{"id":343325,"date":"2016-12-29T16:20:27","date_gmt":"2016-12-30T00:20:27","guid":{"rendered":"https:\/\/www.microsoft.com\/en-us\/research\/?post_type=msr-research-item&p=343325"},"modified":"2018-10-16T21:38:47","modified_gmt":"2018-10-17T04:38:47","slug":"early-immune-adaptation-hiv-1-revealed-population-level-approaches","status":"publish","type":"msr-research-item","link":"https:\/\/www.microsoft.com\/en-us\/research\/publication\/early-immune-adaptation-hiv-1-revealed-population-level-approaches\/","title":{"rendered":"Early immune adaptation in HIV-1 revealed by population-level approaches"},"content":{"rendered":"
\n

The reproducible nature of HIV-1 escape from HLA-restricted CD8+ T-cell responses allows the identification of HLA-associated viral polymorphisms \u201cat the population level\u201d \u2013 that is, via analysis of cross-sectional, linked HLA\/HIV-1 genotypes by statistical association. However, elucidating their timing of selection traditionally requires detailed longitudinal studies, which are challenging to undertake on a large scale. We investigate whether the extent and relative timecourse of immune-driven HIV adaptation can be inferred via comparative cross-sectional analysis of independent early and chronic infection cohorts.<\/p>\n<\/div>\n

<\/div>\n","protected":false},"excerpt":{"rendered":"

The reproducible nature of HIV-1 escape from HLA-restricted CD8+ T-cell responses allows the identification of HLA-associated viral polymorphisms \u201cat the population level\u201d \u2013 that is, via analysis of cross-sectional, linked HLA\/HIV-1 genotypes by statistical association. However, elucidating their timing of selection traditionally requires detailed longitudinal studies, which are challenging to undertake on a large scale. 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