup.EGFP after gating on CD4.sup.+CD25.sup.+ T cells. (C) through (E) show the results of flow cytometry analysis of murine cells isolated from a Foxp3.sup.EGFP C57BL/6 mouse after treating them with bee venom (1 g/ml) for 24 hours followed by staining with anti-CD4 and anti-CD25 antibodies. (C) shows the result of flow cytometry analysis of CD4.sup.+ T cells, (D) shows that of the CD4.sup.+CD25.sup. T cells, and (E) shows that of the CD4.sup.+CD25.sup.+ Treg cells. The numbers within the dot plots of (A), (C), and (D) respectively represent the percentage of cells belonging to the corresponding quadrant. The percentages of (B) and (E) represent a proportion of the gated Foxp3.sup.high cells in the CD4.sup.+CD25.sup.+ Treg. Experiments were repeated 3 times and one representative graph is shown, wherein data is shown via meanstandard error of the mean (SEM) (*p<0.05, ***p<0.001 vs. a PBS-treated cell group).

(3) FIG. 3A-D shows graphs illustrating the effect of bee venom (BV) on the proportion of various in vivo cell populations. Foxp3.sup.EGP C57BL/6 mice or C57BL/6 mice were administered with bee venom (0.01, 0.1, 1, and 10 mg/kg body weight) or an equal volume of brine daily for 5 days via intraperitoneal injection. The single-cell suspension of splenocytes was stained with fluorescence-labeled CD4, CD8a, CD19 and CD25 antibodies. (A) shows graphs illustrating the percentages of CD4.sup.+CD25.sup.+ Treg measured in murine splenocytes. (B) shows graphs illustrating the expression rates of Foxp measured after gating on the CD4.sup.+CD25.sup.+ Treg. The percentage is a proportion of Foxp3.sup.high cells being gated on the CD4.sup.+CD25.sup.+ Treg. (C) shows the expression rates of CD25 and/or Foxp3 measured after gating on the CD4.sup.+ T cells. The numbers within the dot plots of (A) and (C) respectively represent the percentage of cells belonging to the corresponding quadrant. (D) represents the percentage of the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg in the CD4.sup.+ T cells, or the percentage of the CD4.sup.+ T cells in the splenocytes, CD8.sup.+ T cells, and B cells. The data is indicated via meanSEM ((ns; not significant), *p<0.05, **p<0.01, ***p<0.001 vs. a brine-treated group).

(4) FIG. 4 shows a graph illustrating the in vitro inhibitory effect of bee venom against antigen-specific growth. The splenocytes of an experimental autoimmune encephalomyelitis (EAE)-induced C57BL/6 mice were stimulated with MOG.sub.35-55 peptide and counted 72 hours thereafter. The data is indicated via meanSEM ((ns; not significant), #p<0.001 vs. non-stimulated cells, ***p<0.001 vs. PBS-treated cells).

(5) FIG. 5A-D shows graphs illustrating the effects of bee venom on alleviating EAE via inhibition of Th1/Th17 differentiation. The C57BL/6 mice were immunized with MOG.sub.35-55 peptide. (A) shows a graph illustrating mean clinical disease scores measured by monitoring the mouse for 35 days after treating the mouse with bee venom (1 mg/kg body weight) from day 0 to 9th day after immunization (n=5/group). In (B) through (D), the mice were treated with bee venom (1 mg/kg body weight) from the 14th day to the 23.sup.rd day after immunization (n=12/group). (B) shows a graph illustrating mean clinical disease scores measured by monitoring the mouse for 35 days (n=12/group), (C) shows Th1/Th17 percentages measured after re-stimulating the splenocytes with PMA (50 ng/ml) and ionomycin (1 g/ml) for 5 hours in the presence of monensin (n=11/group), and (D) shows cytokine concentration in the serum measured after collecting on the 24.sup.th day (n=8/group). shows Th1/Th17 percentages measured after re-stimulating the splenocytes with PMA (50 ng/ml) and ionomycin (1 g/ml) for 5 hours in the presence of monensin (n=11/group), and (D) shows cytokine concentration in the serum measured after collecting on the 24.sup.th day (n=8/group). The data is indicated via meanSEM (*p<0.05, **p<0.01 vs. brine-treated group).

(6) FIG. 6A-C shows the effect of bee venom on alleviating EAE blocked due to the CD4.sup.+CD25.sup.+ Treg cell depletion. C57BL/6 mice were immunized with MOG.sub.35-55 peptide. Anti-CD25 antibodies were administered on the 13.sup.th day and the 19.sup.th day (respectively, the early stage treated with bee venom and an intermediate stage) of Treg depletion via intraperitoneal injection (A) shows a graph illustrating mean clinical disease scores measured by monitoring for 24 days. (B) and (C) show the results of analysis after sacrificing the mice on the 24.sup.th day after immunization (B) shows Th1/Th17 percentages measured after re-stimulating the splenocytes with PMA (50 ng/ml) and ionomycin (1 g/ml) for 5 hours in the presence of monensin (n=8/group), and (C) shows cytokine concentration in the serum measured after collecting on the 24.sup.th day (n=5/group). The data is indicated via meanSEM (ns; not significant).

(7) FIG. 7A-C shows the effect of bee venom on the increase of CD4.sup.+Foxp3.sup.+ Treg and the decrease of Th1/Th17. Foxp3.sup.+ Treg or Th1/Th17 was analyzed by gating on human CD4.sup.+ T cells. (A) shows the proportional ratio of CD4.sup.+Foxp3.sup.+ cells, which were treated with bee venom (1 g/ml) for 24 hours after separating PBMC and gating, indicated in percentages. (B-C) was treated with bee venom (1 g/ml) and anti-CD3/28 antibodies for 24 hours after separating PBMC. Then, the cells were re-stimulated with PMA (50 ng/ml) and ionomycin (1 g/ml) for 5 hours in the presence of monensin, and the result is shown in terms of population distribution. The numbers within the dot plots represent the percentage of cells belonging to the corresponding quadrant.

(8) FIG. 8A-B shows the comparative results of various bee venom components on immune-regulation inducing effect. The splenocytes of the Foxp3.sup.EGFP C57BL/6 mice were treated with bee venom or its component(s) for 24 hours, stained with anti-CD4 and anti-CD25 antibodies, and then analyzed via flow cytometry (A). The CD4.sup.+ T cells were gated, and CD25 and Foxp3 positive cells were analyzed. The numbers within the dot plots represent the percentage of cells belonging to the corresponding quadrant (B). The data is indicated via meanSEM (*p<0.05, **p<0.01 vs. a PBS-treated group).

(9) FIG. 9A-B shows the results of immune-regulation induced by human secretory BV-PLA2 (bee venom-phospholipase A2; secretory bee venom-PLA2). Human PBMC was re-stimulated with anti-CD3/28 antibodies and bee venom or BV-PLA2 for 24 hours. Then, the cells were re-stimulated with PMA (50 ng/ml) and ionomycin (1 g/ml) for 5 hours in the presence of monensin. the CD4.sup.+ T cells were gated, and Th1/Th17 was analyzed (A). The numbers within the to dot plots represent the percentage of cells belonging to the corresponding quadrant (B).

(10) FIG. 10A-B shows in vitro CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg population of splenocytes. The splenocytes stimulated with anti-mouse CD3 antibodies and anti-mouse CD28 antibodies were treated with various concentrations of BV-PLA2 (secretory type) for 3 days. The measured values were standardized with regard to the values of the stimulated control group. (A) shows CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg from control group and that from the splenocytes treated with BV-PLA2 (0.1, 1 g/ml). The numbers within the dot plots represent the percentage of cells belonging to the corresponding quadrant (B) shows the percentages of CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg, which was significantly increased in the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg-treated group compared to the control group. The data is indicated via meanSEM (standard error of the mean), and the analysis of the statistics was performed via Newman-Keuls multiple comparison test following the one-way ANOVA (*p<0.05, **p<0.01, ***p<0.001).

(11) FIG. 11 shows graphs illustrating the effect of BV-PLA2 (secretory type) on cytokine production. The splenocytes stimulated with anti-mouse CD3 antibodies and anti-mouse CD28 antibodies were treated with various concentrations of BV-PLA2 for 3 days. The supernatant of the resulting culture was recovered, centrifuged at 4 C. at 300 rcf for 10 minutes, and the resultant was stored at 70 C. for future use. The measured values were standardized with regard to the values of the stimulated control group. Cytokines were measured via flow cytometry using cytometric bead array (CBA). The data is indicated via meanSEM, and the analysis of the statistics was performed via Newman-Keuls multiple comparison test following the one-way ANOVA (*p<0.05, **p<0.01, ***p<0.001).

(12) FIG. 12 shows CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg populations in an ovalbumin (OVA)-induced asthma group, which are the results in, in a clockwise direction from the left upper end, control group (CON); a group with no treatment after OVA induction (OVA); a group introduced to with BV-PLA2 after OVA induction (OVA+PLA2); a group introduced with BV-PLA2 (secretory type) after OVA induction and anti-CD25 antibodies injection (OVA-T+PLA2); and a group with OVA induction and introduction with anti-CD25 antibodies injection (OVA-T). Specifically, isolated alveolar cells were stained with anti-CD4 allophycocyanine and anti-CD25 phycoerythrin (PE), and analyzed via flow cytometry. The data is indicated via meanSEM, and the analysis of the statistics was performed via Newman-Keuls multiple comparison test following the one-way ANOVA (n=4).

(13) FIG. 13 shows graphs illustrating the effect of BV-PLA2 (secretory type) on the production of IL-4 and IL-13 cytokines in bronchoalveolar lavage fluid (BALF). The level of Th2 inflammatory cytokine was shown higher in groups of OVA, OVA-T and (OVA-T+PLA2) than in groups of (OVA+PLA2) and CON. The data is indicated via meanSEM, and the analysis of the statistics was performed via Newman-Keuls multiple comparison test following the one-way ANOVA (***p<0.001, **p<0.05 vs. CON, n=4).

(14) FIG. 14 shows a graph illustrating the IgE level in the blood sera of the control group and the experimental groups. Blood samples were collected via cardiac puncture and the level of IgE in the samples was analyzed via ELISA. The data is indicated via meanSEM, and the analysis of the statistics was performed via Newman-Keuls multiple comparison test following the one-way ANOVA (*p<0.05, **p<0.01 vs. CON, n=4).

(15) FIG. 15 shows graphs illustrating the effect of BV-PLA2 (secretory type) on the recruitment of leucocytes in the airway of OVA-induced asthma mice. After establishing the OVA-induced asthma mouse model, BLAF was collected from the lungs of the mice. The total cells, eosinophils, macrophages, neutrophils, and lymphocytes were counted from the BALF. The data is indicated via meanSEM, and the analysis of the statistics was performed via Newman-Keuls multiple comparison test following the one-way ANOVA (*p<0.05, **p<0.01, ***p<0.001 vs. CON and OVA, n=4).

