Document 0716 DOCN M9620716 TI A macromolecular multicomponent peptide vaccine prepared using the glutaraldehyde conjugation method with strong immunogenicity for HIV-1. DT 9602 AU Hamajima K; Bukawa H; Fukushima J; Kawamoto S; Kaneko T; Sekigawa K; Tanaka S; Tsukuda M; Okuda K; Department of Bacteriology, Yokohama City University School of; Medicine, Japan. SO Clin Immunol Immunopathol. 1995 Dec;77(3):374-9. Unique Identifier : AIDSLINE MED/96080367 AB The immunogenicity of a newly constructed macromolecular multicomponent peptide vaccine candidate against human immunodeficiency virus type 1 (HIV-1) was compared with that of previously reported vaccine candidates. This vaccine candidate is composed of a macromolecular multicomponent peptide complex consisting of three V3 region peptides, one Gag region peptide, and CD4-binding site peptide and was constructed using the multiple-antigen peptide and glutaraldehyde methods. Sera from rabbits immunized with this newly constructed vaccine showed strong antibody titers against each constituent peptide antigen. Furthermore, these antibodies exhibited strong neutralizing and antifusion activity toward HIV-1IIB, HIV-1MN, and fresh isolates from Japanese HIV-seropositive individuals. These results show that this new vaccine candidate has the capacity to induce strong, polyvalent immunogenicity and therefore may prove to be a powerful peptide vaccine against HIV-1 infection. DE Amino Acid Sequence Animal AIDS Vaccines/*IMMUNOLOGY Enzyme-Linked Immunosorbent Assay Glutaral/*PHARMACOLOGY Human HIV Antibodies/BIOSYNTHESIS HIV Antigens/CHEMISTRY/IMMUNOLOGY/PHARMACOLOGY HIV-1/*IMMUNOLOGY Molecular Sequence Data Neutralization Tests Rabbits Support, Non-U.S. Gov't Vaccines, Synthetic/CHEMISTRY/DRUG EFFECTS/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).