Dittmer U, Petry H, Stahl-Hennig C, Nisslein T, Spring M, Luke W, Bodemer W, Kaup F J, Hunsmann G
Department for Virology and Immunology, German Primate Center, Göttingen.
J Gen Virol. 1996 Oct;77 ( Pt 10):2433-6. doi: 10.1099/0022-1317-77-10-2433.
Recent evidence suggests that T cell apoptosis could be involved in the pathogenesis of HIV infection. In addition, lymphocyte apoptosis has been described in SIV-infected macaques that developed simian AIDS. To investigate further the role of apoptosis in AIDS pathogenesis, we studied lymphocytes of HIV-2-infected cynomolgus macaques that did not develop simian AIDS. We compared apoptosis of lymphocytes from animals infected with non-pathogenic HIV-2 to that in macaques infected with pathogenic SIV. Unfractionated peripheral blood mononuclear cells of SIV- and HIV-2-infected macaques showed evidence of apoptosis by electron microscopy, flow cytometry (terminal dUTP nick end labelling) and visualization of DNA fragmentation. Between 30-50% apoptotic cells could be detected in SIV-infected animals, compared to approximately 30% in HIV-2-infected and 5-12% in uninfected monkeys. However, separation of PBMC into T cell subpopulations revealed striking differences in apoptosis between SIV- and HIV-2-infected macaques. In SIV-infected monkeys both CD4 and CD8 cells underwent apoptosis to a large extent. In contrast, in the HIV-2-infected macaques apoptosis was restricted to the CD8 cell compartment. The lack of apoptosis in CD4 cells of healthy HIV-2-infected macaques implies an important role for CD4 cell apoptosis in AIDS pathogenesis.
最近的证据表明,T细胞凋亡可能参与了HIV感染的发病机制。此外,在感染SIV并发展为猴艾滋病的猕猴中也发现了淋巴细胞凋亡。为了进一步研究凋亡在艾滋病发病机制中的作用,我们对未发展为猴艾滋病的HIV-2感染食蟹猴的淋巴细胞进行了研究。我们比较了感染非致病性HIV-2的动物与感染致病性SIV的猕猴淋巴细胞的凋亡情况。通过电子显微镜、流式细胞术(末端脱氧核苷酸转移酶介导的缺口末端标记法)和DNA片段化可视化分析,发现感染SIV和HIV-2的猕猴外周血单个核细胞均有凋亡迹象。在感染SIV 的动物中可检测到30%-50%的凋亡细胞,相比之下,感染HIV-2的动物中约为30%,未感染的猴子中为5%-12%。然而,将外周血单个核细胞分离为T细胞亚群后发现,感染SIV和HIV-2的猕猴在凋亡方面存在显著差异。在感染SIV的猕猴中,CD4和CD8细胞均大量发生凋亡。相比之下,在感染HIV-2的猕猴中,凋亡仅限于CD8细胞区室。健康的HIV-2感染猕猴的CD4细胞缺乏凋亡现象,这表明CD4细胞凋亡在艾滋病发病机制中起重要作用。