首页> 美国卫生研究院文献>Immunology >Peripheral blood mononuclear cells of HIV-infected patients contain CD8 T cells that form conjugates with and kill HIV-infected autologous CD4 T cells
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Peripheral blood mononuclear cells of HIV-infected patients contain CD8 T cells that form conjugates with and kill HIV-infected autologous CD4 T cells

机译:HIV感染患者的外周血单个核细胞包含CD8 T细胞该CD8 T细胞与HI​​V感染的自体CD4 T细胞形成结合物并杀死它们

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摘要

Peripheral blood mononuclear cells (PBMC) of untreated, HIV-infected patients contain HIV-specific CD8 T cells as well as their corresponding targets, HIV-infected CD4 T cells. To determine if CD4 T-cell depletion in HIV-infected patients may result from autologous CD8–CD4 T-cell interaction, CD8 and CD4 T cells procured from PBMC of acute and chronic untreated HIV-infected patients were sorted and co-incubated. Formation of CD8-CD4 T-cell conjugates was observed by fluorescence microscopy. Apoptosis of CD4 T cells in conjugation was recorded by digitized images and was further observed and measured by FACS using Annexin staining. Perforin expression in the CD8 T cells was measured using intracellular monoclonal perforin antibody staining. HIV DNA in the conjugated CD4 T cells was detected by in situ PCR. We found that 6·1 ± 0·5% of CD4 T cells from acute HIV-infected patients and 3·0 ± 0·5% from chronic HIV-infected patients formed CD8–CD4 T-cell conjugates. Annexin binding and cell morphology typical of apoptosis were observed in the conjugated CD4 T cells. The majority of CD8 T cells that had conjugated to CD4 T cells expressed perforin. The conjugated CD4 T cells exhibited nuclear HIV DNA. CD8 T cells and HIV-infected CD4 T cells, both procured from the PBMC of untreated HIV-infected patients, form conjugates. Apoptotic lytic activity has been observed in the conjugated CD4 T cells. We propose that CD4 T-cell annihilation in HIV-infected patients results, at least in part, from the interactions of perforin-rich CD8 T cells with autologous, HIV-infected CD4 T cells.
机译:未经治疗的HIV感染患者的外周血单个核细胞(PBMC)包含HIV特异性CD8 T细胞以及其相应的靶标,HIV感染的CD4 T细胞。为了确定HIV感染患者的CD4 T细胞耗竭是否可能源于自体CD8–CD4 T细胞相互作用,对急性和慢性未经治疗的HIV感染患者的PBMC采购的CD8和CD4 T细胞进行了分类和共孵育。通过荧光显微镜观察到CD8-CD4 T细胞缀合物的形成。通过数字化图像记录缀合的CD4 T细胞的凋亡,并通过膜联蛋白染色通过FACS进一步观察和测量。使用细胞内单克隆穿孔素抗体染色来测量CD8 T细胞中穿孔素的表达。通过原位PCR检测缀合的CD4T细胞中的HIV DNA。我们发现,急性HIV感染患者的CD4 T细胞中有6·1±0·5%,慢性HIV感染患者的3·0±0·5%中有CD8–CD4 T细胞结合物。在缀合的CD4T细胞中观察到膜联蛋白结合和典型的细胞凋亡的细胞形态。与CD4 T细胞缀合的大多数CD8 T细胞表达穿孔素。缀合的CD4 T细胞显示出核HIV DNA。从未经治疗的HIV感染患者的PBMC获得的CD8 T细胞和HIV感染的CD4 T细胞形成结合物。在缀合的CD4T细胞中已经观察到凋亡的裂解活性。我们提出,HIV感染患者中的CD4 T细胞ni灭至少部分是由于富含穿孔素的CD8 T细胞与自体,HIV感染的CD4 T细胞的相互作用所致。

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