(16) FIG. 16A-E shows pictures illustrating the effect of BV-PLA2 (secretory type) on the recruitment of inflammatory cells into the lung tissues of OVA-induced allergic asthma mice. Balb/c Foxp3.sup.+EGFP Balb/c mice were sensitized with OVA and test-infected. The lung tissues were stained with hematoxylin and eosin (H&E) (400 magnification). The results shown represent: (A) a group of PBS-test infected mice treated with PBS (CON); (B) a group of OVA-test infected mice treated with PBS (OVA); (C) OVA-test infected mice treated with BV-PLA2 (0.2 mg/kg) (OVA+PLA2); (D) a group of OVA and anti-CD25 antibodies-test infected mice treated with BV-PLA2 (0.2 mg/kg) (OVA-T+PLA2); and (E) a group of OVA and anti-CD25 antibodies-test infected mice (OVA-T).

(17) FIG. 17A-E shows pictures illustrating the effect of BV-PLA2 (secretory type) on the histopathological changes in the lung tissues of OVA-induced allergic asthma mice. The lung tissues were stained with periodic acid-Schiff (PAS) (400 magnification). The results shown represent: (A) a group of PBS-test infected mice treated with PBS (CON); (B) a group of OVA-test infected mice treated with PBS (OVA); (C) OVA-test infected mice treated with BV-PLA2 (0.2 mg/kg) (OVA+PLA2); (D) a group of OVA and anti-CD25 antibodies-test infected mice treated with BV-PLA2 (0.2 mg/kg) (OVA-T+PLA2); and (E) a group of OVA and anti-CD25 antibodies-test infected mice (OVA-T).

(18) FIG. 18 shows a graph illustrating the effect of BV-PLA2 (secretory type) on the hyperresponsiveness in an OVA-induced asthmatic mouse model. The OVA-induced asthmatic mice had high P.sub.enh value at 50 and 100 mg/ml concentrations of methacholine (*p<0.01 vs. CON). The group (OVA+PLA2) show a significant decrease in the P.sub.enh value at 100 mg/ml concentration of methacholine used in the OVA-induced mice (regarding OVA, **p<0.01 vs. PLA2).

(19) FIG. 19A-E shows a graph illustrating the preventive effect of BV-PLA2 (secretory type) on dopaminergic (DA) neuronal cell death in substantia nigra (SN) of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-addicted mice. The MPTP-addicted mice were treated with BVPLA2 (0.5 mg/kg) or brine for 6 days starting 12 hours after the final MPTP injection. Some of the mice were administered with the anti-CD25 antibodies (1 mg/kg) one day prior to the MPTP injection. Seven days after the MPTP-addiction, the brain slices were immunostained with -TH antibodies for the DA neurons. (A) shows the result where the brine-injected mice were treated with brine, (B) shows the result where the MPTP-addicted mice were treated with brine, and (C) shows the result where the MPTP-addicted mice were treated with BV-PLA2. (D) and (E) show the number of TH positive neurons counted. For each experimental group, 8 to 9 experimental animals were used. In (A) through (C), the scale bar represents a length of 200 m (*p<0.001 vs. brine-treated control group, #p<0.01 vs. MPTP-addicted mice).

(20) FIG. 20A-B: (A) shows a vector structure for the expression of a recombinant BV-PLA2, and (B) shows the amino acid constitutions of four types of recombinant BV-PLA2.

(21) FIG. 21A-B: (A) shows an SDS-PAGE for confirmation of the recombinant proteins produced, and (B) shows the result of activity analysis for each enzyme.

(22) FIG. 22A through 22E show the results of flow cytometry analysis of the naturally occurring and recombinant BV-PLA2s stained with anti-CD4 and anti-CD25 antibodies for confirmation of their effects on the CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory T cells.

(23) FIG. 23 is a graph showing the effects of the naturally occurring and recombinant BV-PLA2s on Foxp3+ population among the CD4.sup.+ cells.

(24) FIG. 24A-B: (A) shows a result of SDS-PAGE for confirmation of the C-type recombinant BV-PLA2 and C-type mutant (H34Q) recombinant BV-PLA2, and (B) shows a comparison result of the activities of a natural secretory BV-PLA2 and the above enzymes.

(25) FIG. 25A-B shows (A) a graph showing the effects of the natural secretory BV-PLA2, C-type recombinant BV-PLA2, and C-type mutant (H34Q) recombinant BV-PLA2 on the Foxp3.sup.+ population among splenocytes, and (B) a graph showing the effects of the natural secretory BV-PLA2, C-type recombinant BV-PLA2, and C-type mutant (H34Q) recombinant BV-PLA2 on the Foxp3.sup.+ population among CD4.sup.+ cells.

BEST MODE

(26) In an aspect to accomplish the above objectives, the present invention provides a pharmaceutical composition, for treating or preventing diseases related to abnormal suppression of regulatory T cell (Treg) activity, containing a polypeptide including a BV-PLA2 amino acid sequence exclusive of a leader sequence as an active ingredient.

(27) As used herein, the term bee venom (BV) refers to a mixture of acidic and basic secretions generated in the abdomen of a honey bee (Apis mellifera) in the form of a colorless liquid, which includes as main components peptides such as melittin, apamin, and mast cell degranulating (MCD) peptide and phospholipase A2 (PLA2), etc., and a trace amount of various components. As used herein, the term bee venom-phospholipase A2 (BV-PLA2) refers to phospholipase A2 among the various complex mixtures of bee venom. As used herein, the term phospholipase A2 (PLA2) refers to an enzyme which serves the function of fatty acids via hydrolysis of glycerol at the 2.sup.nd carbon position. It specifically recognizes an sn-2 acyl bond of phospholipids and catalyzes hydrolytic activity thereby releasing arachidonic acid and lysophospholipids. Generally, PLA is not only found in bacteria, insects or serpent venoms but also in the tissues of mammals. The BV-PLA2 of the present invention may be derived from a honey bee (Apis mellifera) but is not limited thereto.

(28) BV-PLA2 may not be particularly limited as long as it has the PLA2 function derived from bee venom, and in particular, may be composed of a sequence represented by SEQ ID NO: 1. The SEQ ID NO: 1 is the total amino acid sequence that can be expressed from a gene regarding the publicly known BV-PLA2 (GenBank ID: ABQ28728.1), and is in the form of actual secretion. That is, it is the secretory type of BV-PLA2 in the form exclusive of a leader sequence at the N-terminus, and specifically, it may have an amino acid sequence represented by SEQ ID NO: 2 (consisting of 34th to 167 amino acids of SEQ ID NO: 1). As used herein, the term leader sequence refers to a sequence which is removed during the maturation process of from BV-PLA2 to a secretory bee venom-PLA2, and it may be a sequence corresponding to from the 1.sup.st to 33.sup.rd amino acids, and specifically, a sequence represented by SEQ ID NO: 3. In the present invention, the BV-PLA2 exclusive of the leader sequence is used as the same as the secretory BV-PLA2. The BV-PLA2 exclusive of the leader sequence is also called a matured type.

(29) In the present invention, the polypeptide including a BV-PLA2 amino acid sequence exclusive of a leader sequence may be one having an additional amino acid sequence on C-terminal region and/or N-terminal region of the BV-PLA2 amino acid sequence exclusive of a leader sequence. Specifically, the polypeptide may be one having an additional amino acid sequence represented by SEQ ID NO: 4 on the N-terminal region, or one having an additional amino acid sequence represented by SEQ ID NO: 5 on the C-terminal region. More specifically, the polypeptide may be one having an amino acid sequence represented by SEQ ID NO: 6. The above additional amino acid sequences may include a tag for purifying recombinant proteins.

(30) The polypeptide of the present invention including the bee venom-PLA2 amino acid sequence exclusive of a leader sequence, may be prepared by separating from bee venom by a known method, a recombinant expression, or may be used after purchasing those available in the market, or prepared by synthesis, but is not limited thereto.

(31) In an exemplary embodiment of the present invention, it was confirmed that a C-type recombinant BV-PLA2 (SEQ ID NO: 6; FIG. 20B), which was prepared by connecting additional amino acid residues for purification to both termini of the secretory type naturally-occurring BV-PLA2 amino acid sequence, exhibited an activity equivalent to or improved than that of the naturally-occurring BV-PLA2 (FIGS. 21B and 23). In contrast, an F-type recombinant BV-PLA2, which was prepared by including additional leader sequence to the N-terminus of the secretory type naturally-occurring BV-PLA2 amino acid sequence, or a B-type recombinant BV-PLA2, which was prepared by including additional leader sequence to the N-terminus and cutting off a part of the C-terminus (SEQ ID NOS: 7 and 8; FIG. 20B) failed to exhibit any significant enzyme activities (FIGS. 21B and 23).

(32) The BV-PLA2 of the present invention is a protein with a molecular weight of about from 10 kDa to 18 kDa, whose constitution is different from other PLA2s derived from other biological organisms or tissues, in particular, has only 9% of sequence homology to that of human PLA2 (based on the amino acid sequence of SEQ ID NO: 2).

(33) The BV PLA2 amino acid sequence not only includes a naturally-occurring amino acid sequence but also includes its sequence derivative (mutein) or its fragment exhibiting the BV-PLA2 activity. As used herein, the term amino acid sequence derivative refers to an amino acid sequence which differs from the naturally-occurring amino acid sequence by deletion, insertion, non-conservative substitution, or conservative substitution or a combination thereof by at least one amino acid residue in the naturally-occurring amino acid sequence.

(34) In an exemplary embodiment of the present invention, it was observed that the C-type mutant (H34Q) recombinant BV-PLA2, which was prepared by substituting histidine, the 34.sup.th amino acid from the N-terminus of the secretory naturally-occurring BV-PLA2, into glutamine, showed a drastic decrease in its activity (FIGS. 24 and 25). Accordingly, it is preferred that at least histidine, the 34.sup.th amino acid, be included as an essential component for enzyme activity.

(35) In the present invention, its fragment exhibiting the BV-PLA2 activity may have an amino acid sequence of SEQ ID NO: 9. A polypeptide including an amino acid sequence of a BV-PLA2 fragment exclusive of a leader sequence may be a polypeptide which further includes an additional amino acid sequence to the C-terminus or N-terminus of the amino acid sequence of BV-PLA2 fragment exclusive of a leader sequence. Specifically, it may be a polypeptide additionally including an amino acid sequence of SEQ ID NO: 4 to an N-terminus region, and a polypeptide additionally including an amino acid sequence of SEQ ID NO: 5 to a C-terminus region. More specifically, it may be a polypeptide including an amino acid sequence of SEQ ID NO: 10. The above additional amino acid sequence may include a tag for the purification of recombinant proteins.

