Wolthers K C, Miedema F
Dept of Clinical Viro-Immunology, Central Laboratory of the Netherlands Red Cross Blood Transfusion Service, Amsterdam.
Trends Microbiol. 1998 Apr;6(4):144-7. doi: 10.1016/s0966-842x(98)01233-5.
Telomere length analysis could be helpful in determining if exhaustion and replicative senescence are involved in HIV-1 pathogenesis. Evidence that CD8+ T cells have shorter telomeres may point towards an increased turnover of CD8+ T cells and exhaustion of the CD8+ T-cell responses in HIV-1 infection. In CD4+ T cells, the relationship between telomere length and turnover remains controversial; however, telomere length analysis argues against exhaustion of CD4+ T cells.
端粒长度分析可能有助于确定耗竭和复制性衰老是否参与了HIV-1发病机制。CD8+ T细胞端粒较短的证据可能表明HIV-1感染中CD8+ T细胞的更新增加以及CD8+ T细胞反应的耗竭。在CD4+ T细胞中,端粒长度与更新之间的关系仍存在争议;然而,端粒长度分析不支持CD4+ T细胞耗竭的观点。