Recombinant BCG expressing HIV-1 p24 using pMyong2 vector system and use thereof

Abstract

Provided is a recombinant BCG employing a pMyong2 vector system to express HIV-1 p24 and a use thereof as a HIV-1 vaccine. rBCG-pMyong2-p24, which is a pMyong2 vector system, was found to induce the upregulation of HIV-1 p24 gag expression in rBCG and infected antigen-presenting cells (APC) and to induce improved p24-specific immune responses in vaccinated mice, compared to rBCG-pAL-p24 in a pAL5000 derived vector system. rBCG-pMyong2-p24 was identified to exhibit a higher p24-specific Ab production level than rSmeg-pMyong2-p24 in the same pMyong2 vector system. Therefore, the recombinant BCG employing rBCG-pMyong2-p24 to express HIV-1 p24 according to the present invention is identified to elicit enhanced immune responses to HIV-1 infection in mouse model systems and thus can be expected to be used as a prime vaccine in the heterologous prime-boost vaccination strategy against HIV-1 infection.

Claims

1. A recombinant Mycobacterium bovis BCG strain expressing the human immunodeficiency virus type 1 (HIV-1) p24 capsid (CA) protein set forth in SEQ ID NO: 1, wherein the p24 protein is expressed by a pMyong2-p24 vector system.

2. The recombinant Mycobacterium bovis BCG strain of claim 1, wherein the p24 protein is encoded by a qaq-gene derived from human immunodeficiency virus type 1 represented by a base sequence of SEQ ID NO: 2.

3. The recombinant Mycobacterium bovis BCG strain of claim 1, wherein the Mycobacterium bovis BCG is a Tokyo 172 strain.

4. An HIV-1 vaccine composition comprising the recombinant Mycobacterium bovis BCG strain of claim 1 as an active ingredient.

5. A method of inducing an HIV-1-specific immune response, comprising administering a vaccine composition comprising a therapeutically effective amount of the recombinant Mycobacterium bovis BCG strain of claim 1 as an active ingredient to a subject in need thereof.

6. The method of claim 5, wherein the recombinant Mycobacterium bovis BCG strain is live.

7. The method of claim 5, wherein the vaccine is not further attenuated.

8. The method of claim 5, wherein the vaccine is used as a prime vaccine in a prime-boost vaccination method.

9. The method of claim 5, wherein the subject has an infection caused by HIV-1 or co-infection caused by HIV-1 and Mycobacterium tuberculosis, or the subject is a patient with AIDS or tuberculosis.

Description

DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a view confirming the purity of p24 protein using polyacrylamide gel electrophoresis (SDS-PAGE) and Coomassie brilliant blue staining. M, molecular weight standard (Elpis Bio, Daejeon, Korea). Lane 1, purified p24 protein (10 μg).

(2) FIG. 2A is a view illustrating the cleavage map of each p24 expression vector disclosed in the present specification. As mycobacterium-E. coli shuttle vectors expressing an HIV p24 antigen, pMV306-p24, pALp24 and pMyong2-p24 vectors express p24 under the regulation of an hsp65 promoter derived from Mycobacterium bovis BCG, respectively.

(3) FIG. 2B is a view illustrating a growth curve of a p24 rBCG strain in a 7H9 medium supplemented with ADC and 100 μg/ml of kanamycin. In the case of wild-type BCG cultures, kanamycin was excluded from the 7H9 medium. For the growth curve, a culture aliquot was taken at each time point and OD600 was measured.

(4) FIG. 2C is a view comparing and illustrating the CFU levels of the p24 rBCG strains in infections of mouse macrophage J774A.1 (left) and mouse bone marrow-derived dendritic cells (right). The data represents two independent experiments. (The results are shown as mean±variance. *P<0.05; **P<0.01; ***P<0.001 (Student's t-test).

(5) FIG. 3A is a view confirming p24 expression in the rBCG strains using ELISA.

(6) FIG. 3B is a view confirming the p24 expression of the rBCG strains using western blotting analysis. Proteins were extracted from wild-type BCG (Lane 1) and rBCG strains (Lane 2: rBCG-pMV306-p24, Lane 3: rBCG-pAL-p24, Lane 4: rBCG-p24). Purified p24 protein was used as a positive control (Lane 5). M, molecular weight standard (Elpis Bio, Daejeon, Korea). Individual membranes are separated by white spaces and marker lanes are separated by black vertical lines. The expression levels of p24 are illustrated in the present drawing, and the western blotting images were cropped from a full-length blot to improve clarity. Full-length blotting images are illustrated in the following FIG. 3C.

(7) FIG. 3C is a view illustrating full-length original blotting images of the cropped images of FIG. 2C. Western blotting was performed using the antibodies illustrated in the present drawing. The cropped parts are shown by a solid line.

(8) FIG. 3D is a view confirming the stability of p24 expression in the rBCG-pMyong2-p24 strain passaged on a 7H10 agar plate containing kanamycin using western blotting. Proteins were extracted from wild-type BCG (Lane 1) and rBCG-pMyong2-p24 strains at their respective passage points (Lane 2: 1st passage, Lane 3: after 4th passage, Lane 4: after 6th passage, Lane 5: after 8th passage, Lane 6: after 10th passage, Lane 7: after 12th passage). Purified p24 protein was used as a positive control (Lane 8). M, molecular weight standard (Elpis Bio, Daejeon, Korea). After a membrane was cut as an internal control from an upper size membrane, p24 was detected using Hsp65 antibody (Abcam). Individual membranes are separated by white spaces and marker lanes are separated by black vertical lines.

(9) FIG. 3E is a view illustrating full-length original blotting images of the cropped images of FIG. 2D. Western blotting was performed using the antibodies illustrated in the present drawing. The cropped parts are shown by a solid line.

(10) FIG. 3F is a view confirming the stability of p24 expression in the rBCG-pMyong2-p24 strain passaged on a 7H10 agar plate without kanamycin using western blotting. Proteins were extracted from wild-type BCG (Lane 1) and rBCG-pMyong2-p24 strains at their respective passage points (Lane 2: 1st passage, Lane 3: after 4th passage, Lane 4: after 5th passage, Lane 5: after 6th passage, Lane 6: after 7th passage, Lane 7: after 8th passage, Lane 8: after 9th passage, Lane 9: after 10th passage, Lane 10: after 11th passage, Lane 11: after 12th passage). Purified p24 protein was used as a positive control (Lane 12). M, molecular weight standard (Elpis Bio, Daejeon, Korea). After a membrane was cut as an internal control from an upper size membrane, p24 was detected using Hsp65 antibody (Abcam). Individual membranes are separated by white spaces and marker lanes are separated by black vertical lines.

