PCSK9 peptide combination vaccine and method of use

Abstract

The present invention relates to a immunogen comprising at least two fragments of Proprotein convertase subtilisin/kexin type 9 (PCSK9), wherein at least two fragments comprise at least 8 consecutive amino acid residues of amino acid residues 150 to 170 and/or 205 to 225 of PCSK9 (SEQ ID NO:9).

Claims

1. An immunogen comprising at least two separate fragments of Proprotein convertase subtilisin/kexin type 9 (PCSK9), wherein a first fragment of said at least two fragments comprises at least 8 consecutive amino acid residues of amino acid residues 150 to 170, and wherein a second fragment of said at least two fragments comprises at least 8 consecutive amino acid residues of amino acid residues 205 to 225 of PCSK9 (SEQ ID NO: 9).

2. The immunogen of claim 1, wherein the first fragment of said at least two fragments comprises at least 9 consecutive amino acid residues of amino acid residues 150 to 170, and wherein the second fragment of said at least two fragments comprises at least 9 consecutive amino acid residues of amino acid residues 205 to 225 of PCSK9 (SEQ ID NO: 9).

3. The immunogen of claim 1, wherein the first fragment of said at least two fragments comprises at least 10 consecutive amino acid residues of amino acid residues 150 to 170, and wherein a second fragment of said at least two fragments comprises at least 10 consecutive amino acid residues of amino acid residues 205 to 225 of PCSK9 (SEQ ID NO: 9).

4. The immunogen of claim 1, wherein the first fragment of said at least two fragments comprises at least 15 consecutive amino acid residues of amino acid residues 150 to 170, and wherein the second fragment of said at least two fragments comprises at least 15 consecutive amino acid residues of amino acid residues 205 to 225 of PCSK9 (SEQ ID NO: 9).

5. The immunogen according to claim 1, wherein at least one fragment comprises at least 8 continuous residues of SIPWNLERITPPR (SEQ ID NO: 2), SIPWNLERITP (SEQ ID NO: 7) or SIPWNLERIT (SEQ ID NO: 8); and at least one other fragment consists of at least 8 contiguous residues of PEEDGTRFHRQASK (SEQ ID NO: 3), PEEDGTRFHRQA (SEQ ID NO: 4), EEDGTRFHRQASK (SEQ ID NO: 5), or EEDGTRFHRQAS (SEQ ID NO: 6).

6. The immunogen according to claim 1, wherein at least one fragment consists of at least 8 continuous residues of SIPWNLERITPPR (SEQ ID NO: 2), SIPWNLERITP (SEQ ID NO: 7) or SIPWNLERIT (SEQ ID NO: 8); and at least one other fragment consists of at least 8 contiguous residues of PEEDGTRFHRQASK (SEQ ID NO: 3), PEEDGTRFHRQA (SEQ ID NO: 4), EEDGTRFHRQASK (SEQ ID NO: 5), or EEDGTRFHRQAS (SEQ ID NO: 6).

7. The immunogen according to claim 1, wherein the immunogen comprises the following pairs of separate fragments: TABLE-US-00007 (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:3) PEEDGTRFHRQASK, (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:4) PEEDGTRFHRQA, (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:5) EEDGTRFHRQASK, (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:6) EEDGTRFHRQAS, (SEQIDNO:3) PEEDGTRFHRQASK and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:3) PEEDGTRFHRQASK and (SEQIDNO:8) SIPWNLERIT, (SEQIDNO:4) PEEDGTRFHRQA and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:4) PEEDGTRFHRQA and (SEQIDNO:8) SIPWNLERIT, (SEQIDNO:5) EEDGTRFHRQASK and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:5) EEDGTRFHRQASK and (SEQIDNO:8) SIPWNLERIT, (SEQIDNO:6) EEDGTRFHRQAS and (SEQIDNO:7) SIPWNLERITP or (SEQIDNO:6) EEDGTRFHRQAS and (SEQIDNO:8) SIPWNLERIT.

8. The immunogen according to claim 1, wherein the at least two fragments of PCSK9 comprise a cysteine residue at the C- and/or N-terminal end.

9. The immunogen according to claim 1, wherein the at least two fragments of PCSK9 are coupled to Keyhole limpet hemocyanin (KLH) or another pharmaceutically acceptable carrier.

