Seki Sayuri, Kawada Miki, Takeda Akiko, Igarashi Hiroko, Sata Tetsutaro, Matano Tetsuro
International Research Center for Infectious Diseases, The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
J Virol. 2008 May;82(10):5093-8. doi: 10.1128/JVI.02607-07. Epub 2008 Mar 12.
Cytotoxic T-lymphocyte (CTL) responses frequently select for immunodeficiency virus mutations that result in escape from CTL recognition with viral fitness costs. The replication in vivo of such viruses carrying not single but multiple escape mutations in the absence of the CTL pressure has remained undetermined. Here, we have examined the replication of simian immunodeficiency virus (SIV) with five gag mutations selected in a macaque possessing the major histocompatibility complex haplotype 90-120-Ia after its transmission into 90-120-Ia-negative macaques. Our results showed that even such a "crippled" SIV infection can result in persistent viral replication, multiple reversions, and AIDS progression.
细胞毒性T淋巴细胞(CTL)反应常常会选择免疫缺陷病毒的突变,这些突变会导致病毒逃避CTL识别,但会付出病毒适应性代价。在没有CTL压力的情况下,携带多个而非单个逃逸突变的此类病毒在体内的复制情况仍未确定。在此,我们研究了在一只拥有主要组织相容性复合体单倍型90 - 120 - Ia的猕猴中选择出的带有五个gag突变的猿猴免疫缺陷病毒(SIV),将其接种到90 - 120 - Ia阴性的猕猴体内后的复制情况。我们的结果表明,即使是这种“有缺陷的”SIV感染也会导致病毒持续复制、多次回复突变以及艾滋病进展。