(11) FIG. 3G is a view illustrating full-length original blotting images of the cropped images of FIG. 2F. Western blotting was performed using the antibodies illustrated in the present drawing. The cropped parts are shown by a solid line.

(12) FIG. 3H is a view measuring the expression levels of p24 after infection with wild-type BCG and rBCG strains (rBCG-pMV306-p24, -pAL-p24, and -pMyong2-p24), respectively in mouse microphage J774A.1 (left) and mouse bone marrow-derived dendritic cells (right). The data represents two independent experiments. (The results are shown as mean±variance. *P<0.05; **P<0.01; ***P<0.001 (Student's t-test).

(13) FIG. 3I is a view comparing the expression levels of p24 in BMDCs infected with different M.O.I (1 and 10 M.O.I; multiplicity of infection (M.O.I)) of rBCG-pAL-p24 and rBCG-pMyong2-p24 strains on days 1 and 3 using ELISA. The results are shown as mean±variance in duplicate wells. *P<0.05; **P<0.01; ***P<0.001 (Student's t-test).

(14) FIGS. 4A to 4D are views illustrating T cell proliferation levels induced by BMDCs infected with p24 rBCG strains. (FIG. 4A) a schematic view of the T cell proliferation analysis schedule. Two mice were injected with the p24 protein (30 μg/mouse), and 7 days later, the splenocytes of the mice were classified into CD4 and CD8T cells and labeled with CFSE. The day before co-culture, DCs were infected with each strain (10 M.O.I). After CFSE-labeled CD4/CD8 T cells and infected DCs were co-cultured for 4 days, the above cells were analyzed for T cell proliferation; (FIGS. 4B and 4C) Results of flow cytometric analysis of CFSE-labeled CD4 and CD8 T cell proliferation of BMDCs infected with p24 rBCG strains (FIG. 4D) ELISA measurement of IL-2 released in supernatants of CD4 (left panel) and CD8 (right panel) cells using MLR analysis. The data represents three independent experiments. The results are shown as mean±variance. *P<0.05; **P<0.01; ***P<0.001 (Student's t-test).

(15) FIGS. 5A to 5C are views illustrating in vivo immune responses induced by p24 rBCG strains, respectively: (FIG. 5A) a schematic view of immunization performed for in vivo immunological analysis. Each group (5 mice/group) was immunized twice with wild-type BCG, two rBCG strains and a rSmeg strain, respectively, at 4 week intervals. 4 weeks after the final immunization, mice were sacrificed and spleens and blood samples were collected for immunoassay; (FIG. 5B) splenocytes of the mice vaccinated with the p24rBCG strains were stimulated in vitro and then detected using IFN-γ secretion level ELISPOT assay. Representative images of ELISPOT membranes of each group are shown below the graph. (−), Negative control; (+), Positive control; (FIG. 5C) After in vitro stimulation of splenocytes of the mice vaccinated with p24 rBCG strains, IL-2, IFN-γ and IL-6 cytokine levels were detected using ELISA assay. A total of 5 mice per group were analyzed. The data represents two independent experiments. The results are shown as mean±variance. *P<0.05; **P<0.01; ***P<0.001 (Student's t-test).

(16) FIG. 6 is a view illustrating humoral immune responses induced by p24 rBCG strains. The p24-specific immunoglobulin subtypes (IgG2a, IgG1, and total IgG) were measured at 450 nm using ELISA, and the OD values for IgG2a and IgG1 subtypes and the ratios of IgG2a/IgG1 were compared. Serum samples of five mice per group were analyzed. The data represents two independent experiments. The results are shown as mean±variance. *P<0.05; **P<0.01; ***P<0.001 (Student's t-test).

(17) FIG. 7 is a view illustrating the cytotoxic T lymphocyte responses in mice immunized with the rBCG strains. The CTL response occurs when p24-stimulated splenocytes (effector cells) and p24 epitope peptides (A9I) are allowed to react with P815 cells (target cells) in vitro. A total of 3 mice per group were analyzed. The data represents two independent experiments. The results are shown as mean±variance. *P<0.05; **P<0.01; ***P<0.001 (Student's t-test).

(18) FIGS. 8A to 8C are views illustrating the results of comparison between p24-specific immune responses by injection of the p24 protein and different M.O.I of rBCG-pMyong2-p24 strains. (FIG. 8A) is a set of results of ELISPOT assay for comparing IFN-γ secretion levels after in vitro stimulation of splenocytes obtained from mice hypodermically injected with the p24 protein (30 μg/mouse) and different CFUs (1×10.sup.6 and 1×10.sup.7 CFU) of rBCG-pMyong2-p24 strains (1 week intervals, injected twice). Representative images of ELISPOT membranes of each group are shown below the graph. (−), Negative control; (+), Positive control. The results are shown as mean±variance in triplicate. **P<0.01; ***P<0.001 (Student's t-test); (FIG. 8B) is a set of results of detecting p24-specific immunoglobulin subtypes (IgG2a, IgG1, and total IgG) by ELISA. Serum samples of three mice per group were analyzed. The results are shown as mean±variance in triplicate. **P<0.01; ***P<0.001 (Student's t-test); (FIG. 8C) is a view illustrating cytotoxic T lymphocyte responses due to the response of splenocytes (stimulated with A9I, p24 epitope peptide; effector cells) obtained from p24 protein- and rBCG-pMyong2-p24 injected mice and A9I peptide-pulsed P815 cells (target cells). Serum samples of three mice per group were analyzed. The results are shown as mean±variance in triplicate. **P<0.01; ***P<0.001 (Student's t-test).

MODES OF THE INVENTION

(19) The present invention is based on the discovery that recombinant Mycobacterium bovis BCG strains expressing the HIV-1 p24 antigen may be effectively used in vaccines.

(20) Thus, in an aspect, the present invention relates to a recombinant Mycobacterium bovis BCG strain expressing a p24 protein of HIV-1, and the p24 protein is expressed by the pMyong2-p24 vector disclosed on FIG. 2A.

(21) The p24 capsid (CA) protein expressed by the vector according to the present invention is linked to the 3′-terminus of a matrix protein (MA) in an untreated Gag polyprotein. The p24 capsid (CA) protein includes two domains at the N- and C-termini, which play important roles in HIV budding and capsid structure. The p24 expressed by the vector according to the present invention is derived from HIV-1, the sequence thereof is included in GenBank No. KM390026.1d, or corresponds to an amino acid of SEQ ID NO: 1 or nt 3161 to 3856 of the sequence of SEQ ID NO: 4, and sequence variants thereof may also be used as long as they act as an antigen for the purpose according to the present application. The p24 expressed by a strain according to the present application may act as an antigen against HIV infection when administered to the human body.

