Jaworowski A, Crowe S M
AIDS Pathogenesis Research Unit, Macfarlane Burnet Centre for Medical Research, National Centre for HIV Virology Research, Fairfield, Victoria, Australia.
Immunol Cell Biol. 1999 Feb;77(1):90-8. doi: 10.1046/j.1440-1711.1999.00798.x.
The central pathogenic feature of AIDS is the dramatic loss of CD4+ lymphocytes. Despite more than a decade of intense research, the exact mechanism by which HIV causes this is still not understood. A major model for T cell depletion, proposed originally by Ameison and Capron in a report published in 1991, is that HIV sensitizes CD4+ T cells for activation-induced apoptosis. The apoptotic model of T cell depletion is discussed, and experiments that address the questions of whether apoptosis is restricted to infected cells or 'bystander' T cells, and whether T cell apoptosis requires participation of separate HIV-infected haematopoietic cell populations, are reviewed.
艾滋病的核心致病特征是CD4+淋巴细胞显著减少。尽管经过了十多年的深入研究,HIV导致这种情况的确切机制仍未明确。1991年艾梅森和卡普隆在一份报告中首次提出的一种主要的T细胞耗竭模型认为,HIV使CD4+T细胞对激活诱导的凋亡敏感。本文讨论了T细胞耗竭的凋亡模型,并综述了一些实验,这些实验探讨了凋亡是否仅限于受感染细胞或“旁观者”T细胞的问题,以及T细胞凋亡是否需要不同的HIV感染造血细胞群体参与的问题。