(36) The substitution of amino acids in proteins or peptides without modifying the entire molecular activity is already known in the art (H. Neurath and R L. Hill, The Proteins, Academic Press, New York, 1979). The most conventional substitution is the substitution between amino acid residues of Ala/Ser, Val/Ile, Asp/Glu, Thr/Ser, Ala/Gly, Ala/Gly, Ala/Thr, Ser/Asn, Ala/Val, Ser/Gly, Thr/Phe, Ala/Pro, Lys/Arg, Asp/Asn, Leu/Ile, Leu/Val, Ala/Glu, and Asp/Gly. Depending on the situations, the substitution may be modified via phosphorylation, sulfation, acrylation, glycosylation, methylation, famesylation, acetylation, amidation, etc.

(37) The above described sequence derivatives may be those which exhibit the same biological activity to BV-PLA2 of the present invention or have an improved structural stability regarding heat, pH, etc.

(38) As used herein, the term regulatory T cell (Treg) refers to a kind of helper T cells (Th) also called suppressor T cells. Unlike other helper T cells exhibiting a humoral immune promoting effect by accelerating differentiation and activation of other leucocytes, Treg maintains immune tolerance by inhibiting immunity thereby enabling homeostasis. Treg can be divided into adaptive Treg, which includes Tr1 and Th3 cells produced during normal immune responses, and naturally-occurring Treg. The naturally-occurring Treg is generated in thymus, has positive to phenotypes for CD4, CD25 and Foxp3, and is distinguished from other T cells due to the presence of Foxp3, an intracellular molecule.

(39) As used herein, the term diseases related to abnormal suppression of Treg activity refers to a disease that occurs when the activity of regulatory T cells, which performs the functions of inhibition of autoimmunity, immune tolerance, inhibition of tissue damage by inflammation, etc., becomes abnormally deteriorated, and it includes allergic diseases, autoimmune diseases and neurodegenerative diseases, but is not limited thereto.

(40) The distinction between self and non-self antigens is the most important issue in the field of immunology, and due to the studies for the past few decades, various mechanisms involved in central tolerance and peripheral tolerance maintaining unresponsiveness to self antigens have been identified. In addition to the mechanisms of clonal deletion and anergy (functional inactivation), the suppression of the activity of self-reactive T cells has been also considered as an important mechanism in maintaining the tolerance for self-antigens.

(41) Among them, CD4.sup.+CD25.sup.+ T cells, known as naturally-occurring Tregs, have been confirmed to be important for the tolerance and prevention of autoimmune diseases by the experimental result that they can induce various kinds of autoimmune diseases in mice where CD25.sup.+ cell deficient T cells or CD25.sup. T cells were introduced via adoptive transfer (S. Sakaguchi, Annu. Rev. Immunol., 2004, 22: 531-562), before the discovery that foxp3 is an essential regulator gene important for Treg cell induction.

(42) It is known that foxp3 mutants can induce X-linked immunodeficiency syndrome (IPEX), which directly induces autoimmune diseases (type I diabetes, thyroiditis, etc.) from many organs in the endocrine system in humans (C. L. Bennett et al., Nat. Genet., 2001, 27: 20-21; R S. Wildin et al., Nat. Genet., 2001, 27: 18-20). This suggests the importance of CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory T cells in tolerance and for the prevention of autoimmune diseases.

(43) In addition to IPEX, the deficiency in Tregs or the loss of their suppressive function have been found to be associated with the pathogenic mechanism of autoimmune diseases such as type I diabetes, rheumatoid arthritis, multiple sclerosis, and psoriasis (M. Miyara et al., J. Immunol., 2005, 175: 8392-8400).

(44) Attempts have been made to use self antigen-specific Tregs for the treatment of autoimmune diseases and prevention of graft rejection. These attempts are mostly in the form of a somatic cell therapy, wherein the amplification of self antigen-specific Tregs is induced in vivo as in the case of peptide therapeutic vaccination using altered peptide ligand (APL) or administered after in vitro amplification, and are methods that inhibit the functions of effector T cells, which are specific to self antigens that induce autoimmunity (Y. Belkaid and B. T. Rouse, Nat. Immunol., 2005, 6: 353-360).

(45) Although pathogen-specific Tregs have a negative impact on the elimination of pathogens they serve an important role in the regulation of immunopathology by inhibiting tissue damage due to inflammation induced by pathogens, as in the prevention of autoimmune diseases (Y Belkaid and B. T. Rouse, Nat. Immunol., 2005, 6: 353-360).

(46) For example, in an experiment using mice infected with HSV through foodpads, deficiency in CD4.sup.+CD25.sup.+ T cells improved virus elimination by increasing CD8 but it aggravated T cell-mediated lesions (S. Suvas et al., J. Exp. Med., 2003, 198: 889-901).

(47) This has become an important issue to consider when conducting a therapeutic vaccination for the treatment of chronic virus infections including HIV and HCV by targeting Tregs such as removal of naturally-occurring T cells or blocking of effector molecules (Y Belkaid and B. T. Rouse, Nat. Immunol., 2005, 6: 353-360).

(48) As used herein, the term autoimmune diseases may include diseases that destroy self materials by wrongly determining self materials as foreign materials due to the inability to distinguish self materials from materials introduced from outside, which is the most important step in immune responses in the course of a series of actions for protecting self by destroying or inactivating materials introduced from outside. For example, they made include rheumatoid arthritis, systemic sclerosis, insulin-dependent juvenile diabetes by pancreatic islet cell antibody, alopecia areata, psoriasis, pemphigus, asthma, aphthous stomatitis, chronic thyroiditis, partial acquired aplastic anemia, primary liver cirrhosis, ulcerative colitis, Behcet's disease, Crohn's disease, silicosis, asbestosis, IgA nephropathy, poststreptococcal glomerulonephritis, Sjogren syndrome, Guillian Barre syndrome, dermatomyositis, polymyositis, multiple sclerosis, autoimmune hemolytic anemia, autoimmune encephalomyelitis, myasthenia gravis, Graves disease, polyarteritis nodosa, ankylosing spondylitis, fibromyalgia, temporal arteritis, Wilson's disease, Fanconi syndrome, multiple myeloma, and systemic lupus erythematosus, but is not limited thereto. The above autoimmune disease may be multiple sclerosis or autoimmune encephalomyelitis

(49) In an exemplary embodiment of the present invention, it was observed that bee venom inhibited the differentiation of Th1/Th17 thereby alleviating experimental autoimmune encephalomyelitis (EAE) (FIG. 5) while increasing the expression of Foxp3 in CD4.sup.+CD25.sup.+Foxp3.sup.+Treg and CD4.sup.+CD25.sup.+ Treg, which are regulatory T cells (FIG. 2) involved in immunities. Additionally, it was confirmed that Treg-deficiency can block the EAE alleviating effect of bee venom (FIG. 6), and thus suggested that Treg acts as an important mediator of EAE alleviation by bee venom. Accordingly, the increase of CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg and decrease of Th1/Th17 by bee venom in human CD4.sup.+ T cells were confirmed thereby verifying the immune regulation effect of bee venom in humans. Additionally, upon measurement of immune regulation inducing effects of various bee venom components, PLA2 (secretory type) was shown to have the highest immune regulation effect among the bee venom components (FIG. 8), and by its application in human cells, it was confirmed to enable induction of immune regulation in humans (FIG. 9).

(50) As used herein, the term allergic diseases refers to diseases, wherein substances which are non-toxic to normal people cause various symptoms in particular people due to abnormalities in their systems. The substances causing the allergic diseases are called allergens or antigens, and pollens, antibiotics, drugs, dusts, foods, cold air or sunlight, etc., may induce allergies. Examples of the allergic diseases include hives, sneezing, rhinorrhea, coughs, hay fever, ocular hyperemia, eczema, rashes, etc. The symptoms of the allergic diseases are hives, sneezing, pruritus, rhinorrhea, coughs, hay fever, ocular hyperemia, eczema, rashes, etc. The allergic diseases may include asthma, atopic dermatitis, conjunctivitis, rhinitis, and ulcerative colitis, but is not limited thereto. Preferably, the allergic disease is asthma, which accompanies symptoms such as airway constriction, increase in the secretion of mucus liquid in the lungs, dyspnea, and coughs.

(51) In an exemplary embodiment of the present invention, when an OVA-induced asthma mouse model, where the asthma was induced by sensitization with ovalbumin (OVA), was treated with BV-PLA2 there was a significant increase in CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg compared to the control group and other experimental groups (FIG. 12), thus confirming that BV-PLA2 has an excellent inhibitory effect against the introduction of inflammatory cells into lung tissues increased due to OVA sensitization (FIG. 16). Additionally, it also showed an effect of alleviating the airway hyperresponsiveness (AHR) (FIG. 18).

(52) As used herein, the term neurodegenerative diseases refers to diseases associated with symptoms such as degeneration, loss of functions, and often apoptosis of neurons. Since these symptoms are mostly progressive they are often highly destructive and patients with neurodegenerative diseases may experience extreme deterioration in their cognitive or motor performance. The neurodegenerative diseases may include, although not particularly limited thereto, Parkinson's disease (PD), Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), Huntington's disease (HD), fronto-temporal dementia, cortico basal degeneration, and progressive to supranuclear palsy (PSP).

(53) In an exemplary embodiment of the present invention, it was confirmed that BV-PLA2 (secretory type) decreases dopaminergic (DA) neuronal death in substantia nigra (SN) of a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-addicted mouse, i.e., an animal model with Parkinson's disease (FIG. 19).

(54) As used herein, the term prevention refers to all kinds of activities of inhibiting diseases related to abnormal suppression of regulatory T cell activity or delaying their occurrence by administering a pharmaceutical composition of the present invention, and the term treatment refers to all kinds of activities of improving or advantageously modifying the symptoms of the diseases related to abnormal suppression of regulatory T cell activity by administering the pharmaceutical composition of the present invention.

(55) The pharmaceutical composition of the present invention may further include a pharmaceutically acceptable carrier. As used herein, the term pharmaceutically acceptable refers to a non-toxic property to cells or humans being exposed to the composition. The above carrier to be used may be any one known in the art such as a buffering agent, a preservative, a pain-relieving agent, a solubilizing agent, an isotonic agent, a stabilizing agent, a base, an excipient, a lubricant, etc., without any limitation. The carrier, excipient, and diluent that may be included in the pharmaceutical composition of the present invention are lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methyl cellulose, microcrystalline cellulose, polyvinylpyrrolidone, water, methyl hydroxybenzoate, propyl hydroxybenzoate, talc, magnesium stearate, and base oil. For the preparation of formulations, the conventionally used filler, extender, binder, humectants, disintegrating agent, surfactant, diluent or excipient may be used. Examples of the usable typical surfactant that mediates the transmembrane transport are those derived from steroids, cationic lipids such as N-[1-(2,3-dioleoyl)propyl-N,N,N-trimethylammonium chloride] (DOTMA), or cholesterol hemisuccinate.