(22) In the strain according to the present invention, p24 is expressed by the pMyong2 vector specifically disclosed on FIG. 2A. The recombinant BCG strain including pMyong2-p24 according to the present invention can induce higher levels of HIV-1p24 protein expression and deliver more p24 antigens to macrophages than other rBCG strains using a pAL5000 or pMV306 induction system, so that the recombinant BCG strain is shown to be very excellent.

(23) Furthermore, a BCG recombinant strain including the pMyong2-p24 is shown to be able to improve the T cell proliferation capacity of infected bone marrow-derived dendritic cells (BMDCs) and induce enhanced T cell effector functions and Th1-biased humoral immune responses in vaccinated mice. In addition, a rBCG-pMyong2-p24 strain according to the present application is attenuated due to a delayed initial growth, so that a stronger immune response can be maintained by presenting more antigens to phagocytic cells. These results indicate that rBCG-pMyong2-p24 according to the present invention may be an effective candidate vaccine for HIV-1 or co-infection with HIV-1 and tuberculosis.

(24) Thus, in another aspect, the present invention relates to an immunogenic, vaccine or immunotherapeutic composition for HIV infections including the strains disclosed in the present specification. HIV is a type of retrovirus which destroys the human immune system, and when infected with HIV, HIV progresses to AIDS because the host's immune system is weakened, and the risk of opportunistic infections by bacteria, viruses, fungi, parasites, and the like is remarkably increased. AIDS is acquired immune deficiency syndrome and refers to various symptoms which appear due to a reduction in the immune function of the human body as a result of HIV infection.

(25) The vaccine composition according to the present invention may induce a p24-specific immune response, for example, deliver more p24 antigens to phagocytic cells, improve T cell proliferation capacity, and induce enhanced T cell effector functions and Th1-biased humoral immune responses, so that it is possible to prevent HIV infection or reduce, alleviate, and/or treat symptoms due to the infection.

(26) A vaccine is generally administered twice or more typically in the form of a prime-booster. In this case, the same vaccine is administered several times (homologous), or different types of vaccines including the same antigen are administered (heterologous). In an exemplary embodiment, the vaccine according to the present application is used as a prime vaccine in a homologous or heterologous prime-boost. The rBCG-pMyong2-p24 strain according to the present application has a high expression level of the p24 antigen and a high antigen presenting capacity, so that the rBCG-pMyong2-p24 strain is advantageous for use in prime vaccines because the strain can induce a sufficient p24-specific immune response in naive individuals.

(27) The mycobacteria used in the composition according to the present invention are as described above, and in particular, live viable bacteria may be used. In particular, the rBCG-pMyong2-p24 strain according to the present invention is naturally attenuated due to a delayed initial growth, so that a stronger immune response can be maintained by presenting more antigens to phagocytic cells.

(28) As used herein the term “vaccine” is a biological preparation containing an antigenic material which immunizes the living body, and refers to an immune source which causes immunity in the living body by being infused or injected into an organism for the prevention or treatment of AIDS and/or tuberculosis

(29) As used herein, the “individual” refers to a subject in need of treatment of a disease, and more specifically, refers to a mammal such as a human or a non-human primate, a mouse, a rat, a dog, a cat, a horse, and a cow.

(30) As used herein, the “immune response” refers to a response to the introduction of an HIV-1 antigen, for example, a universal HIV-1 antigen through a provided DNA plasmid vaccine, and is used in the present application to mean the activation of the host's immune system, for example, the mammalian immune system. The immune response may be in the form of a cellular or humoral response, or both.

(31) The vaccine composition according to the present invention may be formulated for systemic or topical administration, and may include a pharmaceutically acceptable excipient, carrier and/or vehicle, for example, a phosphate buffered saline solution, distilled water, a water/oil emulsion, a wetting agent, an emulsifying agent, a pH adjusting agent, and the like, but is not limited thereto.

(32) The vaccine composition according to the present invention may include an immunoadjuvant, particularly any material or compound capable of promoting or increasing a T-cell mediated response, if necessary. In an exemplary embodiment, the immunoadjuvant may be used when bacteria which have been killed by chemicals or heat are included in the composition. The immunoadjuvant is known in the art, and it is possible to use, for example, aluminum hydroxide, aluminum phosphate, aluminum potassium sulfate, a crosslinked polyacrylic acid polymer, dimethyldioctadecylammonium bromide (DDA), an immunomodulator, lactoferin, an IFN-gamma derivative, and the like. In an exemplary embodiment, the crosslinked polyacrylic acid polymer includes a Carbopol c homopolymer or copolymer, the lymphokine includes IFNgamma, IL-1, IL-2, or IL-12, and the IFN-gamma derivative may include poly I:C, but is not limited thereto. In an exemplary embodiment, the aluminum hydroxide, aluminum phosphate, or aluminum potassium sulfate, which is a synthesized sugar polymer, is included in an amount of about 0.05 to 0.1 wt %, and the crosslinked polyacrylic acid polymer may be included in an amount of 0.25 wt %, but the amounts are not limited thereto.

(33) The composition according to the present invention may be administered topically or systemically, may be administered once or multiple times, and may be administered by various routes, such as subcutaneously, intradermally, intramuscularly, or intravenously, or may be administered via an oral, nasal or inhalation route. In an exemplary embodiment, the composition according to the present invention is administered once by intramuscular injection.

(34) The vaccine composition according to the present invention may be prepared as a liquid solution or suspension suitable for the route of administration, or may be formulated in a solid form, which is dissolved or suspended in a solution prior to injection.

(35) As used herein, the “therapeutically effective amount” refers to a dose required to induce an antibody that can significantly reduce the probability of infection with human immunodeficiency virus type 1 or the severity of infection. The effective amount is determined by factors including the type and severity of a disease to be treated, the age and sex of a patient, sensitivity to a drug, an administration time, a route of administration, an excretion rate, a treatment period, and drugs to be used together and other factors well known in the pharmaceutical field, is an amount which may obtain the maximum effect without any side effects in consideration of all the above factors and may be easily determined by those skilled in the art.

(36) The dose of vaccine will depend on the patient's age, body weight and/or health status, as well as the route of administration. For example, a suitable dose may be, for example, 1 to 10.sup.9 CFU. In an exemplary embodiment, 10.sup.6 CFU is used. In the case of the strain according to the present invention, the expression level of an antigen, the antigen-presenting capacity, and the like are excellent, so it goes without saying that a smaller dose or a smaller dose compared to an existing strain vaccine may be used.

