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在感染1型人类免疫缺陷病毒的黑猩猩中,CD4 + T细胞的丧失与淋巴细胞凋亡增加有关。

Loss of CD4+ T cells in human immunodeficiency virus type 1-infected chimpanzees is associated with increased lymphocyte apoptosis.

作者信息

Davis I C, Girard M, Fultz P N

机构信息

Department of Comparative Medicine, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.

出版信息

J Virol. 1998 Jun;72(6):4623-32. doi: 10.1128/JVI.72.6.4623-4632.1998.

Abstract

Supportive evidence that apoptosis contributes to loss of CD4+ lymphocytes in human immunodeficiency virus type 1 (HIV-1)-infected humans comes from an apparent lack of abnormal apoptosis in apathogenic lentivirus infections of nonhuman primates, including HIV-1 infection of chimpanzees. Two female chimpanzees were inoculated, one cervically and the other intravenously, with HIV-1 derived from the LAI/LAV-1b strain, which was isolated from a chimpanzee infected with the virus for 8 years. Within 6 weeks of infection, both recipient chimpanzees developed a progressive loss of CD4+ T cells which correlated with persistently high viral burdens and increased levels of CD4+ T-cell apoptosis both in vitro and in vivo. Lymph nodes from both animals also revealed evidence of immune hyperactivation. Intermediate levels of T-cell apoptosis in both peripheral blood and lymph nodes were seen in a third chimpanzee that had been infected with the LAI/LAV-1b strain for 9 years; this animal has maintained depressed CD4/CD8 T-cell ratios for the last 3 years. Similar analyses of cells from 4 uninfected animals and 10 other HIV-1-infected chimpanzees without loss of CD4+ cells revealed no difference in levels of apoptosis in these two control groups. These results demonstrate a correlation between immune hyperactivation, T-cell apoptosis, and chronic loss of CD4+ T cells in HIV-1-infected chimpanzees, providing additional evidence that apoptosis is an important factor in T-cell loss in AIDS. Furthermore, the results show that some HIV-1 strains are pathogenic for chimpanzees and that this species is not inherently resistant to HIV-1-induced disease.

摘要

细胞凋亡导致人类免疫缺陷病毒1型(HIV-1)感染的人类体内CD4+淋巴细胞减少,这一观点的支持证据来自于非人灵长类动物感染无致病性慢病毒时明显缺乏异常细胞凋亡,包括黑猩猩感染HIV-1。给两只雌性黑猩猩接种了来自LAI/LAV-1b毒株的HIV-1,一只通过宫颈接种,另一只通过静脉接种,该毒株是从一只感染该病毒8年的黑猩猩身上分离出来的。在感染后的6周内,两只受体黑猩猩的CD4+T细胞逐渐减少,这与持续的高病毒载量以及体外和体内CD4+T细胞凋亡水平的增加相关。两只动物的淋巴结也显示出免疫激活过度的迹象。第三只感染LAI/LAV-1b毒株9年的黑猩猩,其外周血和淋巴结中的T细胞凋亡水平处于中等程度;在过去3年里,这只动物的CD4/CD8 T细胞比值一直较低。对4只未感染动物和10只其他未出现CD4+细胞减少的HIV-1感染黑猩猩的细胞进行的类似分析显示,这两个对照组的细胞凋亡水平没有差异。这些结果表明,在HIV-1感染的黑猩猩中,免疫激活过度、T细胞凋亡与CD4+T细胞的慢性减少之间存在关联,为细胞凋亡是艾滋病中T细胞减少的重要因素提供了额外证据。此外,结果表明一些HIV-1毒株对黑猩猩具有致病性,并且该物种并非天生对HIV-1诱导的疾病具有抗性。

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