(56) In another aspect of the present invention, there is provided a method for preventing or treating diseases related to abnormal suppression of regulatory T cell activity including administering the above pharmaceutical composition to a subject in need thereof.

(57) As used herein, the term subject refers to all kinds of animals including humans in which diseases related to abnormal suppression of regulatory T cell activity have occurred or may occur, and the diseases related to abnormal suppression of regulatory T cell activity can be effectively prevented or treated by administering the pharmaceutical composition of the present invention to the subject. The pharmaceutical composition of the present invention may be administered in combination with a conventional therapeutic agent for the diseases related to abnormal suppression of regulatory T cell activity.

(58) As used herein, the term administration refers to an introduction of a particular material to a subject by a suitable method, and the above composition may be administered via any conventional administration route as long as they can allow the composition to arrive at the target tissue. For example, intraperitoneal administration, intravenous administration, intramuscular administration, intradermal administration, oral administration, topical administration, intranasal administration, intranasal administration, intrapulmonary administration, and intrarectal administration, but is not limited thereto. Solid formulations for oral administration may include tablets, pills, powders, granules, capsules, etc., and these solid formulations are prepared by adding at least one excipient in addition to the composition, for example, starch, calcium carbonate, sucrose, or lactose, gelatin, etc. Additionally, a lubricant such as magnesium stearate, and talc may be used, in addition to a simple excipient. Examples of liquid formulations for oral administration may include suspensions, medicines for internal use, emulsifiers, syrups, etc., and in addition to the frequently used simple diluents such as water and liquid paraffin, various excipients, for example, humectants, sweeteners, fragrant, preservatives, etc., may be included. However, peptides can be easily digested if administered orally, and thus a composition for oral administration is preferred to be formulated in such a manner that the active drug component is coated or protected from decomposition in the stomach. Formulations for parenteral administration may include sterile aqueous solutions, nonaqueous solvents, suspensions, emulsifiers, lyophilized preparations, suppositories. Examples of the nonaqueous solvents and suspensions include propylene glycol, polyethylene glycol, a vegetable oil such as olive oil, an injectable ester such as ethyl oleate. Examples of a base for the suppositories include witepsol, macrogol, Tween 61, cacao butter, laurinum, glycerogelatin, etc. For the improvement of stability or absorptivity of peptides, carbohydrates such as glucose, sucrose, and dextran; antioxidants such as ascorbic acid and glutathione; chelating materials, low molecular weight proteins or other stabilizers may be used.

(59) Additionally, the pharmaceutical composition of the present invention may be administered by any device which enables an active ingredient to move to a target cell. Preferable administration routes and formulations include those for intravenous injection, subcutaneous injection, intradermal injection, intramuscular injection, intravenous infusion, etc. Injections may be prepared using an aqueous solvent such as saline, ringer solution, etc.; a non-aqueous solvent such as a vegetable oil, high grade fatty acid eser (e.g., oleic acid ethyl, etc.), alcohols (e.g., ethanol, benzyl alcohol, propylene glycol, glycerin, etc.), etc., and may include a pharmaceutically acceptable carrier such as a stabilizer for preventing deterioration (e.g., ascorbic acid, sodium bisulfite, sodium pyrosulfite, BHA, tocopherol, EDTA, etc.), an emulsifier, a buffer for pH adjustment, a preservative for preventing microbial growth (e.g., phenylmercuric nitrate, thimerosal, benzalkonium chloride, phenol, cresol, benzyl alcohol, etc.).

(60) Meanwhile, the pharmaceutical composition of the present invention is administered in a pharmaceutically effective amount. As used herein, the term pharmaceutically effective amount refers to an amount sufficient for the treatment of diseases at a reasonable benefit/risk ratio applicable to a medical treatment without causing any adverse effects, and the level of an effective dose may be easily determined by a skilled person in the art according to factors including sex, age, body weight, health status of a patient, type of disease(s), severity of illness, drug activities, drug sensitivity, route and duration of administration, release rate, treatment period, mixing of drugs or other drug(s) used in combination, and others well known in the medical field. In general, an active ingredient may be administered daily in the amount of about from 0.01 mg/kg/day to 1000 mg/kg/day. For oral administration, it may be appropriate to administer in the amount of from 50 to 500 mg/kg, and may be administered at least once daily.

MODE FOR INVENTION

(61) Hereinafter, the present invention will be described in more detail with reference to the following examples. However, the following examples are provided for illustrative purposes only, and the scope of the present invention should not be limited thereto in any manner.

Example 1: Preparation of Experimental Animals

(62) Seven to eight-week old female C57BL/6 mice with a body weight of from 18 g to 23 g were purchased from Charles River Korea (Sungnam, Korea). Foxp3.sup.EGFPC57BL/6 (C. Cg-Foxp3tm2Tch/J) mice were purchased from Jackson Laboratory (Bar Harbor, Me., USA) and seven to eight week old male C57BL/6J mice with a body weight of from 21 g to 22 g were purchased from Charles River Breeding Laboratory (Yokohama, Japan). All mice were stored under aseptic conditions provided with air conditioning and 12 hour light/dark cycles. Additionally, all mice were given ad libitum access to food and water during the experiment. This study was approved by Animal Experimentation Ethics Committee of Kyung Hee University (Korea).

(63) 1.1. Experimental Autoimmune Encephalomyelitis (EAE)-Induced Experimental Animal Model

(64) Murine MOG.sub.35-55 (M-E-V-G-W-Y-R-S-P-F-S-R-V-V-H-L-Y-R-N-G-K) (SEQ ID NO:24) peptides were purchased from Peptron Inc. (Daejeon, Korea). The peptides were purified via HPLC to ensure 95% or higher of purity. For EAE induction, 200 g of MOG.sub.35-55 peptides, which was dissolved in CFA (Sigma-Aldrich, St. Louis, Mo., USA) containing 100 g of Mycobacterium tuberculosis, were administered to the hind flanks of mice via subcutaneous injection, and further administered with 400 ng of pertussis toxin (Sigma-Aldrich, St. Louis, Mo., USA) via intraperitoneal injection on day 0 and day 2. The mice were examined daily to check the presence of clinical signs of any disease(s), and the results were scaled in the range of from 0 to 5 at 0.5 intervals; wherein 0 denotes no clinical sign, 1 denotes relaxed tails, 2 denotes weakened hind legs or abnormal gait, 3 denotes complete paralysis of hind legs, 4 denotes complete paralysis of hind legs accompanying weakened front legs or paralysis of front legs, and 5 denotes being in a moribund state or death.

(65) 1.2. Allergic Asthma Experimental Animal Model

(66) Six to eight-week old female Foxp3.sup.+EGFP Balb/c mice were prepared. The mice on day 0 were divided into a negative control group (PBS-treatment; CON) (n=4) and an OVA-induced asthma group. The OVA-induced asthma group was subdivided into four groups (OVA-test-infected mice with PBS treatment (OVA); OVA-test-infected mice with BV-PLA2 (0.2 mg/kg) treatment (OVA+PLA2); OVA and anti-CD25 antibody-test-infected mice with BV-PLA2 (0.2 mg/kg) treatment (OVA-T+PLA2); and OVA and anti-CD25 antibody-test-infected mice (OVA-T), n=4/group). Briefly, the mice were sensitized via intraperitoneal (ip) injection of 100 g of ovalbumin (OVA; Sigma-Aldrich, St. Louis, Mo., USA), which was precipitated with 20 mg aluminum hydroxide in 100 l of PBS on day 0 and day 14. The mice were test-infected by directly administering 1% OVA in 50 l of PBS through their nostrils using a micropipette through a total of 6 administrations from day 20 to day 30. The mice in the negative control group were sensitized with PBS alone and test-infected.

(67) Treg-deficient mice were intraperitoneally injected with 0.25 mg anti-CD25 antibodies via on days 1, 8 and 15. Anti-mouse CD25 rat IgG1 (anti-CD25; clone PC61) was internally manufactured from hybridomas obtained from American Type Culture Collection (Manassas, Va., USA). The efficacy of Treg-deficiency as confirmed via flow cytometry analysis using PE-anti-mouse CD25 and fluorescein isothiocyanate (FITC)-anti-mouse CD4. The mice in the PLA2-test infected group were intraperitoneally injected with PLA2 at a concentration of 0.2 mg/kg through a total of 6 injections from day 3 to day 17. On day 31, airway hyperresponsiveness (AHR) was analyzed via (non-invasive) lung function measurement (All Medicus, Seoul, Korea), and on day 32 mice were sacrificed and various tissues were collected therefrom for analyses (FIG. 1).

(68) 1.3. 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-Addicted Parkinson's Disease Experimental Animal Model

(69) Seven to eight-week old male C57BL/6 mice with a body weight of from 21 g to 22 g (Charles River Breeding Laboratory, Yokohama, Japan) were prepared. For the construction of an MPTP-addicted model, the mice were intraperitoneally injected with an MPTP-HCl (a free base brine at 20 mg/kg; Sigma-Aldrich, St. Louis, Mo., USA) four times at two hour intervals. Twelve hours after the final MPTP injection, the MPTP-addicted mice were intraperitoneally injected with BV-PLA2 (0.5 mg/kg) once daily for six days. Some of the mice used as a control group were injected with BV-PLA2 alone or a vehicle. For Treg deficiency purpose, some of the mice were intraperitoneally injected with anti-CD25 antibodies (1 mg/kg) or normal rat IgG (1 mg/kg) once one day prior to the administration of MPTP

Example 2: Separation of Human Peripheral Blood Mononuclear Cells (PBMC)

(70) Human PBMC was separated from a healthy donor's blood collected using a BD VACUTAINER CPT tube containing heparin sodium. Briefly, the blood was directly collected into the tube via venipuncture and centrifuged at 1600 g for 20 minutes. The cells located on the upper portion of the centrifuged gel were recovered using a pipette and washed twice with PBS. The present invention was approved by the Institutional Review Board (IRB) of Korean Medicine Center of Kyung Hee University (Korea).

Example 3: Separation of Murine T Cells

(71) CD4.sup.+, CD4.sup.+CD25.sup. T cells and CD4.sup.+CD25+ Treg were separated from the splenocytes obtained from female Foxp3.sup.EGFPC57BL/6 mice via magnetic bead separation (CD4.sup.+ T cell separation kit and CD4.sup.+CD25.sup.+ regulatory T cell kit; Miltenyi Biotec, GmbH, Bergisch Gladbach, Germany) according to the manufacturer's instructions. The purities of all the populations were determined via flow cytometry analysis, and they conventionally reached 90% or higher.