(37) As used herein, the term “prevention” refers to all actions that suppress AIDS and/or tuberculosis or delay the onset of the AIDS and/or tuberculosis by administering the vaccine composition according to the present invention.

(38) As used herein, the term “treatment” refers to all actions that ameliorate or beneficially change symptoms of AIDS and/or tuberculosis by administering the vaccine composition according to the present invention.

(39) In another aspect, the present invention relates to the vector disclosed on FIG. 2A used for the expression of p24 in the strain according to the present invention.

(40) In an exemplary embodiment, the vector is most preferably represented by a base sequence of SEQ ID NO: 4.

(41) In still another aspect, the present invention also relates to cells transformed with the vector. The cells include particularly Mycobacterium.

(42) Hereinafter, preferred examples for helping the understanding of the present invention will be suggested. However, the following examples are provided only to more easily understand the present invention, and the contents of the present invention are not limited by the following examples.

EXAMPLES

(43) [Experimental Method]

(44) 1. Mice and Immunization Procedures Female BALB/c mice (about 25 g, 7 weeks old) were purchased from Orient-Bio (Seoul, Korea) and used in the experiments at the age of 8 weeks. The mice were randomly divided into 4 groups consisting of 5 mice per group.

(45) For T cell proliferation assay, the p24 protein was injected through the tail vein into 2 mice (BALB/c)(30 μg/mouse), and 5 mice (BALB/c) were used to prepare bone marrow-derived dendritic cells (BMDCs) in each test.

(46) For vaccination test, the BALB/c mice were subcutaneously immunized twice (1×10.sup.6 CFU in 100 μl of PBS; 4 week intervals) at the bottom of the tail with a wild type, two recombinant BCG strains (rBCG-pAL-p24 and rBCG-pMyong2-p24) or a rSmeg-pMyong2-p24 strain. For negative control group, PBS was injected subcutaneously. Four weeks after the final immunization, mice were euthanized by CO.sub.2 inhalation at each time point, then blood and spleens of the mice were removed and used for an immunoassay such as IFN-γ ELISPOT, cytokine determination, serum antibody detection (5 mice/group), and CTL analysis (3 mice/group).

(47) Further, independent in vivo tests were conducted to compare differences in immune responses induced by p24 protein treatment and different bacterial numbers. In this case, BALB/c mice (group of 3) were subcutaneously injected twice at one week intervals with the p24 protein (30 μg/mouse) and different numbers of the rBCG-pMyong2-p24 strain (1×10.sup.6 and 1×10.sup.7 CFU). For negative control group, PBS was injected subcutaneously. One week after the final immunization, mice were euthanized by CO.sub.2 inhalation at each time point, blood and spleens of the mice were removed and used for an immunoassay such as IFN-γ ELISPOT, serum antibody detection, and CTL analysis.

(48) 2. Generation of rBCG Strains Expressing HIV-1 p24 Gag

(49) In order to generate three different types of rBCG strains expressing HIV-1 p24 Gag, that is, BCG with the pMyong2-p24 plasmid (rBCG-pMyong2-p24), BCG with the pAL-p24 plasmid (rBCG-pAL-p24), and BCG with the pMV306-p24 plasmid (rBCG-pMV306-p24), three constructed plasmids, that is, pMV306-p24, pAL-p24, and pMyong2-p24 were electroporated into a competent BCG strain (Tokyo 172) using a Gene Pulser II electroporation apparatus (Bio-Rad, Hercules, Calif., USA). Transformants were selected on Middlebrook 7H10 medium (Difco Laboratories, Detroit, Mich., USA) containing kanamycin (100 μg/ml) and OADC. Typically, transformant colonies were selected from plates, transferred to a 7H9 broth medium (Difco Laboratories, Detroit, Mich., USA) supplemented with 0.5% glycerol, 0.05% Tween-80, 10% ADC, and kanamycin, and cultured for 3 to 4 weeks. The growth rate of the rBCG strains was determined by optical density (OD) at 600 nm.

(50) 3. Production of p24 Protein from E. coli

(51) The recombinant p24 proteins was purified from E. coli as previously described with minor modification. For the expression and purification of a fusion protein, E. coli BL21 strains (RBC Bioscience, Taipei City, Taiwan) were transformed with pET23a-p24. Protein expression was induced by adding 0.4 mM isopropyl β-d-thiogalactoside (IPTG, Duchefa Biochemie, Haarlem, Netherlands). Bacterial cells were harvested and disrupted by sonication on ice for 10 minutes. The sonicated lysate were centrifuged at 1,600×g at 4° C. for 20 minutes, and pellets containing the p24 protein were resuspended in a binding buffer containing 4 M urea (Sigma Aldrich, St. Louis, Mo., USA). The proteins were purified using a Ni-NTA His binding resin (Merck, Darmstadt, Germany) and eluted with an elution buffer (300 mM NaCl, 50 mM sodium phosphate buffer, 250 mM imidazole) containing 4 M urea. Purified proteins were continuously dialyzed against the elution buffer to remove imidazole, urea, and residual salts. Purity of the p24 protein was estimated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE; 12% gel). The gel was visualized using Coomassie brilliant blue staining methods (FIG. 1).

(52) 4. Generation of Bone Marrow-Derived Dendritic Cells from Mice

(53) Bone marrow-derived dendritic cells were generated from the bone marrow (BM) of 8- to 12-week-old BALB/c mice as previously described. Briefly, the BM cells were flushed out of the femur and tibia using a serum-free Iscove's modified Eagle medium (IMDM; Gibco Invitrogen, UK). A single cell suspension was seeded at a concentration of 1×10.sup.6 cells per well in a 24-well plate in a final volume of 2 ml of complete IMDM supplemented with 10% FBS (Gibco Invitrogen), recombinant mouse GM-CSF (1.5 ng/ml; PeproTech, Rocky Hill, N.J., USA) and mouse IL-4 (1.5 ng/ml; PeproTech, USA), penicillin (100 units/ml; Gibco Invitrogen), streptomycin (100 μg/ml; Gibco Invitrogen), gentamicin (50 μg/ml; Gibco Invitrogen), L-glutamine (2 mM; Gibco Invitrogen), and β-mercaptoethanol (50 nM; Gibco Invitrogen). Half of the medium was replaced every other day with an equal volume of complete IMDM for 6 days. Five mice were used to prepare each experiment using BMDCs, and five 24-well plates were used for differentiating the BMDCs.