10. The immunogen according to claim 1, wherein the at least two fragments of PCSK9 are formulated for intradermal, subcutaneous or intramuscular administration.

11. The immunogen according to claim 1, further comprising at least aluminum hydroxide or another adjuvant.

12. The immunogen according to claim 1, wherein said first fragment consists of the amino acid residues 150-170 of PCSK9 (SEQ ID NO: 9) and the second fragment consists of the amino acid residues 205-225 of PCSK9 (SEQ ID NO: 9).

13. The immunogen according to claim 1, wherein said first fragment consists of 8 to 20 amino acid residues of residues 150-170 of PCSK9 (SEQ ID NO: 9) and the second fragment consists of 8 to 20 amino acid residues of residues 205-225 of PCSK9 (SEQ ID NO: 9); wherein the first and/or second fragments optionally have a cysteine residue bound to their N and/or C-terminal(s).

14. The immunogen according to claim 1, wherein said first fragment consists of 8 to 20 amino acid residues of residues 150-170 of PCSK9 (SEQ ID NO: 9) and the second fragment consists of 8 to 20 amino acid residues of residues 205-225 of PCSK9 (SEQ ID NO: 9); wherein at least one of the first and/or second fragments has a cysteine residue bound to its N and/or C-terminal(s).

15. The immunogen according to claim 1, wherein said first fragment consists of 8 to 20 amino acid residues of residues 150-170 of PCSK9 (SEQ ID NO: 9) and the second fragment consists of 8 to 20 amino acid residues of residues 205-225 of PCSK9 (SEQ ID NO: 9); wherein at least one of the first and/or second fragments further comprises amino acid residues heterologous to PCSK9 (SEQ ID NO: 9).

16. The immunogen according to claim 1, wherein said first fragment consists of 8 to 20 amino acid residues of residues 153-165 of PCSK9 (SEQ ID NO: 9) and the second fragment consists of 8 to 20 amino acid residues of residues 209-222 of PCSK9 (SEQ ID NO: 9); wherein at least one of the first and/or second fragments have a cysteine residue bound to their N and/or C-terminal(s).

17. A process for treating and/or preventing at least one disorder caused by hyperlipidemia, hypercholesterolemia and/or atherosclerosis, comprising administering the immunogen of claim 1 to a subject in need thereof.

18. The process of claim 17, wherein the at least two peptide fragments of PCSK9 are administered in an amount of 0.1 ng to 10 mg per dose to the subject.

19. The process of claim 17 comprising administering said immunogen intradermally, subcutaneously, or intramuscularly.

20. A process for increasing an amount of LDL receptors or for reducing a mean value of LDLc and total cholesterol in a subject in need thereof comprising administering the immunogen of claim 1 to a subject in need thereof.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING

(1) The present invention is further illustrated in the following figures and examples without being restricted thereto.

(2) FIG. 1 shows the amount of low density lipoprotein receptor in liver lysates for peptides with Sequence ID No. 1 (irrelevant peptide control), 4, 5, 6, 7 and 8 and combination A (SEQ ID NO:4 and 7), B (SEQ ID NO:5 and 7), C (SEQ ID NO:5 and 8) and D (SEQ ID NO:6 and 8) compared to control animals.

(3) FIG. 2 shows the percent decrease of plasma levels of total cholesterol (n=5 mice per group) for peptides with Sequence ID No. 1 (irrelevant peptide control), 4, 5, 6, 7 and 8 and combination A (SEQ ID NO:4 and 7), B (SEQ ID NO:5 and 7), C (SEQ ID NO:5 and 8) and D (SEQ ID NO:6 and 8).

DETAILED DESCRIPTION OF THE INVENTION

(4) It turned surprisingly out that a vaccine comprising at least two different peptidic fragments of PCSK9 as defined above is able to increase the amount of LDL receptors much more efficiently compared to a vaccine comprising only one fragment of PCSK9. The administration of the vaccine of the present invention leads, for instance, to an increase in the levels of low density lipoprotein receptor in liver hepatocytes in vivo. As a consequence thereof, the mean values of LDLc and total cholesterol in blood plasma upon administration of vaccines decrease significantly. Therefore, the administration of a vaccine according to the present invention allows treating or preventing diseases caused by hyperlipidemia, hypercholesterolemia and/or atherosclerosis with a much higher efficiency and accuracy compared to the administration of the single peptides. In a preferred embodiment of the present invention all PCSK9 fragments of the vaccine of the present invention are derived from the PCSK9 fragments consisting of amino acid residues 150 to 170 and 205 to 225 of SEQ ID NO:9.

