Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, Wisconsin, USA.
J Virol. 2012 Jan;86(1):605-9. doi: 10.1128/JVI.05511-11. Epub 2011 Oct 19.
CD8+ T cell responses rapidly select viral variants during acute human immunodeficiency virus (HIV)/simian immunodeficiency virus (SIV) infection. We used pyrosequencing to examine variation within three SIV-derived epitopes (Gag₃₈₆₋₃₉₄GW9, Nef₁₀₃₋₁₁₁RM9, and Rev₅₉₋₆₈SP10) targeted by immunodominant CD8+ T cell responses in acutely infected Mauritian cynomolgus macaques. In animals recognizing all three epitopes, variation within Rev₅₉₋₆₈SP10 was associated with delayed accumulation of variants in Gag₃₈₆₋₃₉₄GW9 but had no effect on variation within Nef₁₀₃₋₁₁₁RM9. This demonstrates that the entire T cell repertoire, rather than a single T cell population, influences the timing of immune escape, thereby providing the first example of conditional CD8+ T cell escape in HIV/SIV infection.
CD8+ T 细胞反应在急性人类免疫缺陷病毒(HIV)/猴免疫缺陷病毒(SIV)感染期间迅速选择病毒变异株。我们使用焦磷酸测序来研究三个 SIV 衍生表位(Gag₃₈₆₋₃₉₄GW9、Nef₁₀₃₋₁₁₁RM9 和 Rev₅₉₋₆₈SP10)内的变异,这些表位是急性感染的毛里求斯食蟹猴中免疫优势 CD8+ T 细胞反应靶向的。在识别所有三个表位的动物中,Rev₅₉₋₆₈SP10 内的变异与 Gag₃₈₆₋₃₉₄GW9 中变异株的积累延迟有关,但对 Nef₁₀₃₋₁₁₁RM9 内的变异没有影响。这表明整个 T 细胞库,而不是单个 T 细胞群,影响免疫逃逸的时间,从而提供了 HIV/SIV 感染中条件性 CD8+ T 细胞逃逸的第一个例子。