(54) 5. CFU Assay in Infected J774A.1 and BMDCs with rBCG Strains

(55) A murine macrophage cell line J774.1 (American Type Culture Collection, ATCC, TIB-67) was maintained at 37° C. and 5% CO.sub.2 in Dulbecco's modified Eagle's medium (DMEM; Thermo Scientific, Rockford, Ill., USA) supplemented with 10% (v/v) fetal bovine serum (FBS), 2 mM glutamine, and essential amino acids. BMDCs were generated from mouse BM as previously described and maintained at 37° C. and 5% CO.sub.2 in Iscove's modified Eagle medium (IMDM; Gibco Invitrogen, UK) supplemented with 10% FBS (Gibco Invitrogen), recombinant mouse GM-CSF (1.5 ng/ml; PeproTech, Rocky Hill, N.J., USA), mouse IL-4 (1.5 ng/ml; PeproTech, USA), penicillin (100 units/ml; Gibco Invitrogen), streptomycin (100 μg/ml; Gibco Invitrogen), gentamicin (50 μg/ml; Gibco Invitrogen), L-glutamine (2 mM; Gibco Invitrogen), and β-mercaptoethanol (50 nM; Gibco Invitrogen).

(56) The J774A.1 cells and BMDCs were infected with the rBCG strains, that is, rBCG-pMyong2-p24, -pAL-p24, and -pMV306-p24 and wild type BCG strains (10 M.O.I) (in triplicate) for 4 hours, followed by three washes with PBS and culturing for 24 hours with fresh media. After 24 hours, the infected cells were lysed with 0.5% Triton X-100. The cell lysate was diluted with PBS and plated onto Middlebrook 7H10 agar plates supplemented with OADC for enumeration of the colony forming units (CFUs). All infected groups were analyzed in triplicate in each experiment, and a total of two independent experiments were conducted.

(57) 6. Determination of p24 Gag Expression Levels in rBCG Strains

(58) To determine the p24 Gag expression levels in the rBCG strains, western blot and ELISA analyses were conducted. Briefly, pellets of cultured rBCG strains were suspended in B-PER buffer (Thermo Scientific, Rockford, Ill., USA) supplemented with lysozyme (100 μg/ml), DNase (5 U/ml), and a proteinase inhibitor. Then, the suspensions were sonicated for 5 minutes (pulse: 0.3 second, stop: 0.7 second) on ice and centrifuged at 13,000 rpm at 4° C. for 15 minutes. The same amount of protein in the aqueous phase was used for the western blot analysis. The expression levels of p24 in each rBCG strain were determined using a mouse anti-p24 monoclonal antibody (Abcam, Cambridge, USA; 1:1,000 dilution). Mycobacterial Hsp65 (Abcam, 1:1,000 dilution) was used as an internal control to confirm that the protein concentrations were equal in all samples. To assess the stable expression of p24, the p24 expression levels in the rBCG-pMyong2-p24 strain at various passage points (after 1, 4, 6, 8, 10, and 12 passages) were also determined. The passage process was conducted from plate to plate (7H10 agar plate with or without kanamycin), and the colonies obtained from each passage were cultured in a 7H9 broth medium for 3 weeks, and then each of the experiments was performed. Additionally, the same amount of protein was used for the detection of the p24 levels using a p24 ELISA kit (in triplicate wells) (ABL, Rockville, Md., USA) (as suggested by the manufacturer). All the groups were analyzed in two independent experiments.

(59) 7. Determination of p24 Gag Expression Levels in BMDCs and J774.1 Cells Infected with rBCG Strains

(60) For the rBCG infection, the J774.1 cells and BMDCs were seeded at 5 to 10×10.sup.5 cells per well (24-well plate, in triplicate) and cultured for 18 hours. The three different rBCG strains were infected into the cells at a multiplicity of infection (M.O.I) of 10. Also, different M.O.I (1 and 10 M.O.I) of the rBCG-pMyong2-p24 strain was infected into BMDCs to compare the difference in p24 expression by different M.O.I. The J774.1 cells and BMDCs were incubated for 4 hours to allow phagocytosis of the bacteria, and the extracellular bacteria were removed by washing with PBS three times. The infected J774.1 cells and BMDCs were incubated for 24 hours and/or 72 hours.

(61) In order to analyze the p24 expression in the cells, the total proteins in the cell pellets were prepared by suspension in RIPA lysis buffer and used for the determination of the p24 levels using the p24 ELISA kit (ABL) (in triplicate wells) according to the manufacturer's instructions. All the infected groups were analyzed in triplicate in each experiment, and a total of two independent experiments were conducted.

(62) 8. T Cell Proliferation Assay

(63) The following experiments were performed for T cell proliferation assay. Two mice were injected intravenously with the p24 protein (30 μg/mouse). After 7 days, the splenocytes were washed with ice-cold FACS buffer [PBS containing 1% bovine serum albumin (BSA) and 1 mM EDTA] and blocked on ice with a super block solution containing 10% rat serum (Sigma Aldrich), 10% goat serum (Gibco Invitrogen), 10% mouse serum (Sigma Aldrich), and 2.4G2 monoclonal antibodies (10 μg/ml; BD Biosciences, San Diego, Calif., USA) for 30 minutes. The cells were subsequently stained with BV421-conjugated anti-CD4 (Clone GK1.5, BD Biosciences) and PE-conjugated anti-CD8a (Clone 53-6.7, eBioscience, San Diego, Calif., USA) at 4° C. for 30 minutes and washed three times with ice-cold FACS buffer. The FACS AriaIII instrument (BD Biosciences) was used to sort the CD4 and CD8 T cell populations. Further, the day before co-culturing, immature BMDCs were infected with the wild type, two rBCGs (rBCG-pMyong2-p24 and -pAL-p24) or rSmeg-pMyong2-p24 strains at an M.O.I of 10 for 24 hours. Proliferation assays were conducted using a fluorescent cytoplasmic tracking dye CFSE (Invitrogen, Carlsbad, Calif., USA). The sorted CD4 and CD8 T cells were stained with 5 μM CFSE at 37° C. for 4 min and on ice for 4 minutes. And then, the CFSE-labeled T cells and infected BMDCs were co-cultured for 4 days.

(64) Four days after co-culturing T cells and infected BMDCs, the co-cultured cells (in triplicate wells) were blocked on ice with a super block solution for 30 minutes and stained with CD4 BV421-conjugated anti-CD4 (Clone GK1.5, BD Biosciences) and PE-conjugated anti-CD8a (Clone 53-6.7, eBioscience) at 4° C. for 30 minutes. The cell cycle profiles were determined using FACS LSRFortessa (BD Biosciences) and analyzed using FlowJo software (FIG. 4A). All the experiments were conducted in triplicate.