Example 4: Reagents and Administration Routes

(72) Bee venom (BV), melittin, secretory bee venom-derived phospholipase A2 (BV-PLA2), mast cell degranulating peptide (MCD) and apamin were prepared in PBS solutions for in vitro experiments. Each component was used according to the proportion of the venom, that is, 50% of melittin, 10% of BV-PLA2, 2% of apamin, and 1% of MCD. Bee venom and all components of bee venom were purchased from Sigma-Aldrich (St. Louis, Mo., USA). Bee venom stock solution was prepared by dissolving bee venom in 0.9% brine at a concentration of 1 mg/ml. The bee venom stock solution was used after dilution according to concentrations for dose-dependent in vivo experiments. Bee venom (0.01, 0.1, 1, and 10 mg/kg body weight) or an equal volume of brine was intraperitoneally injected into the mice daily.

Example 5: Growth Analysis

(73) In an EAE-induced mouse model, the murine splenocytes immunized with MOG.sub.35-55 peptides were separated when the symptoms of the disease reached its culminating point. Briefly, the splenocytes were cultured at a concentration of 210.sup.6/ml in RPM 1640, which was added with 10% FBS, 50 IU/ml of penicillin, 50 g/ml of streptomycin, 10 g/ml of MOG.sub.35-55 peptide and bee venom (0.01, 0.1, 1, and 10 g/ml), for 72 hours. In order to determine the inhibitory effect of BV against antigen-specific growth, the number of splenocytes was counted using a hemocytometer. All the experiments were repeated three times.

Example 6: Flow Cytometry Analysis

(74) All the cytometry analyses regarding the samples prepared according to the methods described below were performed using CellQuest Pro Software (BD Biosciences, San Jose, Calif., USA) after collecting data using FASC Calibur flow cytometer (BD Bioscience, San Jose, Calif., USA).

(75) 6.1. Cell Preparation for Cytometry Analysis in EAE-Induced Animal Model Experiments

(76) In order to define Treg, a suspension of separated single-cells obtained from Foxp3.sup.EGFPC57BL/6 mice and splenocytes, and a healthy donor's PBMC were labeled with anti-CD4 and anti-CD25 or anti-Foxp3 monoclonal antibodies (eBioscience, San Diego, Calif., USA) according to the standard staining method. For the detection of intracellular cytokine expressions in mice and human cells, intracellular staining was performed using a cytofix/cytoperm kit (BD Biosciences, San Jose, Calif., USA) according to the manufacturer's instructions. Briefly, the cells were restimulated with 50 ng/ml of PMA and 1 g/ml of ionomycin (both from Sigma-Aldrich, St. Louis, Mo., USA) for 5 hours in the presence of BD GOLGISTOP protein transport inhibitor. The cells were stained with BD mouse or human Th1/Th2/Th17 phenotyping cocktail according to the manufacturer's instructions. For the detection of cytokine production, the secreted cytokines were measured using cytometric bead array (CBA; BD Biosciences, San Jose, Calif., USA) according to the manufacturer's instructions. Twenty four days after immunization, sera were collected and stored at 20 C. before use for CBA analyses.

(77) 6.2. Cell Preparation for Cytometry Analysis in Allergic Asthma-Induced Animal Model Experiments

(78) After separating CD4.sup.+ cells from the spleen of Foxp3.sup.EGFP Balb/c mice, they were seeded into a round bottom 96-well plate coated with anti-CD3e (2.5 g/ml) for one day at a concentration of 410.sup.6 cells/ml in the amount of 200 l/well, costimulated with anti-CD28 (2 g/ml), added with BV-PLA2 at a concentration of 0.1, 1 g/ml, and cultured in an incubator (37 C., 5% CO.sub.2) for three days. The resulting liquid culture was stored for cytokine measurement. Then, the resultant was added with CD4 and CD25 antibodies (anti-CD4-APC and anti-CD25-PE mAbs), which are cell surface markers, and placed at 4 C. for 30 minutes. The resultant was centrifuged at 300g after suspending in 1 ml of Dulbecco's phosphate buffered saline (DPBS) (welGENE) and the supernatant was removed. The resultant was resuspended in 300 l of DPBS, and the amount of expression of CD4.sup.+CD25.sup.+ Treg and Foxp3 were measured.

(79) Additionally, for the analysis of cells in lung tissues, the lung was isolated and washed with PBS to remove blood. The lung tissues were cut into small pieces and lysed in a 1% RBC lysis buffer (BD Pharmingen). Upon lysis of RBC, the lung tissues were passed through a 25 m cell strainer. The cells were washed three times and resuspended in FCM buffer solution (PBS containing 2% FBS and 0.1% NaN.sub.3). The suspension of the single-cells obtained from FOXP3.sup.EGFP Balb/c mice and the lung cells were labeled with anti-CD4-APC and anti-CD25-PE monoclonal antibodies according to the standard staining method, and the percentage of the cells stained with a particular sample was analyzed via FACS Calibur using CellQuest Software (BD Biosciences).

Example 7: Measurement of Cytokines in the Supernatant of Liquid Culture

(80) In an allergic asthma-induced model, splenocytes stimulated with anti-mouse CD3 antibodies and anti-mouse CD28 antibodies were treated with various concentrations of BV-PLA2 for three days. The supernatant of the liquid culture was recovered and centrifuged at 4 C. at a rate of 300 rcf for 10 minutes, and stored at 70 C. for future use. The level of measured cytokines was standardized relative to the cytokine level of the stimulated control group. Cytokines were measured via murine cytometric bead array (CBA, BD Biosciences, San Jose, Calif., USA). Briefly, 50 l of a sample or standard sample at a concentration of a base (0-5000 pg/ml) was added into 50 l of a mixture of a capture antibody bead solution and a detection antibody phycoeiythrin (PE) sample. Then, the resulting mixture was incubated at room temperature for two hours without sunlight, and washed to remove the unbound detection antibody PE sample. The data were collected using a flow cytometer (FACS Calibur, BD Biosciences Corp., San Jose, Calif., USA) and analyzed by a computer (CBA Software 1.1; BD Biosciences Corp.).

Example 8: Bronchoalveolar Lavage (BAL)

(81) In an allergic asthma-induced model, BAL was collected by infusion and extraction of 1 ml of ice-cold PBS. The above procedure was repeated 3 times and the lavage was collected (average volume of 2.0 ml). The recovered BAL (70-80%) was centrifuged at 13000 rpm for 10 minutes. Cell precipitate was resuspended in 1 ml of PBS and attached to a glass slide via cytocnetrifugation. The total number of viable cells was measured using a hemocytometer according to trypan blue exclusion. The differential counts on eosinophils, neutrophils, lymphocytes, and macrophages were determined based on smear samples of bronchoalveolar lavage fluid (BALF) samples (510.sup.5 cells/200 l) from an individual mouse stained with Diff-Quick (Life Technologies, Auckland, New Zealand) after counting 500 cells. Then, BALF was centrifuged and the supernatant to was stored at 70 C. The result was expressed as the total cell number10.sup.4.

Example 9: Analysis of Th2 Cytokine in BALF Via Enzyme-Linked Immunosorbent Assay (ELISA)

(82) In an allergic asthma-induced model, the concentrations of Th2 cytokine IL-4 and IL-13 were measured using a quantitative sandwich ELISA kit (BD, San Diego, USA for IL-4 and R&D, Minneapolis, USA for IL-13). A 96-well microplate was incubated at 4 C. overnight in a coating buffer solution along with anti-mouse IL-4 and IL-13 monoclonal antibodies, washed with PBS containing 0.05% Tween 20 (Sigma, MO, USA), and blocked respectively with PBS containing 5% FBS at 4 C. for one hour and with PBS containing 1% BSA for one hour. Then, 100 l of BALF was added thereto and incubated at room temperature for two hours. Secondary peroxidase was labeled in an assay diluent with biotinylated anti-mouse IL-4 and IL-13 monoclonal antibodies for one hour. Finally, the plate was treated with TMB base solution (KPL, San Diego, USA) for 30 minutes, and then added with 50 n1 of TMB stop solution to each well to stop the reaction. The absorbance at 450 nm was measured via a microplate reader (SOFT max PRO, version 3.1 Software, CA, USA). Here, the detection limit for IL-4 and IL-13 ELISA was 500 ng/ml and 100 ng/ml, respectively.

Example 10: Measurement of Serum IgE Titer Via ELISA

(83) In an allergic asthma-induced model, the mice were anesthetized with ether 32 days after inducing the disease, and blood samples were collected from the retro-orbital plexus of the mice. Sera samples were obtained via centrifugation and stored at 20 C. until analysis. Regarding the sera, a 96-well immune microplate (Costar, NY, USA) was coated with anti-mouse IgE monoclonal antibodies. The sera were diluted with PBS (assay diluents) containing 5% FBS at 1:250 ratio. The IgE measurement (BD Pharmingen) was used for a standardized sandwich ELISA according to the manufacturer's protocol. The absorbance at 450 nm was measured via a microplate reader (SOFT max PRO, version 3.1 Software, CA, USA). Here, the detection limit for IgE ELISA was 100 ng/ml, respectively.

Example 11: Histological Examination

(84) In an allergic asthma-induced model, trachea and lung tissues were removed from the mice. First, they were fixed with 4% paraformaldehyde, sunk into paraffin after dehydration, cut into 6 t m slices, and stained with Hematoxylin & Eosin (H&E) and Periodic Acid Schiff (PAS) reagents.

Example 12: Measurement of Airway Hyperresponsiveness (AHR) on Methacholine

(85) In an allergic asthma-induced model, on the day immediately following the final test-infection by administration of 50 l of PBS containing 1% OVA, the experimental animals were put into a barometric plethysmographic chamber (All Medicus, Seoul, Korea) and analyzed. The baseline reading was performed for 3 minutes. The enhanced pause (P.sub.enh) was calculated according to the manufacturer's protocol [i.e., (expiratory time/relaxation time1)(peak expiator)/flow/peak inspiratory flow)]. P.sub.enh is dimensionless parameter that represents a function of the proportion of maximal expiratory to maximal inspiratory box pressure signals and a function of the timing of expiration. The results were expressed in percentage increase of P.sub.enh according to the test-infection of methacholine (0, 50 and 100 mg/ml).

