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Cellular Immunity to Human Immunodeficiency Virus Type 1 (HIV‐1) Clades: Relevance to HIV‐1 Vaccine Trials in Uganda
Author(s) -
Huyen Cao,
Indu Mani,
Ronda Vincent,
Roy D. Mugerwa,
Peter Mugyenyi,
Phyllis J. Kanki,
Jerrold J. Ellner,
Bruce D. Walker
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315868
Subject(s) - clade , virology , biology , ctl* , immunogen , virus , hiv vaccine , immunology , antigen , human immunodeficiency virus (hiv) , vaccine trial , gene , antibody , genetics , phylogenetics , cd8 , monoclonal antibody
The first prophylactic human immunodeficiency virus type 1 (HIV-1) vaccine trial in Africa, with a clade B immunogen, is currently under way in Uganda, in a region where clades A and D are endemic. The use of a B clade vaccine is based on anticipated cross-recognition of endemic strains of HIV-1 in Uganda, but, in fact, little is known about the cytotoxic T lymphocyte (CTL) responses in that region. Seventeen HIV-1-infected volunteers from Kampala, Uganda, were studied to determine the immune responses elicited by natural infection with local HIV-1 strains. Despite the presence of broad cross-clade recognition, the CTL responses to the infecting viral clade were highest in most people. Recognition of nonendemic clade B antigens was similar to that of the coendemic local clade, and, in some instances, cross-recognition of clade B was greater. Nevertheless, the degree of cross-clade cellular responses we observed lends justification to the use of clade B-based immunogens in the current phase 1 vaccine trial in Uganda.

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