the evolutionary selective advantage of hiv-1 escape variants and the contribution of escape to the hla-associated risk of aids progressionhiv - 1逃脱变异的进化选择优势和逃避的贡献hla-associated艾滋病进展的风险.pdfVIP
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the evolutionary selective advantage of hiv-1 escape variants and the contribution of escape to the hla-associated risk of aids progressionhiv - 1逃脱变异的进化选择优势和逃避的贡献hla-associated艾滋病进展的风险
The Evolutionary Selective Advantage of HIV-1 Escape
Variants and the Contribution of Escape to the HLA-
Associated Risk of AIDS Progression
Becca Asquith*
Department of Immunology, Imperial College London, London, United Kingdom
Abstract
HIV-1 escape from surveillance by cytotoxic T lymphocytes (CTL) is thought to cause at least transient weakening of immune
control. However, the CTL response is highly adaptable and the long-term consequences of viral escape are not fully
understood. The objective of this study was to address the question ‘‘to what extent does HIV-1 escape from CTL contribute
to HLA-associated AIDS progression?’’ We combined an analysis of 21 escape events in longitudinally-studied HIV-1 infected
people with a population-level analysis of the functional CTL response in 150 subjects (by IFNg ELISpot) and an analysis of
the HIV-1 sequence database to quantify the contribution of escape to the HLA-associated rate of AIDS progression. We
found that CTL responses restricted by protective HLA class I alleles, which are associated with slow progression to AIDS,
recognised epitopes where escape variants had a weak evolutionary selective advantage (P = 0.008) and occurred
infrequently (P = 0.017). Epitopes presented by protective HLA class I alleles were more likely to elicit a CTL response
(P = 0.001) and less likely to contain sequence variation (P = 0.006). A third of between-individual variation in HLA-associated
disease risk was predicted by the selective advantage of escape variants: a doubling in the evolutionary selective advantage
was associated with a decrease in the AIDS-free period of 1.2 yrs. These results contribute to our understanding of what
makes a CTL response protective and why some individuals progress to AIDS more rapidly than others.
Citation: Asquith B (2008) The Evolut
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