Example 13: Immunohistochemistry

(86) In an MPTP-addicted Parkinson's disease animal model, a brine containing 0.5% sodium nitrate and heparin (10 U/ml) was transcardially perfused through the experimental and fixed with 4% paraformaldehyde dissolved in 0.1M phosphate buffer (PB). The brain was removed and fixed in buffered 4% paraformaldehyde overnight, and stored in 30% sucrose solution maintained at 4 C. until it became sunk. The brain was fractioned into coronal slices with a thickness of 30 using a sliding microtome and frozen. All the fractions in six separated series were collected and subjected to immunochemical staining. The primary antibodies include those responding to tyrosine hydroxylase; TH; 1:2000, Pel-freez, Brown Deer, Wis., USA). The stained cells were visualized and then analyzed under brightfield microscope (Nikon, Tokyo, Japan).

Example 14: Preparation of Recombinant BV-PLA2 and Analysis of its Activity

(87) In order to prepare polypeptides including a BV-PLA2 amino acid sequence via recombinant expression, E. coli DH5 and E. coli BL21 (DE3) were respectively used as the strains for the expression of gene manipulation and protein expression.

(88) 14.1. Culturing Bacteria and Purification of Recombinant Proteins

(89) For a large scale production of proteins, 5 ml of a fresh overnight liquid culture of a selected bacteria strain was diluted with 1 L of LB medium containing ampicillin as an antibiotic. The recombinant E. coli BL21 (DE3) cells containing an expression plasmid were cultured at 37 C. while stirring until the absorbance at 600 nm reached about 0.9. The expression of the recombinant PLA2 was induced in a logarithmic growth phase by adding 1 mM isopropyl--d-thiogalactoside (IPTG) to the liquid culture. The overnight culture was centrifuged at 4 C. at a rate of 3000 rpm for 20 minutes and recovered the cells. The cell pellet was suspended in a buffer solution A (50 mM sodium phosphate buffer, pH 8.0, and 0.1 mM PMSF and 5 mM -mercaptoethanol). After pulverizing the cells using an ultrasonicator, they were centrifuged at 4 C. at a rate of 12000 rpm for 10 minutes, and washed with a buffer solution B (50 mM sodium phosphate buffer, pH 8.0, 2% Triton X-100, 20 mM EDTA, and 0.5 M NaCl) to prepare an insoluble pellet. Then, the resultant was modified in a buffer solution C (a buffer solution A containing 8 M urea) for at least 12 hours. The insoluble cell debris combined with the modified recombinant PLA2 was removed by centrifugation at 4 C. at a rate of 12000 rpm for 20 minutes. The histidine-labeled recombinant to PLA2 protein was purified via immobilized-metal affinity chromatography using His GraviTrap affinity column (GE Healthcare, Piscataway, N.J., USA). The histidine-labeled recombinant PLA2 protein was dialyzed twice at 4 C. using 3 L of 5 mM acetic acid for 12 hours and lyophilized.

(90) 14.2. Refolding of Proteins

(91) The lyophilized protein was dissolved in 7 M guanidine-HCl, and then added with 0.3 M Na2SO3 (pH 8.3) and a 1/20 volume of Thannhauser reagent for the sulfonification of cysteine thiol. The resulting solution was dialyzed against 3 L of a mixed solution containing 2 M urea, 4 mM EDTA, 0.1 M NH4Cl, and 20 mM sodium boronate (pH 8.3) for four hours and then the dialyzed solution was replaced with a fresh solution. After an additional four hours of dialysis, 56 ml of an aqueous solution of 0.5 M cysteine, and 17.5 mL of 0.2 M of cystine solution dissolved in 1 M HCl solution were added to the dialyzed solution, and the pH was adjusted to 8.3 using 10 M NaOH. At the appropriate time point, the dialyzed solution was transferred into a beaker wrapped with aluminum foil. When the activity reached the maximum level (generally from 18 to 24 hours after addition of cysteine and cystin), the proteins solution was decanted from the agglutinated precipitate, and dialyzed at 4 C. with 3 L of SP buffer solution (50 mM Tris-HCl, pH 9.0) for 14 hours. The protein purity was confirmed via SDS-PAGE using 15% (w/v) polyacrylamide for stacking and separating gels.

(92) 14.3. Activity Analysis of Recombinant Proteins

(93) Enzyme activities were determined by an ENZCHECK phospholipase A2 analysis kit (Invitrogen) which uses DOPC as a substrate. According to the manufacturer's protocol, the enzyme activities of BV-PLA2 and recombinant PLA2 were analyzed using the ENZCHECK phospholipase A2 analysis kit.

Example 15: Construction of Expression Plasmid and Site-Directed Mutagenesis

(94) The nucleotide sequence of the BV-PLA2 gene used in the present invention was inserted in advance into a cloning site of SalI-EcoRI of pEcoli-Nterm 6HN vector. The construction of the mutants of the BV-PLA2 gene was performed using primer pairs shown below: F-type BV-PLA2 (forward): 5-AAT GTC GAC CAA GTC GTT CTC GGA T-3 (SEQ ID NO: 12); F-type BV-PLA2 (Reverse): 5-AAG GAATTC TTATCAATA CTT GCG-3 (SEQ ID NO: 13); A-type BV-PLA2 (Forward): 5-AAT GTC GAC ATAATATAT CCA GGA-3(SEQ ID NO: 14); A-type BV-PLA2 (Reverse): 5-AAG GAATTC TCA CAG TTT GTAACA CTT-3(SEQ ID NO: 15); B-type BV-PLA2 (Forward): 5-AAT GTC GAC CAA GTC GTT CTC GGA T-3(SEQ ID NO: 16); B-type BV-PLA2 (Reverse): 5-AAG GAATTC TCA CAG TTT GTAACA CTT-3(SEQ ID NO: 17); C-type BV-PLA2 (Forward): 5-AAT GTC GAC ATAATATAT CCA GGA-3(SEQ ID NO: 18); C-type BV-PLA2 (Reverse): 5-AAG GAA TTC TTA TCAATA CTT GCG-3(SEQ ID NO: 19). A single mutation was introduced into a template, which is a genetic mutant of BV-PLA2 (H34Q), within the pEcoli-Nterm 6HN vector using a QuickChange site-directed mutagenesis kit (Stratagene). The reaction was performed using the primer pairs shown below: PLA2-H34Q (Forward): 5-GCATGC TGT CGAACC CAA GAC ATG TGC CCG GAC G-3(SEQ ID NO: 20); PLA2-H34Q (Reverse): 5-CGT CCG GGC ACA TGT CTT GGG TTC GAC AGC ATG C-3(SEQ ID NO: 21). The substituted nucleotides were underlined. The validity of the nucleotide sequences of mutants were confirmed by DNA sequencing analysis.

Example 16: Measurement of CD4+CD25+Foxp3+ Regulatory T Cells (Tregs)

(95) Flow cytometry analyses were performed for the samples prepared by the methods described below, and the proportional ratio of CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory T cell (Treg) for each cell was measured accordingly.

(96) 16.1. Measurement of CD4+CD25+Foxp3+ Regulatory T Cells (Tregs) from Murine Splenocytes

(97) Spleens were obtained from six to eight-week old female C57BL/6.sup.Foxp3-EGFP mice. The spleens were pulverized using a glass slide in the RPMI 1640 medium, and the cells were washed with RPMI 1640 medium, and then washed with red blood cell lysis buffer solution (Pharmingen). A 48-well plate with a flat bottom was coated at 4 C. with anti-mouse CD3 antibodies (2.5 mg/ml) overnight. The splenocytes were seeded into the 48-well plate at a cell density of 410.sup.6 cells/ml, treated with anti-mouse CD28 antibodies (2 mg/ml), and then treated with PBS, PLA2 or recombinant PLA2 for three days and seven days. After the three day and seven day treatments with the recombinant PLA2, the single-cell suspension of the splenocytes were incubated with anti-CD4-APC and anti-CD25-PE monoclonal antibodies using the standard staining method, and the stained samples were analyzed via a flow cytometer (FACScan Calibur, BD Biosciences). The collection and analysis of data were carried out using a Cell Quest 3.0f software.

(98) 16.2. Measurement of CD4.sup.+CD25.sup.+Foxp3.sup.+ Regulatory T Cells (Tregs) from Murine CD4.sup.+ T Cells

(99) Murine CD4.sup.+ Tcells were separated from spleens via MACS CD4 (L3T4) MicroBeads (Miltenyi Biotec Inc., Auburn, Calif., USA). The prepared single-cell suspension type cells were combined with the CD4 (L3T4) MicroBeads and incubated at 4 C. for 15 minutes.

(100) After incubation, the cells were washed with MACS buffer and resuspended in a small volume. The cells were passed through an LS column mounted to VarioMACS magnetic separator. The resultant was washed three to four times and the recovered CD4.sup.+ cells were resuspended in a complete RPMI 1640 medium. The 48-well plate with a flat bottom was coated at 4 C. with anti-mouse CD3 antibodies (2.5 mg/ml) overnight. The CD4.sup.+ cells were seeded into the 48-well plate at a cell density of 110.sup.6 cells/ml, treated in the same manner as in Example 16.1, and subjected to flow cytometry analysis.

Example 17: Analysis of Statistical Data

(101) The statistical analysis of data was performed via Prism 5.01 Software (Graph Pad Software Inc., CA, USA). All the values were indicated via meanS. E. M. (standard error of the mean). The differences between the control group and the groups treated with samples were determined one-way ANOVA or student t test. In all experiments, p<0.05 was considered to be of statistical significance.

(102) Results of Experiments

Experimental Example 1: In Vitro Direct Increase of CD4+CD25+Foxp3+ Treg by Bee Venom

(103) The CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg population and the expression of Foxp3 in the CD4.sup.+CD25.sup.+ Treg in Example 6.1 were analyzed via in vitro immunofluorescence method. Splenocytes were treated in vitro with bee venom at various concentrations (0, 0.001, 0.01, 0.1, 1, and 10 g/ml) and the effects according to the concentration were observed (FIGS. 2A and 2B). The bee venom (1 g/ml) noticeably increased the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg (P<0.05) and also increased the expression of Foxp3 in CD4.sup.+CD25.sup.+ Treg (P<0.001). The bee venom added to the splenocytes can presumably affect the CD4.sup.+ T cells directly or through antigen presenting cells (APC). In order to determine whether bee venom directly acts on CD4.sup.+ T cells, the CD4.sup.+ T cells were separated and treated with bee venom (1 g/ml) (FIG. 2C). When the CD4.sup.+ T cells were cultured without APC there was an increase in the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg (P<0.001). Subsequently, it was examined whether bee venom converts the CD4.sup.+CD25.sup. T cells into the CD4.sup.+CD25.sup.+Foxp3.sup.+ Tregs. When the CD4.sup.+CD25.sup. T cells were added with bee venom there was no increase in the Treg (FIG. 2D), whereas there was a noticeable increase in the expression of Foxp3 in the CD4+CD25+ Treg, which was cultured alone after bee venom treatment (FIG. 2E, P<0.001). The above results confirmed that bee venom increases the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg via direct influence on the CD4.sup.+CD25.sup.+ Treg instead of Treg induction from the CD4.sup.+CD25.sup. T cells.

