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首页> 外文期刊>The Journal of Experomental Medicine >Macrophage-dependent Apoptosis of CD4+ T Lymphocytes from HIV-infected Individuals Is Mediated by FasL and Tumor Necrosis Factor
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Macrophage-dependent Apoptosis of CD4+ T Lymphocytes from HIV-infected Individuals Is Mediated by FasL and Tumor Necrosis Factor

机译:FasL和肿瘤坏死因子介导的艾滋病毒感染者的CD4 + T淋巴细胞巨噬细胞依赖性凋亡。

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摘要

Apoptosis of bystander uninfected CD4+ T lymphocytes by neighboring HIV-infected cells is observed in cell culture and in lymphoid tissue of HIV-infected individuals. This study addresses whether antigen-presenting cells such as human macrophages mediate apoptosis of CD4+ T cells from HIV-infected individuals. Uninfected human macrophages, and to a larger degree, HIV-infected macrophages mediate apoptosis of T cells from HIV-infected, but not from uninfected control individuals. This macrophage-dependent killing targets CD4+, but not CD8+ T lymphocytes from HIV-infected individuals, and direct contact between macrophages and lymphocytes is required. Additional analyses indicated that the apoptosis-inducing ligands, FasL and tumor necrosis factor (TNF), mediate this macrophage-induced apoptosis of CD4+ T cells. These results support a role for macrophage-associated FasL and TNF in the selective depletion of CD4+ T cells in HIV-infected individuals.
机译:在HIV感染者的细胞培养物中和淋巴组织中观察到旁观者未感染的CD4 + T淋巴细胞被邻近的HIV感染细胞凋亡。这项研究解决了抗原呈递细胞(例如人类巨噬细胞)是否介导了HIV感染者的CD4 + T细胞凋亡。未感染的人类巨噬细胞,在更大程度上,HIV感染的巨噬细胞介导了HIV感染的T细胞的凋亡,但未感染的对照组却没有。这种巨噬细胞依赖性杀伤的目标是来自HIV感染者的CD4 +,而不是CD8 + T淋巴细胞,因此巨噬细胞和淋巴细胞之间需要直接接触。其他分析表明,凋亡诱导配体FasL和肿瘤坏死因子(TNF)介导了这种巨噬细胞诱导的CD4 + T细胞凋亡。这些结果支持巨噬细胞相关的FasL和TNF在HIV感染个体中CD4 + T细胞的选择性消耗中的作用。

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