(65) 9. IL-2 ELISA

(66) The amounts of murine IL-2 in the co-cultured supernatants (in triplicate well) from the T cell proliferation assay were determined using ELISA according to the manufacturer's instructions (BioLegend, USA). All the experiments were conducted in duplicate.

(67) 10. Enzyme-Linked ImmunoSpot (ELISPOT) Assay

(68) Splenocytes obtained from mice (five mice/group) immunized with wild type and rBCG strains were used to conduct an ELISPOT assay as follows. In brief, 96-well ELISPOT plates (PVDF membrane) were coated with a mouse IFN-γ (3 μg/ml, clone: AN-18) capture antibody (BD-Biosciences, San Diego, Calif., USA) in PBS and incubated at 4° C. overnight. The capture antibody was discarded, and the plates were washed with PBS containing 0.05% Tween-20 (PBST) and PBS (3 times each), and the plates were blocked with 200 μl of RPMI 1640 medium including 10% FBS at 37° C. for 3 hours. After blocking, 5×10.sup.5 cells of splenocytes from vaccinated mice were loaded into each well. For each treatment group, the cells were stimulated in triplicate with 5 μg/ml of purified p24 antigen or medium alone in a total volume of 200 μl. The plate was incubated at 37° C. for 24 hours. The cells were stimulated with 5 ng/ml of phorbol 12-myristate 13-acetate (PMA) (Sigma-Aldrich, St. Louis, Mo., USA) and 500 ng/ml of ionomycin (Sigma-Aldrich) as a positive control. After washing with PBST and PBS (three times each), each well was treated with the biotin-labeled mouse IFN-γ (3 μg/ml, clone: XMG1.2) detection antibody (BD-Biosciences) and the plate was incubated at 4° C. overnight. The wells were washed again and horseradish peroxidase (HRP)-conjugated streptavidin was added to each well. The HRP reaction was developed using a 3-amino-9-ethylcarbazole substrate reagent set (BD-Biosciences). The number of spot forming units (SFUs) per well was automatically counted using an ELISPOT reader (AID ELISPOT reader, Strasburg, Germany). All the groups were analyzed in triplicate and two independent experiments were conducted.

(69) 11. Determination of Cytokine Production in Mice Immunized with rBCG Strains

(70) The splenocytes from the immunized mice (five mice/group) were adjusted to a concentration of 1×10.sup.6 cells/well (96-well microplate, 200 μl volume, in triplicate) in RPMI 1640 medium including 10% FBS, and purified p24 protein was added at a concentration of 5 μg/ml for the in vitro stimulation. The cells were cultured, and the supernatants were harvested for the IL-2 (BioLegend, San Diego, Calif., USA), IL-6 (eBioscience), and IFN-γ (BioLegend) cytokine determination using ELISA kits. All the groups were analyzed in triplicate and two independent experiments were conducted.

(71) 12. Serum Antibody Detection

(72) To detect the serum antibody ratio, serum samples were collected from the immunized mice (five mice/group) using the heart puncture method after euthanasia via hyperventilation of CO.sub.2. The 96-well plate was coated with purified p24 protein (5 μg/ml) in a 0.05 M carbonate-bicarbonate buffer (pH 9.6) at 4° C. overnight. The plate was washed three times with PBST and PBS and blocked with 5% bovine serum albumin (BSA in PBST) at room temperature (RT) for 1 hour. The serum samples were diluted at a ratio of 1:10 in PBS and 100 μl was added to each well (in triplicate). The plate was incubated at room temperature for 2 hours, washed three times with PBST and PBS, and incubated with biotinylated rat anti-mouse IgG2a, IgG1 (BD Biosciences, 1:1,000 dilution), and total IgG (eBioscience, 1:1,000 dilution) antibodies for 1 hour. Then, the plate was washed again and incubated with HRP conjugated streptavidin (eBioscience) at room temperature for 30 minutes. After the final washing step, all the wells were reacted with a BD OptEIA substrate (BD Biosciences) for 10 minutes, and then the reaction was stopped using 1 N H2504. The optical density (OD) was determined at a wavelength of 450 nm using a spectrometer.

(73) 13. Cytotoxic T Lymphocyte (CTL) Assay

(74) The induced CTL responses were determined as previously described with slight modifications. In brief, for the effector cells, the splenocytes obtained from the mice in each immunized group were pulsed using the major histocompatibility complex class I-restricted p24 peptide A9I (AMQMLKETI) (10 μg/ml; Peptron, Daejeon, Korea) and incubated with IL-2 (30 U/ml; PeproTech, Rocky Hill, N.J., USA) at 37° C. in a 5% CO.sub.2 incubator for 6 days. The target cells, that is, P815 cells (H-2d), were prepared by an incubation with the A9I peptide (10 μg/ml) for 2 hours followed by a co-culture of the effector and target cells. Cell cytotoxicity was evaluated using a lactate dehydrogenase (LDH) assay in U bottom 96-well plates according to the manufacturer's protocol (CytoTox 96 Non-Radioactive Cytotoxicity Assay; Promega, Madison, Wis., USA). In brief, the effector cells (splenocytes stimulated by antigens) were added to the target cells (p24 pulsed P815 cells) in triplicate at different effector/target (E/T) ratios (ranging from 10:1, 20:1 to 50:1) for 6 hours; then, the values of the LDH released from the cultured supernatants were detected using a spectrometer at 490 nm. The percentage of specific cell lysis was calculated using the following formula: [(Experimental−Effector spontaneous−Target spontaneous)/(Target maximum−Target spontaneous)]×100(%). All the groups were analyzed in triplicate and two independent experiments were conducted.

(75) 14. Statistical Analysis

(76) All presented data is expressed as the mean±SD. Student's t-test was used to compare the variance using Microsoft Excel software, and the differences were considered statistically significant at probability values less than 0.05.

EXAMPLES

Example 1. rBCG-pMyong2-p24 Strain Elicits Enhanced HIV-1 p24 Gag Expression in Bacteria and Infected Cells

(77) In the present invention, to examine the usefulness of a pMyong2 vector system in the preparation of rBCG for HIV-1 p24 Gag vaccination, three types of rBCG strains expressing p24, that is, rBCG-pMyong2-p24, rBCG-pAL-p24, and rBCG-pMV306-p24 were generated using different Mycobacterium-E. coli shuttle vectors, that is, pMyong2-TOPO, pAL-TOPO, and pMV306, respectively (FIG. 2A). The growth rates of the three rBCG strains were compared in 7H9 broth (including 100 μg/ml of kanamycin) for 30 days, and as a result, the rBCG and wild-type BCG strains showed a nearly identical growth rate (FIG. 2B). Additionally, to investigate the survival of these rBCG strains in macrophages and DCs, infected cells were lysed with 0.05% Triton X-100 (in PBS) and plated onto 7H10 agar plates. In both cells, the rBCG-pMyong2-p24 strain showed fewer colony forming units (CFUs) than the other strains (that is, rBCG-pAL-p24, -pMV306-p24, and wild-type BCG strains) likely due to the bacterial burden by the enhanced p24 expression (FIG. 2C).