(104) Effect of Treg-Specific Increase of Bee Venom and its In Vivo Efficacy According to its Dose

(105) In order to determine the optimum dose of bee venom for in vivo experiments, the experimental mice were treated daily with various amounts of bee venom (0, 0.01, 0.1, 1 and 10 mg/kg body weight) for five days. Notwithstanding with the various amounts of bee venom, only the mice treated with 1 mg/kg of bee venom showed a significant increase of the level of CD4.sup.+CD25.sup.+ Treg compared to that of the brine-treated control group (FIG. 3A, P<0.001). The Foxp3 expression in the CD4.sup.+CD25.sup.+ Treg showed a noticeable increase as is the case with in vitro experiment (FIG. 3B, P<0.05). Then, the effects of bee venom (1 mg/kg) on other immune cells containing CD4.sup.+ T cells, CD8.sup.+ T cells and B cells were analyzed. While there was no significant increase in the CD4.sup.+ T cells, CD8.sup.+ T cells and B cells as compared to the brine-treated control group, the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg showed a significant increase (FIGS. 3C and 3D). The above results confirmed that the dose of bee venom is a crucial factor in its efficacy and that 1 mg/kg may be the optimum dose for immunological therapy.

Experimental Example 3: In Vitro Myelin-Specific Growth Inhibitory Effect of Bee Venom

(106) The experiment results explained above indicate that bee venom has the potential therapeutic effect to be used for the treatment of autoimmune diseases. In order to confirm the assumption, firstly, antigen-specific growth analysis was performed (FIG. 4). The splenocytes of C57BL/6 mice immunized with MOG.sub.35-55 were restimulated with MOG.sub.35-55 peptide and counted the cell number 72 hours thereafter. As a result, it was confirmed that the myelin-specific growth of the splenocytes were inhibited by bee venom in a concentration-dependent manner (P<0.001).

Experimental Example 4: Alleviation of EAE in C57BL/6 Mice by Bee Venom Via Inhibition of Th1/Th17 Differentiation

(107) The possibility of whether the effect of bee venom can be interpreted via in vivo to experiments was sequentially examined. As the first step, the C57BL/6 mice immunized with MOG.sub.35-55 were treated daily with bee venom (1 mg/kg) from day 0 or day 14 for ten days (FIGS. 5A and 5B). The result showed that bee venom lowered severity of diseases as compared to that of brine-treated mice. This result shows that bee venom has the effects of prevention and treatment in EAE, which is an established animal model for multiple sclerosis (MS). MS and EAE have been already reported to be mediated by Th1/Th17 reactions. Accordingly, the present inventors studied the effect of bee venom whether it can inhibit Th1/Th17 differentiation. To this end, they conducted tests on the CD4.sup.+ T cells of EAE-induced mice (FIG. 5C). Both Th1 (P<0.05) and Th17 (P<0.05) differentiations were significantly blocked by bee venom treatment.

(108) Additionally, in order to test whether the Th1/Th17 differentiation affects the cytokine production, the sera cytokines profiles of the bee venom-treated mice and the brine-treated mice were analyzed on day 24 (FIG. 5D). The result showed that the bee venom treatment significantly reduced the production of other inflammatory cytokines including IFN- (P<0.05), IL-17A (P<0.01), TNF (P<0.05) and IL-6 (P<0.05) in the sera. Interestingly, the level of IL-4, which is the main Th2 (IL-4 producing CD4.sup.+ T cells) cytokine, was also reduced. The above results confirmed that bee venom has the inhibitory effect against the Th1/Th17 differentiation.

Experimental Example 5: Relationship Between the Effect of Bee Venom on EAE Alleviation and CD4+CD25+ Treg

(109) Experimental Example 1 showed that bee venom increased CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg. Additionally, Experimental Example 4 suggested that bee venom alleviates EAE by the inhibition of the Th1/Th17 differentiation. The above results imply that the increase in the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg by bee venom may prevent the Th1/Th17 differentiation thereby improving EAE. To confirm the above hypothesis, Treg deficiency was applied with anti-CD25 to monoclonal antibodies concurrently with the bee venom treatment on EAE. The previous results showed that the anti-CD25 monoclonal antibody is suitable for the CD4.sup.+CD25.sup.+ Treg deficiency in mice, and since most CD4.sup.+CD25.sup.+ T cells in the present invention exhibit positive result on Foxp3 and thus can be determined by Treg. Additionally, the present inventors analyzed the progress of EAE and the Th1/Th17 differentiation including cytokine production (FIG. 6). The result revealed that there was no distinct difference in clinical scores, the Th1/Th17 differentiation or cytokine production. Conclusively, Treg deficiency blocks the effect of bee venom on EAE. According to an exemplary embodiment, the bee venom treatment in mice alleviated EAE via its direct effect on the CD4.sup.+CD25.sup.+ Treg.

Experimental Example 6: Effect of Bee Venom on Human Treg and Th1/Th17 Differentiation

(110) Additionally, the effect of bee venom in humans was examined. In order to determine whether the level of Treg increases, a fresh PBMC separated from a healthy donor was incubated along with bee venom (1 g/ml) or PBS for 24 hours (FIG. 7A). The result revealed that, while the level of CD4.sup.+Foxp3.sup.+ Treg was increased in three out of the four bee venom-treated subjects (51.1917.94% increase vs. PBS), the bee venom treatment in the remaining one subject caused a slight decrease in the level of CD4.sup.+Foxp3.sup.+ Treg (5.16% decrease vs. PBS). Additionally, for the detection of the Th1/Th17 differentiation, the PBMC was treated with bee venom (1 g/ml) and anti-CD3/28 antibodies (FIG. 7B). Interestingly, the above three subjects, which showed an increase in Treg, showed a decrease in Th1 (34.964.93% decrease vs. PBS) and Th17 (26.298.08% decrease vs. PBS) rates, but the subject, which showed a slight decrease in Treg, did not show a decrease in Th1 (9.71% increase vs. PBS) and Th17 (1.14% increase vs. PBS) rates. The above data confirmed that bee venom can strengthen the inhibitory effect of Treg in humans and also that the effect can be applied to each individual subject.

Experimental Example 7: BV-PLA2 as an Active Ingredient of Bee Venom on Immune-Regulation in Mice and Humans

(111) The bee venom of Apis mellifera contains various peptides and proteins including melittin, BV-PLA2, MCD, and apamin. Accordingly, the present inventors conducted an experiment to examine which component of the various bee venom components may exert an effect on Treg in mice. In particular, splenocytes, separated from the Foxp3.sup.EGFPC57BL/6 mice, were treated with bee venom or each of the components including melittin, BV-PLA2, apamin and MCD (FIG. 8). According to the results, bee venom (P<0.05) and BV-PLA2 (P<0.01) induced a noticeable increase in the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg, whereas other compounds failed to show the same. Accordingly, the present inventors confirmed that BV-PLA2 is an active ingredient of bee venom involved in immune-regulation. Additionally, they also examined the immune-inhibitory effect of BV-PLA2 in humans. To this end, freshly separated PBMC was treated with bee venom, BV-PLA2 or PBS and anti-CD3/28 antibodies (FIG. 9). Bee venom and BV-PLA2 showed similar results reducing the populations in Th1 (bee venom: 30.4510.39%, BV-PLA2: 23.936.71% decrease vs. PBS) and Th17 (bee venom: 66.044.06%, BV-PLA2: 61.805.25% decrease vs. PBS). Conclusively, the above results confirmed that BV-PLA2 has an immune-regulation effect both in mice and humans.

Experimental Example 8: In Vitro Effect of BV-PLA2 on Inflammatory Cytokines in CD4+CD25+Foxp3+ Treg and Splenocytes

(112) The group treated with BV-PLA2 showed a higher increase in CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg population than the brine-treated group. Additionally, the group treated with BV-PLA2 showed a noticeably higher increase in the percentage of CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg than the brine-treated group (FIG. 10). The levels of IL-2, the Th1 cytokine capable of activating B cell by Th2, were more significantly decreased in the culture supernatant of the group treated with BV-PLA2 than in the brine-treated group. The above decrease in IL-2 indicates that BV-PLA2 can inhibit the inflammation caused by B cell immune responses. The levels of IL-10, a kind of Treg cytokines, were substantially increased in the group treated with BV-PLA2 than in the brine-treated group. However, BV-PLA2 failed to show any effect of statistical significance (FIG. 11).

Experimental Example 9: Effect of BV-PLA2 on CD4+CD25+Foxp3+ Treg in OVA-Induced Asthma Group

(113) In alveolar cells separated from an OVA-induced asthma mouse model, the OVA group showed a higher decrease in the CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg population than the CON group. The (OVA+PLA2) group showed a higher increase in CD4.sup.+CD25.sup.+Foxp3.sup.+ Treg population than the OVA group. The above results confirmed that BV-PLA2 can improve reduced Treg in allergic asthma (FIG. 12).

Experimental Example 10: Effect of BV-PLA2 on Th2 Cytokines (IL-4 and IL-13) in BALF

(114) The cytokine levels in the BALF of the control group and each mouse model of the experimental groups were measured. According to the result, the OVA, OVA-T and (OVA-T+PLA2) groups showed a higher increase in the level of Th2 inflammatory cytokine than the (OVA+PLA2) group and the control group (FIG. 13). BV-PLA2 could reduce the production of the inflammatory cytokine increased due to OVA treatment, but in the Treg-deficient group, BV-PLA2 treatment failed to show the above inhibitory effect. Accordingly, it was confirmed that Treg is involved in the inhibition of inflammatory cytokine secretion by BV-PLA2.

Experimental Example 11: Effect of BV-PLA2 on IgE Titer in Sera

(115) The OVA group showed a noticeably higher increase in IgE concentration in the serum than the CON group. This indicates that the asthma induction in an animal model of the present invention conducted in Example 1.2 was successfully performed. The (OVA-T+PLA2) group showed a significantly higher decrease in the serum IgE concentration than in the OVA, OVA-T and (OVA-T+PLA2) groups. BV-PLA2 could inhibit the increase in serum IgE concentration in OVA-induced allergic asthma mice, but the effect of BV-PLA2 failed to show in the Treg-deficient group (FIG. 14). This suggests that the inhibitory effect of BV-PLA2 against the increase of serum IgE concentration may occur via Treg activation.