(5) The peptidic fragments used in the vaccine of the present invention comprise at least 8, preferably at least 9, more preferably at least 10, consecutive amino acid residues of amino acid residues 150 to 170, preferably of amino acid residues 153 to 165, and 205 to 225, preferably of amino acid residues 209 to 222, of PCSK9 (SEQ ID NO:9).

(6) TABLE-US-00001 SEQIDNO:9 (PCSK9aminoacidsequence): MGTVSSRRSWWPLPLLLLLLLLLGPAGARAQEDEDGDYEE LVLALRSEEDGLAEAPEHGTTATFHRCAKDPWRLPGTYVV VLKEETHLSQSERTARRLQAQAARRGYLTKILHVFHGLLP GFLVKMSGDLLELALKLPHVDYIEEDSSVFAQSIPWNLER ITPPRYRADEYQPPDGGSLVEVYLLDTSIQSDHREIEGRV MVTDFENVPEEDGTRFHRQASKCDSHGTHLAGVVSGRDAG VAKGASMRSLRVLNCQGKGTVSGTLIGLEFIRKSQLVQPV GPLVVLLPLAGGYSRVLNAACQRLARAGVVLVTAAGNFRD DACLYSPASAPEVITVGATNAQDQPVTLGTLGTNFGRCVD LFAPGEDIIGASSDCSTCFVSQSGTSQAAAHVAGIAAMML SAEPELTLAELRQRLIHFSAKDVINEAWFPEDQRVLTPNL VAALPPSTHGAGWQLFCRTVWSAHSGPTRMATAVARCAPD EELLSCSSFSRSGKRRGERMEAQGGKLVCRAHNAFGGEGV YAIARCCLLPQANCSVHTAPPAEASMGTRVHCHQQGHVLT GCSSHWEVEDLGTHKPPVLRPRGQPNQCVGHREASIHASC CHAPGLECKVKEHGIPAPQEQVTVACEEGWTLTGCSALPG TSHVLGAYAVDNTCVVRSRDVSTTGSTSEGAVTAVAICCR SRHLAQASQELQ

(7) The fragments derived from PCSK9 comprise or consist of preferably 8 to 20, more preferably 10 to 15, amino acid residues. According to a particularly preferred embodiment of the present invention the peptides derived from amino acid residues 150 to 170 of PCSK9 comprise 8 to 15, preferably 10 to 13, amino acid residues. The peptides derived from amino acid residues 205 to 225 of PCSK9 comprise 8 to 16, preferably 10 to 14, amino acid residues.

(8) The vaccine of the present invention is a combination of at least 2, preferably at least 3, more preferably at least 4, even more preferably at least 5, peptides derived from amino acid residues 150 to 170 and 205 to 225 of PCSK9 (SEQ ID NO:9). This combination comprises at least two sequences with different epitope origin.

(9) The peptides of the present invention can be chemically synthesized by methods which are well known in the art. Of course it is also possible to produce the peptides of the present invention using recombinant methods. The peptides can be produced in microorganisms such as bacteria, yeast or fungi, in eukaryotic cells such as mammalian or insect cells, or in a recombinant virus vector such as adenovirus, poxvirus, herpes virus, Simliki forest virus, baculovirus, bacteriophage, sindbis virus or Sendai virus. Suitable bacteria for producing the peptides include E. coli, B. subtilis or any other bacterium that is capable of expressing such peptides. Suitable yeast cells for expressing the peptides of the present invention include Saccharomyces cerevisiae, Schizosaccharomyces pombe, Candida, Pichia pastoris or any other yeast capable of expressing peptides. Corresponding means and methods are well known in the art. Also methods for isolating and purifying recombinantly produced peptides are well known in the art and include e.g. gel filtration, affinity chromatography, ion exchange chromatography etc.

