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1型人类免疫缺陷病毒感染中携带前病毒的CD4+细胞频率与CD8+细胞而非CD4+细胞的体外凋亡程度相关。

Frequency of provirus-bearing CD4+ cells in HIV type 1 infection correlates with extent of in vitro apoptosis of CD8+ but not of CD4+ cells.

作者信息

Carbonari M, Cibati M, Pesce A M, Sbarigia D, Grossi P, D'Offizi G, Luzi G, Fiorilli M

机构信息

Department of Clinical Medicine, University of Rome La Sapienza, Italy.

出版信息

AIDS Res Hum Retroviruses. 1995 Jul;11(7):789-94. doi: 10.1089/aid.1995.11.789.

Abstract

Lymphocytes from HIV-1-infected subjects undergo massive apoptosis when cultured in vitro, and this phenomenon might reflect pathogenetic mechanisms leading to immune dysfunction in vivo. However, (1) lymphocyte death is not restricted to CD4+ cells but seems to involve predominantly CD8+ cells, and (2) the same phenomenon occurs in other viral infections. Furthermore, it is not known whether a relationship exists between the HIV-1 burden and this type of cell death. In this work we sought to determine whether the HIV-1 provirus load correlates with the propensity to apoptosis of CD4+ and CD8+ cells. We studied 10 HIV-1-infected patients with CD4+ cell counts above 500/mm3 and free of concomitant infections. We correlated the frequency of HIV-1-infected CD4+ cells with the extent of culture-induced apoptosis as well as with the phenotype of the apoptotic lymphocytes. We found that the magnitude of apoptosis correlated with the frequency of HIV-1-infected CD4+ cells (p = 0.0007), and that increasing viral load and apoptosis were associated with a shift to the selective death of CD8+ cells. Our data support the view that, in addition to CD4+ cell killing, another immunopathogenic effect of HIV might be that of priming CD8+ cells to apoptosis. In vivo, this could eventually lead to the exhaustion of the cytotoxic T cell compartment.

摘要

来自HIV-1感染个体的淋巴细胞在体外培养时会发生大量凋亡,这种现象可能反映了导致体内免疫功能障碍的致病机制。然而,(1)淋巴细胞死亡并不局限于CD4+细胞,似乎主要涉及CD8+细胞,并且(2)在其他病毒感染中也会出现同样的现象。此外,尚不清楚HIV-1载量与这种细胞死亡类型之间是否存在关联。在这项研究中,我们试图确定HIV-1前病毒载量是否与CD4+和CD8+细胞的凋亡倾向相关。我们研究了10例CD4+细胞计数高于500/mm3且无合并感染的HIV-1感染患者。我们将HIV-1感染的CD4+细胞频率与培养诱导的凋亡程度以及凋亡淋巴细胞的表型进行了关联分析。我们发现凋亡程度与HIV-1感染的CD4+细胞频率相关(p = 0.0007),并且病毒载量增加和凋亡与CD8+细胞的选择性死亡转变相关。我们的数据支持这样一种观点,即除了杀伤CD4+细胞外,HIV的另一种免疫致病作用可能是促使CD8+细胞凋亡。在体内,这最终可能导致细胞毒性T细胞库的耗竭。

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