Induction of Broad Cross-Subtype-Specific HIV-1 Immune Responses by a Novel Multivalent HIV-1 Peptide Vaccine in Cynomolgus Macaques
Author(s) -
Ali Azizi,
David E. Anderson,
José V. Torres,
Andrei Ogrel,
Masoud Ghorbani,
Catalina Soare,
Paul Sandstrom,
Jocelyne Fournier,
Francisco DíazMitoma
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.180.4.2174
Subject(s) - immunogenicity , hiv vaccine , immune system , heterologous , virology , biology , aids vaccines , immunology , immunity , human immunodeficiency virus (hiv) , antigen , macaque , potency , hiv antigens , simian immunodeficiency virus , peptide vaccine , antigenic variation , vaccine trial , epitope , genetics , viral disease , gene , in vitro , paleontology
One of the major obstacles in the design of an effective vaccine against HIV-1 is its antigenic variation, which results in viral escape from the immune system. Through a bioinformatics approach, we developed an innovative multivalent HIV-1 vaccine comprised of a pool of 176 lipidated and nonlipidated peptides representing variable regions of Env and Gag proteins. The potency and breadth of the candidate vaccine against a panel of HIV-1 subtypes was evaluated in nonhuman primate (cynomolgus macaques) and humanized mouse (HLA-A2.1) models. The results demonstrate strong immunogenicity with both breadth (humoral and cellular immunity) and depth (immune recognition of widely divergent viral sequences) against heterologous HIV-1 subtypes A-F.
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