(10) To facilitate isolation of the peptides of the present invention, fusion polypeptides may be made wherein the peptides are translationally fused (covalently linked) to a heterologous polypeptide which enables isolation by affinity chromatography. Typical heterologous polypeptides are His-Tag (e.g. His.sub.6; 6 histidine residues), GST-Tag (Glutathione-S-transferase) etc. The fusion polypeptide facilitates not only the purification of the peptides but can also prevent the degradation of the peptides during the purification steps. If it is desired to remove the heterologous polypeptide after purification the fusion polypeptide may comprise a cleavage site at the junction between the peptide and the heterologous polypeptide. The cleavage site may consist of an amino acid sequence that is cleaved with an enzyme specific for the amino acid sequence at the site (e.g. proteases).

(11) According to the present invention at least one fragment is derived from amino acid residues 150 to 170 and at least one fragment is derived from amino acid residues 205 to 225 of PCSK9 (SEQ ID NO:9).

(12) The vaccine of the present invention comprises PCSK9 fragments of different parts of the PCSK9 protein. Therefore, it is particularly preferred that at least one fragment is derived from one specific PCSK9 fragment, whereas at least one fragment is derived from another specific PCSK9 fragment.

(13) According to another preferred embodiment of the present invention the at least two fragments of PCSK9 are selected from the group consisting of peptides having amino acid sequence SIPWNLERITPPR (SEQ ID NO:2), PEEDGTRFHRQASK (SEQ ID NO:3), PEEDGTRFHRQA (SEQ ID NO:4), EEDGTRFHRQASK (SEQ ID NO:5), EEDGTRFHRQAS (SEQ ID NO:6), SIPWNLERITP (SEQ ID NO:7) and SIPWNLERIT (SEQ ID NO:8).

(14) The at least two fragments of PCSK9 may also consist of or comprise an amino acid sequence selected from the group consisting of FAQSIPWNLERITPPRYRAD (SEQ ID NO:10), FAQSIPWNLERITPPRYRA (SEQ ID NO:11), FAQSIPWNLERITPPRYR (SEQ ID NO:12), FAQSIPWNLERITPPRY (SEQ ID NO:13), FAQSIPWNLERITPPR (SEQ ID NO:14), FAQSIPWNLERITPP (SEQ ID NO:15), AQSIPWNLERITPPRYRAD (SEQ ID NO:16), QSIPWNLERITPPRYRAD (SEQ ID NO:17), SIPWNLERITPPRYRAD (SEQ ID NO:18), AQSIPWNLERITPPRYRA (SEQ ID NO:19), QSIPWNLERITPPRYRA (SEQ ID NO:20), SIPWNLERITPPRYRA (SEQ ID NO:21), AQSIPWNLERITPPRYR (SEQ ID NO:22), QSIPWNLERITPPRYR (SEQ ID NO:23), SIPWNLERITPPRYR (SEQ ID NO:24), QSIPWNLERITPPRY (SEQ ID NO:25), SIPWNLERITPPRY (SEQ ID NO:26), AQSIPWNLERITPPR (SEQ ID NO:27), QSIPWNLERITPPR (SEQ ID NO:28), SIPWNLERITPP (SEQ ID NO:29), ENVPEEDGTRFHRQASKCDS (SEQ ID NO:30), ENVPEEDGTRFHRQASKCD (SEQ ID NO:31), ENVPEEDGTRFHRQASKC (SEQ ID NO:32), ENVPEEDGTRFHRQASK (SEQ ID NO:33), NVPEEDGTRFHRQASKCDS (SEQ ID NO:34), VPEEDGTRFHRQASKCDS (SEQ ID NO:35), PEEDGTRFHRQASKCDS (SEQ ID NO:36), NVPEEDGTRFHRQASKCD (SEQ ID NO:37), VPEEDGTRFHRQASKCD (SEQ ID NO:38), PEEDGTRFHRQASKCD (SEQ ID NO:39), NVPEEDGTRFHRQASKC (SEQ ID NO:40), VPEEDGTRFHRQASKC (SEQ ID NO:41), PEEDGTRFHRQASKC (SEQ ID NO:42), NVPEEDGTRFHRQASK (SEQ ID NO:43), VPEEDGTRFHRQASK (SEQ ID NO:44), PEEDGTRFHRQAS (SEQ ID NO:45).

