Evidence of HIV-1 Adaptation to HLA-Restricted Immune Responses at a Population Level
Author(s) -
Corey Moore,
Mina John,
Ian James,
Frank Christiansen,
Campbell S. Witt,
S. Mallal
Publication year - 2002
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1069660
Subject(s) - human leukocyte antigen , biology , allele , immune system , population , immunology , hla b , immunity , hla b antigens , genetics , virology , viral load , antigen , virus , gene , medicine , environmental health
Antigen-specific T cell immunity is HLA-restricted. Human immunodeficiency virus-type 1 (HIV-1) mutations that allow escape from host immune responses may therefore be HLA allele-specific. We analyzed HIV-1 reverse transcriptase sequences from a large HLA-diverse population of HIV-1-infected individuals. Polymorphisms in HIV-1 were most evident at sites of least functional or structural constraint and frequently were associated with particular host HLA class I alleles. Absence of polymorphism was also HLA allele-specific. At a population level, the degree of HLA-associated selection in viral sequence was predictive of viral load. These results support a fundamental role for HLA-restricted immune responses in driving and shaping HIV-1 evolution in vivo.
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