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Home Drugs Modulation-of-cholesteryl-ester-transfer-protein-CETP-activity

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 Modulation of cholesteryl ester transfer protein (CETP) activity

Details
Inventors: Rittershaus, Charles W.; Thomas, Lawrence J.;
Assignee: Avant Immunotherapeutics, Inc. (Needham, MA)
Primary Examiner: Chan; Christina
Assistant Examiner: Belyavskyi; Michail
Attorney, Agent or Firm: Yankwich; Leon R. O'Brien; David G. Yankwich & Associates P.C.

This invention relates to peptides comprising a helper T cell epitope portion and a B cell epitope portion for eliciting an immune response against endogenous cholesteryl ester transfer protein (CETP) activity, to prevent or treat cardiovascular disease, such as atherosclerosis.

DETAILED DESCRIPTION The invention claimed is: 1.
A method for treating or preventing atherosclerosis in a human or animal comprising administering to said human or animal an antigenic vaccine peptide comprising a universal helper T cell epitope portion linked to a B cell epitope portion, wherein said B cell epitope portion comprises a B cell epitope of CETP.
2.
The method according to claim 1, wherein said helper T cell epitope portion comprises a helper T cell epitope derived from an antigenic peptide selected from the group consisting of tetanus toxoid, diphtheria toxoid, pertussis vaccine, Bacile Calmette-Guerin (BCG), polio vaccine, measles vaccine, mumps vaccine, rubella vaccine, purified protein derivative of tuberculin, keyhole limpet hemocyanin, hsp70, and combinations thereof.
3.
The method according to claim 1, wherein said B cell epitope portion of the antigenic vaccine peptide comprises 6 to 26 consecutive amino acids of the carboxyl terminal 26 amino acids of human cholesteryl ester transfer protein (SEQ ID NO:1).
4.
The method according to claim 3, wherein the vaccine peptide comprises the amino acid sequence of SEQ ID NO:2.
5.
The method according to claim 3, wherein the vaccine peptide comprises a dimer of the amino acid sequence of SEQ ID NO:2.
6.
The method according to claim 1, wherein the mode of said administration of said antigenic vaccine peptide is selected from the group consisting of intraperitoneal administration, interperitoneal administration, intramuscular injection, intravenous injection, subcutaneous injection, and oral administration.
7.
The method according to claim 6, wherein said administration is comprised of one primary dose of said antigenic vaccine peptide followed by one or more booster administrations of said vaccine peptide.
8.
The method according to claim 1, wherein said antigenic vaccine peptide is formulated with a pharmaceutically acceptable adjuvant.
9.
The method according to claim 8, wherein said pharmaceutically acceptable adjuvant is alum



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