(15) The at least one fragment of PCSK9 has preferably an amino acid sequence selected from the group consisting of SIPWNLERITPPR (SEQ ID NO:2), SIPWNLERITP (SEQ ID NO:7) and SIPWNLERIT (SEQ ID NO:8) and at least one fragment of PCSK9 has an amino acid sequence selected from the group consisting of PEEDGTRFHRQASK (SEQ ID NO:3), PEEDGTRFHRQA (SEQ ID NO:4), EEDGTRFHRQASK (SEQ ID NO:5) and EEDGTRFHRQAS (SEQ ID NO:6).

(16) According to a preferred embodiment of the present invention the vaccine of the present invention comprises

(17) TABLE-US-00002 (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:3) PEEDGTRFHRQASK, (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:4) PEEDGTRFHRQA, (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:5) EEDGTRFHRQASK, (SEQIDNO:2) SIPWNLERITPPR and (SEQIDNO:6) EEDGTRFHRQAS, (SEQIDNO:3) PEEDGTRFHRQASK and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:3) PEEDGTRFHRQASK and (SEQIDNO:8) SIPWNLERIT, (SEQIDNO:4) PEEDGTRFHRQA and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:4) PEEDGTRFHRQA and (SEQIDNO:8) SIPWNLERIT, (SEQIDNO:5) EEDGTRFHRQASK and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:5) EEDGTRFHRQASK and (SEQIDNO:8) SIPWNLERIT, (SEQIDNO:6) EEDGTRFHRQAS and (SEQIDNO:7) SIPWNLERITP or (SEQIDNO:6) EEDGTRFHRQAS and (SEQIDNO:8) SIPWNLERIT, wherebyavaccinecomprising (SEQIDNO:4) PEEDGTRFHRQA and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:5) EEDGTRFHRQASK and (SEQIDNO:7) SIPWNLERITP, (SEQIDNO:5) EEDGTRFHRQASK and (SEQIDNO:8) SIPWNLERIT or (SEQIDNO:6) EEDGTRFHRQAS and (SEQIDNO:8) SIPWNLERITisparticularlypreferred.

(18) The at least two fragments of PCSK9 preferably comprise a cysteine residue at (bound to) the C- and/or N-terminal end.

(19) The provision of a cysteine residue at the N- and/or C-terminus of a peptide may facilitate its conjugation to a carrier, for instance, and/or may enhance the immunogenicity of the peptide.

(20) According to a preferred embodiment of the present invention the at least two fragments of PCSK9 (i.e. the at least two peptides derived from PCSK9) are coupled, individually or in combination, to a pharmaceutically acceptable carrier, preferably KLH (Keyhole Limpet Hemocyanin).

(21) According to a preferred embodiment of the present invention the at least two fragments of PCSK9 are coupled to a pharmaceutically acceptable carrier, preferably KLH (Keyhole Limpet Hemocyanin), tetanus toxoid, albumin-binding protein, hepatitis B core antigen, bovine serum albumin, a dendrimer (MAP), peptide linkers (or flanking regions) as well as the adjuvant substances described in Singh et al., Nat. Biotech. (1999), 1075-1081 (in particular those in Table 1 of that document), and O'Hagan et al., Nature Reviews, Drug Discovery (9) (2003), 727-735 (in particular the endogenous immuno-potentiating compounds and delivery systems described therein), or mixtures thereof. The conjugation chemistry (e.g. via heterobifunctional compounds such as GMBS and of course also others as described in Bioconjugate Techniques, Greg T. Hermanson) in this context can be selected from reactions known to the skilled man in the art. Moreover, the vaccine composition may be formulated with an adjuvant, preferably a low soluble aluminum composition, in particular aluminum hydroxide. Of course, also adjuvants like MF59 aluminum phosphate, calcium phosphate, cytokines (e.g., IL-2, IL-12, GM-CSF), saponins (e.g., QS21), MDP derivatives, CpG oligonucleotides, LPS, MPL, polyphosphazenes, emulsions (e.g., Freund's, SAF), liposomes, lipopeptides, virosomes, iscoms, cochleates, PLG microparticles, poloxamer particles, virus-like particles, heat-labile enterotoxin (LT), cholera toxin (CT), mutant toxins (e.g., LTK63 and LTR72), microparticles and/or polymerized liposomes may be used.

