Document 0610 DOCN M9550610 TI Pimelautide or trimexautide as built-in adjuvants associated with an HIV-1-derived peptide: synthesis and in vivo induction of antibody and virus-specific cytotoxic T-lymphocyte-mediated response. DT 9505 AU Deprez B; Gras-Masse H; Martinon F; Gomard E; Levy JP; Tartar A; Faculte de Pharmacie, URA CNRS 1309, Institut Pasteur de Lille,; France. SO J Med Chem. 1995 Feb 3;38(3):459-65. Unique Identifier : AIDSLINE MED/95156422 AB Covalent association of lipopeptidic immunostimulants is known to improve the immunogenicity of short peptides. In this paper, we describe the synthesis of four analytically pure immunogens, prepared by two different strategies, in which a hexadecameric peptide (V3) derived from the principal neutralizing domain of HIV-1 envelope glycoprotein was associated with two different murein-derived lauroyl-peptides, Pimelautide (RP 44102), or Trimexautide (RP 56142). The in vivo immunogenicity of these compounds was evaluated according to two different criteria: the ability to elicit a cellular-T cytotoxic (CTL response) and the ability to stimulate antibody response. Our studies show that one of our compounds (TrxSucV3) was able to efficiently induce a relevant virus-specific CTL response, while another one (PimSucV3) was able to stimulate a strong antibody response to the linked peptide, or to a co-injected protein. These results suggest that both activities rely on different structure-activity relationships and that such a chemically defined model of peptide vaccines may be used to selectively stimulate subpopulations of immunocompetent cells. DE Adjuvants, Immunologic/*CHEMICAL SYNTHESIS Amino Acid Sequence Animal Cells, Cultured HIV Antibodies/BIOSYNTHESIS/IMMUNOLOGY HIV Envelope Protein gp120/*IMMUNOLOGY HIV-1/*IMMUNOLOGY Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred DBA Molecular Sequence Data Oligopeptides/*CHEMICAL SYNTHESIS/IMMUNOLOGY Peptide Fragments/*IMMUNOLOGY Pimelic Acids/*CHEMICAL SYNTHESIS/IMMUNOLOGY Support, Non-U.S. Gov't T-Lymphocytes, Cytotoxic/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).