Experimental Example 12: Effect of BV-PLA2 on Total Cells and Inflammatory Cells in BAL

(116) The OVA group showed a significantly higher increase in the number of total cells, eosinophils, and lymphocytes than the CON group. This indicates that the asthma induction in an animal model of the present invention conducted in Example 1.2 was successfully performed. The (OVA+PLA2) group showed a significantly higher decrease in the number of total cells, eosinophils, and lymphocytes than in the OVA, OVA-T and (OVA-T+PLA2) groups. BV-PLA2 could inhibit the increase of inflammatory cells such as the total BAL cells, eosinophils, lymphocytes in OVA-induced allergic asthma mice, but the effect of BV-PLA2 failed to show in the Treg-deficient group (FIG. 15). This suggests that the inhibitory effect of BV-PLA2 against the increase of the total BAL cells, eosinophils, lymphocytes may occur via Treg activation.

Experimental Example 13: Effect of BV-PLA2 on the Change in Lung Shape in an OVA-Induced Asthma Model

(117) In order to analyze the effect of PLA2 on the histological characteristics of asthma, the lung tissues of OVA-induced allergic asthma mice were subjected to H&E and PAS staining. According to the result, the lung tissue slices obtained from the mice exposed to OVA showed an airway inflammation, and pulmonary infiltration with eosinophils around the bronchial was observed (FIG. 16). In contrast, the lung tissue slices obtained from the mice treated with BV-PLA2 showed a decrease in airway inflammation. The periodic Acid Schiff (PAS)-positive mucus-count goblet cells present around the bronchial airway were detected in the OVA, OVA-T and (OVA-T+PLA2) groups. Meanwhile, BV-PLA2 treatment significantly reduced PAS-positive goblet cells around the bronchial airway (FIG. 17). The discovery suggests that BV-PLA2 has the potential of reforming an effective airway.

Experimental Example 14: Effect of BV-PLA2 on Airway Hyperresponsiveness in an OVA-Induced Asthma Model

(118) In order to confirm the inhibitory effect of BV-PLA2 against airway hyperresponsiveness, P.sub.enh values were measured. At concentrations of 50 mg/ml and 100 mg/ml of methacholine, the OVA, OVA-T and (OVA-T+PLA2) groups showed a noticeably higher increase in P.sub.enh value than in the BV-PLA2 group. Meanwhile, the group treated with BV-PLA2 showed a decrease in the increased P.sub.enh value at 50 mg/ml and 100 mg/ml concentrations of methacholine relative to the CON group of the OVA-induced asthma mice (*P<0.05, **P<0.01; FIG. 18).

Experimental Example 15: Effect of BV-PLA2 on Protection of Dopaminergic (DA) Neurons in Substantia Nigra (SN) in a Parkinson's Disease Animal Model

(119) Seven days after MPTP-addiction, the brain slices of an MPTP-induced Parkinson's disease animal model prepared in Example 1.3 were acquired, and DA neurons were immunostained with anti-TH antibodies. The BV-PLA2 treatment noticeably increased the number of TH.sup.+ neurons in SN to 32% compared to that of the mice in the MPTP-addicted control group (P<0.01; FIG. 1).

(120) BV-PLA2 treatment induced the activation of microglia after the infiltration of CD4.sup.+ T cells in SN. According to a recent report, CD4.sup.+CD25.sup.+ Treg mediates the protection of neurons by inhibiting microglia reaction in an MPTP-induced PD model. In order to confirm whether Treg is involved in the neuron protection by BV-PLA2, MPTP-addicted mice were intraperitoneally injected with anti-CD25 antibodies (1 mg/kg) one day prior to MPTP to administration, and thereby reduced the number of Treg cells. The BV-PLA2 treatment on the mice with a reduced number of Treg cells failed to reduce the DA neuronal death unlike the MPTP-addicted mice.

Experimental Example 16: Gene Synthesis and Construction

(121) The BV-PLA2 used in the present invention accounts for about from 10% to 20% of bee venom components, and the recombinant BV-PLA2 was prepared by RNA extraction from the honey bee (Apis mellifera), followed by cDNA synthesis, and PCR amplification using BV-PLA2-specific primers. The amplified gene was replicated into SalI and EcoRI restriction sites in the pEcoli-Nterm 6HN vector. The recombinant plasmid was transformed into E. coli strain DH5 and the recombinant plasmid DNA was extracted therefrom, and confirmed whether it was the correct recombinant BV-PLA2 via sequencing analysis of the recombinant plasmid DNA. For a large-scale production of the recombinant BV-PLA2, the recombinant plasmid were introduced into E. coli strain BL21 via transformation. The four types (F, A, B, and C) of BV-PLA2 used in the experiments were replicated into the pEcoli-Nterm 6HN vector in the same manner as described above (FIG. 20).

Experimental Example 17: Purification of Recombinant BV-PLA2 and its Enzyme Activity

(122) The various types of the recombinant BV-PLA2 prepared in the present invention were extracted in the same manner as described above, and confirmed via SDS-PAGE using 15% (w/v) polyacrylamide. As a result, it was confirmed that native secretory type BV-PLA2 is a protein with a size of 134 AA, F-type recombinant BV-PLA2 with 201 AA, A-type recombinant BV-PLA2 with 133 AA, B-type recombinant BV-PLA2 with 166 AA, and C-type recombinant BV-PLA2 168 AA (FIG. 21A; A-type not shown).

(123) Enzyme activities were analyzed for the above three types of recombinant BV-PLA2s and the native BV-PLA2 using an ENZCHECK phospholipase A2 analysis kit (Invitrogen), which utilizes DOPC substrate, as described in Example 14.3. According to the measurement, the activity of the native BV-PLA2 was 8 U/MW, and that of the F-type recombinant BV-PLA2 was 2 U/MW, but the enzyme activity of the B-type recombinant BV-PLA2 was not measured. In contrast, the enzyme activity in the C-type recombinant BV-PLA2 measured was shown to be similar to that of the native BV-PLA2, which is a positive control group (FIG. 21B).

Experimental Example 18: Effect of Recombinant BV-PLA2 on CD4+CD25+Foxp3+ Regulatory T Cell (Treg)

(124) In order to examine whether the recombinant BV-PLA2 can control the CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory T cells (Treg) in splenocytes, spleens were obtained from six to eight-week old C57BL/6.sup.Foxp3-EGFP mice. The splenocytes were stimulated with anti-mouse CD3 antibodies and anti-mouse CD28 antibodies, and treated with the native BV-PLA2 and the respective recombinant BV-PLA2 at a concentration of 1 mg/ml for three days, stained with anti-CD4-APC and anti-CD25-PE monoclonal antibodies, and were measured using a flow cytometer. The native BV-PLA2 showed a two-fold or higher of increase than that of the control group (1.66%), whereas F and B types showed no effect compared to that of the control group. In contrast, the C-type recombinant BV-PLA2 was shown to have 3.96% thus confirming that it is effective on the increase of CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory Tcells in the splenocytes (FIGS. 22A through 22E).

(125) Additionally, in order to examine whether the recombinant BV-PLA2 controls the CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory T cells (Treg) in CD4.sup.+ T cells, spleens were obtained from six to eight-week old C57BL/6.sup.Foxp3-EGFP mice. Only the CD4.sup.+ T cells were separated from the splenocytes via MACS CD4 (L3T4) MicroBeads, stimulated with anti-mouse CD3 antibodies and anti-mouse CD28 antibodies, treated with the native BV-PLA2 and the respective recombinant BV-PLA2 at a concentration of 1 mg/ml for three days, stained with anti-CD4-APC and anti-CD25-PE monoclonal antibodies, and were measured using a flow cytometer. The native BV-PLA2 showed a two-fold or higher of increase than that of the control group (2%), whereas F and B types showed no effect compared to that of the control group. In contrast, the C-type recombinant BV-PLA2 was shown to have 4% thus confirming that it is effective on the increase of CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory Tcells in the splenocytes (FIG. 23).

Experimental Example 19: Preparation of C-Type Mutant (H34Q) Recombinant BV-PLA2 and its Enzyme Activity

(126) The enzyme active site of the C-type mutant (H34Q) recombinant BV-PLA2 (SEQ ID NO: 11), prepared by the method described in Example 15 of the present invention, was modified from histidine to glutamine, and the C-type mutant (H34Q) recombinant BV-PLA2 was extracted in the same manner as described above, and confirmed via SDS-PAGE using 15% (w/v) polyacrylamide. The protein size of the C-type recombinant BV-PLA2 and the C-type mutant (H34Q) recombinant BV-PLA2, i.e., 171 AA, was confirmed via SDS-PAGE (FIG. 24A).

(127) The enzyme activity of the C-type mutant (H34Q) recombinant BV-PLA2 prepared above was measured using ENZCHECK phospholipase A2 analysis kit (Invitrogen), which utilizes DOPC as a substrate. According to the measurement, the activity of the native BV-PLA2 was 8 U/MW, and the activity of the C-type mutant (H34Q) recombinant BV-PLA2 was shown similar to that of the native BV-PLA2. However, the measured activity of the C-type mutant (H34Q) recombinant BV-PLA2 was low (FIG. 24B).

Experimental Example 20: Effect of C-Type Mutant (H34Q) Recombinant BV-PLA2 on CD4+CD25+Foxp3+ Regulatory T Cells (Treg)

(128) In order to examine whether the C-type mutant (H34Q) recombinant BV-PLA2 prepared above can control the CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory T cells (Treg) in the splenocytes and the CD4.sup.+ T cells, spleens were obtained from six to eight-week old C57BL/6.sup.Foxp3-EGFP mice. The sample of the splenocytes and the sample obtained by separating only CD4.sup.+ T cells from the splenocytes via MACS CD4 (L3T4) MicroBeads, were respectively stimulated with anti-mouse CD3 antibodies and anti-mouse CD28 antibodies, treated with the native BV-PLA2 at a concentration of 1 mg/ml, and the C-type recombinant BV-PLA2 and the C-type mutant (H34Q) recombinant BV-PLA2 at a concentration of 2 mg/ml, respectively, for seven days, stained with anti-CD4-APC and anti-CD25-PE monoclonal antibodies, and were measured using a flow cytometer. In the splenocytes, the native BV-PLA2 showed an increase by 28%, and the C-type recombinant BV-PLA2 showed an increase by 45%, respectively, compared to that of the control group, whereas the C-type mutant (H34Q) recombinant BV-PLA2 showed no effect compared to that of the control group (FIG. 25A). Meanwhile, in the CD4.sup.+ T cells, the native BV-PLA2 showed an increase by 7%, the C-type recombinant BV-PLA2 showed an increase by 9%, respectively, compared to that of the control group, whereas the C-type mutant (H34Q) recombinant BV-PLA2 showed no effect on the increase of CD4.sup.+CD25.sup.+Foxp3.sup.+ regulatory T cells (Treg), compared to that of the control group (FIG. 25B).