(22) The peptides of the present invention are preferably bound to the carrier or adjuvant via a linker, which is selected from the group consisting of NHS-poly (ethylene oxide) (PEO) (e.g. NHS-PEO.sub.4-maleimide).

(23) A vaccine which comprises a peptide of the present invention and the pharmaceutically acceptable carrier may be administered by any suitable mode of application, e.g. intradermally (i.d.), intraperitoneally (i.p.), intramuscularly (i.m.), intranasally, orally, subcutaneously (s.c.), etc. and in any suitable delivery device (O'Hagan et al., Nature Reviews, Drug Discovery 2 (9), (2003), 727-735). The compound of the present invention is preferably formulated for intradermal, subcutaneous or intramuscular administration. Means and methods for obtaining respective formulations are known to the person skilled in the art (see e.g. Handbook of Pharmaceutical Manufacturing Formulations, Sarfaraz Niazi, CRC Press Inc, 2004).

(24) Thus, the vaccine according to the present invention comprises at least two peptides which are preferably formulated for intradermal, subcutaneous or intramuscular administration.

(25) The at least two peptides/fragments in the vaccine of the present invention are preferably formulated with an adjuvant, preferably aluminum hydroxide.

(26) According to a preferred embodiment of the present invention the vaccine is used in the treatment and/or prevention of disorders caused by hyperlipidemia, hypercholesterolemia and/or atherosclerosis, preferably cardiovascular diseases, stroke or peripheral vascular diseases.

(27) As outlined, the above mentioned peptides and the combinations thereof are able to induce the formation of antibodies which are able to bind specifically PCSK9. The interaction of the antibodies with PCSK9 leads to the increase of low density lipoprotein receptor in liver hepatocytes in vivo and subsequent reduction of the plasma total cholesterol levels.

(28) The disease associated with atherosclerosis is preferably selected from the group consisting of peripheral arterial occlusive disease, coronary heart disease, apoplectic cerebral insultus and stroke.

(29) The terms diseases associated with hyperlipidemia, hypercholesterolemia and/or atherosclerosis and disorders caused by hyperlipidemia, hypercholesterolemia and/or atherosclerosis refer to diseases which are a consequence of hyperlipidemia, hypercholesterolemia and atherosclerosis. These diseases include among others peripheral arterial occlusive disease, coronary heart disease and apoplectic cerebral insultus (see e.g. Steinberg, D. J Lipid Res 46(2005):179-190 and Steinberg, D. J Lipid Res 47(2006):1339-1351).

(30) According to a preferred embodiment of the present invention the at least two fragments of PCSK9 are administered to an individual in an amount of 0.1 ng to 10 mg, preferably of 0.5 to 500 g, more preferably 1 to 100 g, per immunization. In a preferred embodiment these amounts refer to all fragments of PCSK9 present in the vaccine. In another preferred embodiment these amounts refer to each single fragment present in the vaccine. It is of course possible to provide a vaccine in which the specific fragments of PCSK9 are present in different or equal amounts. However, the peptide of the present invention may alternatively be administered to an individual in an amount of 0.1 ng to 10 mg, preferably 10 ng to 1 mg, in particular 100 ng to 300 g/kg body weight.

(31) The amount of peptides that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. The dose of the vaccine may vary according to factors such as the disease state, age, sex and weight of the individual, and the ability of antibody to elicit a desired response in the individual. Dosage regime may be adjusted to provide the optimum therapeutic response. For example, several divided doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation. The dose of the vaccine may also be varied to provide optimum preventative dose response depending upon the circumstances. For instance, the peptides and vaccine of the present invention may be administered to an individual at intervals of several days, one or two weeks or even months or years depending always on the level of antibodies directed to PCSK9.