(78) To compare the expression levels of p24 in the bacteria of the three rBCG strains, ELISA (FIG. 3A) and western blot (FIG. 3B) analyses for p24 after lysis of the cultured bacteria were performed. All rBCG strains could express the p24 protein. Similar to the rSmeg-pMyong2-p24 strain, the rBCG-pMyong2-p24 strain expressed approximately 2-fold or 3-fold higher levels of p24 than the strains in the other vector systems. rBCG-pAL-p24 produced a slightly higher level of p24 than rBCG-pMV306-p24 (FIGS. 3A and 3B).

(79) To assess the stable expression of p24, the expression levels of p24 in rBCG-pMyong2-p24 at various passage points on 7H10 agar plates with or without kanamycin were also determined by western blot analyses. The rBCG-pMyong2-p24 strain showed stable p24 expression even after 12 passages on the 7H10 agar plates with or without kanamycin (FIGS. 3D and 3F). Additionally, the expression levels of p24 in murine macrophages (J774A.1) and BMDCs infected with three rBCG strains were examined using ELISA. The trends observed were similar to those observed with the lysed rBCG strains (FIG. 3H).

(80) Further, to compare the p24 expression levels according to the different M.O.I, BMDCs were infected with different M.O.I (1 and 10 M.O.I) of rBCG-pAL-p24 and rBCG-pMyong2-p24 for 1 and 3 days. The results showed that an increased M.O.I of both strains appeared to have an effect of increasing p24 expression. However, as shown above, rBCG-pMyong2-p24 induced more p24 expression than the rBCG-pAL-p24 strain (FIG. 3I).

(81) Taken together, compared to the other two rBCG strains, that is, rBCG-pAL-p24 and rBCG-pMV306-p24, rBCG-pMyong2-p24 increased the production of p24 in infected antigen-presenting cells and bacteria.

Example 2. BMDCs Infected with rBCG-pMyong2-p24 Strain Elicits Enhanced T Cell Proliferation in Mice Immunized with HIV-1 p24 Gag

(82) In the present invention, to determine whether the rBCG-pMyong2-p24 showing enhanced p24 protein production could improve the T cell proliferation capacity, a T cell proliferation assay was conducted in BMDCs infected with four different strains, that is, a wild-type BCG (as a control), two types of rBCGs (rBCG-pMyong2-p24 and rBCG-pAL-p24), and rSmeg-pMyong2-p24, respectively using a CFSE dilution method via a mixed lymphocyte reaction (MLR). The rSmeg-pMyong2-p24 strain was also included to compare the capacity of inducing HIV-1 p24 Gag-specific immune responses between two different species using the same pMyong2 vector system, that is, rBCG-pMyong2-p24 and rSmeg-pMyong2-p24. A schematic of the T cell proliferation assay is illustrated in FIG. 4A.

(83) As a result, all BMDCs infected with the two rBCG and one rSmeg strains induced significantly higher levels of CD4 and CD8 T cell proliferation than the BMDCs that were not infected. In particular, the BMDCs infected with rBCG-pMyong2-p24 induced significantly higher levels of CD4 and CD8 T cell proliferation than those infected with the other two recombinant strains (rBCG-pAL-p24 and rSmeg-pMyong2-p24 strains) and the wild-type BCG strain. However, no significant difference in the proliferation of both CD4 and CD8 T cells was observed between the BMDCs infected with rBCG-pAL-p24 and those infected with rSmeg-pMyong2-p24 (FIGS. 4B and 4C). The comparison of the IL-2 levels in stimulated CD4 and CD8 T cells also showed trends that were similar to those observed in T cell proliferation assays (FIG. 4D).

Example 3. rBCG-pMyong2-p24 Strain Elicits Enhanced HIV-1 p24 Gag-Specific IFN-γ Spot Forming Cells (SFCs) in Mouse Spleens Generated by Subcutaneous Immunization

(84) To determine whether rBCG-pMyong2-p24 improved the T cell response after vaccination, splenocytes were isolated from the spleens of BALB/c mice (five mice/group) which were subcutaneously immunized with three different strains, that is, two types of rBCG strains (rBCG-pMyong2-p24 and -pAL-p24), rSmeg-pMyong2-p24 (FIG. 4A), and a wild type BCG strain (about 10.sup.6 CFU) as a control and assayed for HIV-1 p24 Gag-specific T cell responses using IFN-γ ELISPOT assays. The splenocytes from the mice that were subcutaneously immunized with the three recombinant strains showed significantly higher SFUs than those obtained from the mice that were immunized with the wild-type BCG strain. In particular, the splenocytes collected from the mice immunized with rBCG-pMyong2-p24 (987.78±195.11 SFUs/10.sup.6 splenocytes) induced significantly higher SFUs than those collected from the mice immunized with the other two strains, that is, rBCG-pAL-p24 (479.56±213.90 SFUs/10.sup.6 splenocytes) and rSmeg-pMyong2-p24 (647.00±151.01 SFUs/10.sup.6 splenocytes) (FIG. 5B). However, no significant difference was observed between the rBCG-pAL-24 and rSmeg-pMyong2-p24 strains in p24-specific IFN-γ SFUs from vaccinated mice (FIG. 5B).

(85) Taken together, data of the present invention indicated that rBCG-pMyong2-p24 elicited enhanced HIV-1 p24 Gag-specific production of IFN-γ, which is a Th-1 signature cytokine, suggesting its feasibility for enhancing vaccine efficacy by skewing the Th-1 type immune responses.

Example 4. rBCG-pMyong2-p24 Strain Elicits Enhanced Production of Th1 or Pro-Inflammatory Cytokines in Splenocytes Obtained from Vaccinated Mice

(86) The splenocytes (five mice/group) obtained 4 weeks after immunization twice with the rBCG strains and rSmeg-pMyong2-p24 (FIG. 5A) were stimulated in vitro in triplicate with purified p24 protein (5 μgimp, and the induced cytokine productions of IL-2, IFN-γ, and IL-6 in the cell culture supernatants were detected. For two Th1 type cytokines, that is, IL-2 and IFN-γ, and one pro-inflammatory cytokine, that is, IL-6, the rBCG-pMyong2-p24 strain produced higher levels of cytokines in splenocytes obtained from vaccinated mice at all time points (day 1 and 3) than the wild type or the other two recombinant strains (FIG. 5C and Table 1).