(32) In a preferred embodiment of the present invention the peptide/vaccine is applied between 2 and 10, preferably between 2 and 7, even more preferably up to 5 and most preferably up to 4 times. This number of immunizations may lead to a basic immunisation. In a particularly preferred embodiment the time interval between the subsequent vaccinations is chosen to be between 2 weeks and 5 years, preferably between 1 month and up to 3 years, more preferably between 2 months and 1.5 years. An exemplified vaccination schedule may comprise 3 to 4 initial vaccinations over a period of 6 to 8 weeks and up to 6 months. Thereafter the vaccination may be repeated every two to ten years. The repeated administration of the peptide/vaccine of the present invention may maximize the final effect of a therapeutic vaccination.

(33) The vaccine of the present invention may also comprise antigens derived from other proteins which are also involved in the regulation of the LDL and/or HDL levels within a human body. For instance, the PCSK9 fragments of the present invention may be combined with epitopes derived from human CETP protein.

(34) Typically, the vaccine contains the peptides of the present invention in an amount of 0.5 to 500 g, preferably 1 to 100 g and alternatively from 0.1 ng to 10 mg, preferably 10 ng to 1 mg, in particular 100 ng to 100 g, or, alternatively, e.g. 100 fmol to 10 mol, preferably 10 mol to 1 mol, in particular 100 mol to 100 nmol. Typically, the vaccine may also contain auxiliary substances, e.g. buffers, stabilizers etc.

(35) According to a preferred embodiment of the present invention relates to the use of two or more peptides. According to the present invention for the manufacture of a vaccine for preventing and/or treating of atherosclerosis and diseases associated with atherosclerosis, wherein the disease associated with atherosclerosis is preferably selected from the group consisting of peripheral arterial occlusive disease, coronary heart disease, apoplectic cerebral insultus and stroke.

(36) Yet another aspect of the present invention relates to a method for treating an individual suffering or at risk to suffer from atherosclerosis or a disease associated with atherosclerosis in the course of which a peptide or vaccine according to the present invention is administered to said individual.

(37) Next to the vaccine of the present invention, the individual to be treated may receive also other active ingredients known to influence the LDL and/or HDL levels in humans and mammals such as statins, fibrates, nicotinic acid, cholesterol uptake inhibitor (e.g. ezetimibe), ApoA1 Milano, delipidated HDL, plant sterols. It is particularly preferred to administers to an individual the vaccine of the present invention together (i.e. at the same time, consecutively etc.) with statins.

Examples

Materials and Methods

(38) Vaccine:

(39) The peptides were conjugated via the heterobifunctional linker GMBS (4-Maleimidobutyric acid N-hydroxysuccinimide ester) to KLH (Keyhole Limpet Hemocyanin).

(40) 15 g of the peptides were suspended with aluminum hydroxide (end concentration of aluminum hydroxide was 0.2%). As buffer phosphate was used.

(41) TABLE-US-00003 TABLE1 Sequencesusedforthevaccineproduction Aminoacid sequence SequenceInformation SEQIDNO:1 RPETWIPNRSPIL irrelevant(control group) SEQIDNO:2 SIPWNLERITPPR aa153-165ofSEQID NO:9 SEQIDNO:3 PEEDGTRFHRQASK aa209-222ofSEQID NO:9 SEQIDNO:4 PEEDGTRFHRQA aa209-220ofSEQID NO:9 SEQIDNO:5 EEDGTRFHRQASK aa210-222ofSEQID NO:9 SEQIDNO:6 EEDGTRFHRQAS aa210-221ofSEQID NO:9 SEQIDNO:7 SIPWNLERITP aa153-163ofSEQID NO:9 SEQIDNO:8 SIPWNLERIT aa153-162ofSEQID NO:9 CombinationA PEEDGTRFHRQA+ aa209-220+ aa153- (SEQIDNO:4 SIPWNLERITP 163ofSEQIDNO:9 and7) CombinationB EEDGTRFHRQASK+ aa210-222+ aa153- (SEQIDNO:5 SIPWNLERITP 163ofSEQIDNO:9 and7) CombinationC EEDGTRFHRQASK+ aa210-222+ aa153- (SEQIDNO:5 SIPWNLERIT 162ofSEQIDNO:9 and8) CombinationD EEDGTRFHRQAS+ aa210-221+ aa153- (SEQIDNO:6 SIPWNLERIT 162ofSEQIDNO:9 and8)
Animal Experiments:

(42) 5 Balb/c mice were subcutaneously immunized. Mice had access to food and water ad libitum and were kept under a 12 h light/dark cycle. Age of mice at the beginning of experiments was usually 8 to 10 weeks.