(87) TABLE-US-00001 TABLE 1 IL-2 (pg/ml) IFN-γ (pg/ml) IL-6 (pg/ml) Groups Day 1 Day 3 Day 1 Day 3 Day 1 Day 3 No treat  2.67 ± 0.09  1.29 ± 0.37 10.02 ± 1.41 11.32 ± 0.42 10.10 ± 1.16  9.92 ± 0.25 BCG  5.42 ± 0.24  9.42 ± 1.44 12.55 ± 0.44 10.95 ± 0.52 32.98 ± 1.91 33.22 ± 0.52 rBCG-pAL-p24 15.90 ± 0.06 29.53 ± 4.90 31.31 ± 1.12 29.75 ± 1.72 111.08 ± 22.47 107.28 ± 11.02 rBCG-pMyong2- 18.70 ± 3.44 33.86 ± 1.38 35.38 ± 2.02 56.50 ± 1.42 148.41 ± 22.76 166.26 ± 23.74 p24 rSmeg-pMyong2- 16.81 ± 0.41 29.84 ± 0.37 33.15 ± 1.80 46.70 ± 8.06 126.80 ± 3.76  155.76 ± 27.02 p24

Example 5. rBCG-pMyong2-p24 Strain Elicits HIV-1 p24 Gag-Specific Th1-Biased Humoral Response in Immunized Mice

(88) In the present invention, to determine whether rBCG-pMyong2-p24 elicits a Th1-biased humoral response in immunized mice, the levels of HIV-1 p24 Gag-specific IgG2a and IgG1, which are known markers of Th1 and Th2 responses, respectively, were analyzed. As shown in FIG. 6, the two rBCG and rSmeg-pMyong2-p24 strains elicited significantly higher levels of the IgG2a isotype than the wild type. Regarding the IgG1 isotype, the three recombinant strains induced similar levels of IgG1; however, the result did not reach statistical significance. In the case of total IgG, rBCG-pMyong2-p24 showed significantly higher levels of total IgG than the other two recombinant strains (that is, rBCG-pAL-p24 and rSmeg-pMyong2-p24) (FIG. 6).

(89) Taken together, a higher IgG2a/IgG1 ratio, in which a higher ratio indicates a more Th1-biased humoral immune response, was higher in the sera from the mice immunized with rBCG-pMyong2-p24 (1.03±0.02) than that in the sera from the mice immunized with the other strains (wild-type BCG=0.91±0.71; rBCG-pAL-p24=0.88±0.21; rSmeg-pMyong2-p24=1.01±0.17), and these results show that the rBCG-pMyong2-p24 strain can elicit an enhanced HIV-1 p24 Gag-specific Th1-biased humoral response in immunized mice.

Example 6. rBCG-pMyong2-p24 Strain Elicits Enhanced HIV-1 p24 Gag-Specific Cytotoxic T Lymphocyte Response in Immunized Mice

(90) In the present invention, to determine whether rBCG-pMyong2-p24 elicits an enhanced HIV-1 p24 Gag-specific cytotoxic T lymphocyte (CTL) response in immunized mice, the CTL activity in splenocytes from mice immunized with two rBCGs (that is, rBCG-pMyong2-p24 and -pAL-p24), rSmeg-pMyong2-p24, or wild-type BCG strains was evaluated via a LDH cytotoxicity assay. The immunization procedure is described in FIG. 5A. The P815 cells (H-2d) which were pulsed with the A9I peptide for 2 hours were used as the target cells, and the effector/target ratios were 10:1, 20:1, and 50:1 as previously described. As illustrated in FIG. 7, at an E:T ratio of 50:1, the CTLs in the mice immunized with rBCG-pMyong2-p24 could induce a significant higher level of HIV-1 p24 Gag-specific target cell lysis than those immunized with the other strains (FIG. 7). However, no significant difference was observed between the rBCG-pMyong2-p24 and rSmeg-pMyong2-p24 strains (FIG. 7).

Example 7. rBCG-pMyong2-p24 Strain Elicits Enhanced HIV-1 p24 Gag-Specific Humoral and Cell-Mediated Immune Responses in Immunized Mice, Compared to p24 Protein Vaccination

(91) In the present invention, to compare the p24-specific immune responses between the p24 protein and different CFUs of rBCG-pMyong2-p24 strains, an independent in vivo experiment was conducted with the following groups: i) PBS control, ii) p24 protein (30 μg/mouse) injection, iii) rBCG-pMyong2-p24 (1×10.sup.6 CFU) injection, and iv) rBCG-pMyong2-p24 (1×10.sup.7 CFU) injection (1 week intervals, twice subcutaneous injection) groups. The immunization procedure is described in the Experimental Method Section. After the final immunization, p24-specific IFN-γ ELISPOT, IgG subtype analyses, and CTL analyses were conducted. In the case of IFN-γ ELISPOT analysis, the p24-specific IFN-γ SFUs were increased in a CFU-dependent manner. However, splenocytes obtained from the p24 protein injected mice could not induce the p24-specific IFN-γ SFUs (FIG. 8A). Similarly, the p24-specific IgG2a antibodies in serum samples obtained from each immunized mouse were also increased in a CFU-dependent manner. However, the p24-specific IgG2a antibody in serum of the p24 protein injected mice showed lower levels than those of rBCG-pMyong2-p24 injected groups (FIG. 8B).

(92) Also, the p24-specific CTL responses were compared between the p24 protein and different CFUs of the rBCG-pMyong2-p24 strains. The data of the present specification showed that p24-specific CTL responses of rBCG-pMyong2-p24 were increased in a CFU-dependent manner and were always significantly higher than those of the p24 protein (FIG. 8C).

(93) Taken together, the data of the present specification shows that rBCG-pMyong2-p24 can elicit p24-specific Th1-biased cellular and humoral immune responses in a CFU-dependent manner and may have an advantage as an HIV-1 vaccine regimen, compared to a p24 protein vaccination module.

(94) The above-described description of the present invention is provided for illustrative purposes, and those skilled in the art to which the present invention pertains will understand that the present invention can be easily modified into other specific forms without changing the technical spirit or essential features of the present invention. Therefore, it should be understood that the above-described Examples are illustrative only in all aspects and are not restrictive.