(43) Mice were injected four times in 2 week intervals with 15 g of net peptide coupled to KLH and adsorbed to Alum as adjuvant in a volume of 1 ml in total via the s.c. route.

(44) Blood was taken approximately 2 weeks after the final injection.

(45) Protein ELISA:

(46) To determine the immunogenicity of the vaccines, 96-well Nunc-Maxisorb plates were coated with recombinant human PCSK9 protein. Unspecific binding was blocked by incubation with blocking buffer (1% BSA in PBS). Appropriate serum dilutions were added to the wells serially diluted 1:2 fold and incubated for approximately 1 hour at 37 C. On every ELISA plate a standard serum was included as internal control. Bound antibodies were detected by incubation with biotinylated goat anti-mouse IgG, followed by horseradish peroxidase coupled to Streptavidin. As substrate ABTS was added and the optical density (OD) at 405 nm was measured in a Microwell plate-reader. As negative control sera from the control group injected with an irrelevant peptide were analyzed. The titers were defined as the dilution of the serum where 50% of the ODmax in the assay are reached.

(47) Total Cholesterol Assay

(48) Total cholesterol was measured with the WAKO LabAssay Cholesterol Kit (Wako).

(49) LDLR Sandwich ELISA

(50) To determine the levels of low density lipoprotein receptor (LDLR) in murine liver, mice were sacrificed 2 weeks after the last vaccination. Liver tissue was isolated and protein extraction was done according to standard protocols.

(51) 96 well Nunc-Maxisorb plates were coated with mouse LDLR affinity purified goat polyclonal anti-LDLR antibody (R&D Systems). Unspecific binding was blocked by incubation with 1% BSA/PBS. Subsequently, the liver lysates were incubated for 3 h at room temperature to capture the murine LDLR. The detection of captured LDLR was done by chicken polyclonal anti-LDLR antibody (Abcam) followed by incubation with a secondary biotinylated goat anti-chicken IgG (Southern Biotech) and by streptavidin-HRP conjugate. Finally, TMB was used as a peroxidase chromogen substrate.

(52) The quantification of low density lipoprotein receptor was done by comparison to a standard calibration curve and was normalized to the total protein concentration of the lysates.

(53) The control group (irrelevant peptide control vaccination) has been set to 100%, and the levels of groups treated with anti-PCSK9 vaccines were compared to this control group.

Example 1

(54) Median protein titers against human PCSK9. (n=5 mice per group).

(55) TABLE-US-00004 Median Protein Sequence ID Titer OD max/2 seq 1 control 0 seq 4 45.000 seq 7 47.000 seq 5 14.000 seq 7 47.000 seq 5 14.000 seq 8 31.000 seq 6 13.000 seq 8 31.000

Example 2

(56) Mean values in mg/dL and percentage of decrease of total cholesterol. (n=5 mice per group).

(57) TABLE-US-00005 % TC decrease Mean Values compared to Sequence ID (mg/dl) Stdv control group Combination A 1 (control) 98 9 4 88 12 10 7 78 4 20 4 + 7 71 5 28 Combination B 1 (control) 86 9 5 61 7 29 7 64 5 26 5 + 7 51 1 41 Combination C 1 (control) 83 7 5 60 8 28 8 55 3 34 5 + 8 47 7 43 Combination D 1 (control) 83 7 6 65 4 22 8 55 3 34 6 + 8 48 4 42

Example 3

(58) Amount of low density lipoprotein receptor in mouse liver in vivo (n=5 mice per group), compared to the control group.

(59) TABLE-US-00006 Sequence ID % LDLR Stdv Combination A 1 (control) 100 8 4 130 8 7 148 12 4 + 7 212 24 Combination B 1 (control) 100 19 5 140 6 7 140 14 5 + 7 202 18 Combination C 1 (control) 100 13 5 135 12 8 143 17 5 + 8 212 21 Combination D 1 (control) 100 22 6 116 27 8 125 14 6 + 8 187 30