首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Expression of HLA class I-specific inhibitory natural killer cell receptors in HIV-specific cytolytic T lymphocytes: Impairment of specific cytolytic functions
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Expression of HLA class I-specific inhibitory natural killer cell receptors in HIV-specific cytolytic T lymphocytes: Impairment of specific cytolytic functions

机译:HLA I类特异性抑制性自然杀伤细胞受体在HIV特异性溶细胞性T淋巴细胞中的表达:特异性溶细胞功能的损害

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摘要

Human T lymphocytes have been shown to express inhibitory natural killer cell receptors (NKR), which can down-regulate T cell antigen receptor-mediated T cell function, including cytolytic activity. In the present study, we demonstrate that CD3+NKR+ cells can be identified in HIV-infected patients. HIV-specific cytolytic activity was analyzed in five patients in whom autologous lymphoblastoid B cell lines could be derived as a source of autologous target cells. Phytohemagglutinin-activated T cell populations that had been cultured in interleukin 2 displayed HIV-specific cytotoxic T lymphocyte (CTL) activity against HIV env, gag, pol, and nef in 3 of 5 patients. Addition of anti-NKR mAb of IgM isotype could increase the specific CTL activity. Moreover, in one additional patient, HIV-specific CTL activity was undetectable; however, after addition of anti-NKR mAb such CTL activity appeared de novo. Similar results were obtained by analysis of CD3+NKR+ clones derived from two patients. These data provide direct evidence that CD3+NKR+ cells may include antigen (HIV)-specific CTLs and that mAb-mediated masking of inhibitory NKR may revert the down-regulation of CTL function.
机译:已显示人类T淋巴细胞表达抑制性自然杀伤细胞受体(NKR),该受体可下调T细胞抗原受体介导的T细胞功能,包括溶细胞活性。在本研究中,我们证明可以在HIV感染患者中鉴定出CD3 + NKR + 细胞。在五名患者中分析了HIV特异性的细胞溶解活性,在这些患者中可以衍生自体淋巴母细胞B细胞系作为自体靶细胞的来源。在白细胞介素2中培养的植物血凝素激活的T细胞群体在5名患者中有3名显示出针对HIV env,gag,pol和nef的HIV特异性细胞毒性T淋巴细胞(CTL)活性。 IgM同种型的抗NKR mAb的添加可以增加CTL的比活性。此外,在另一名患者中,无法检测到HIV特异的CTL活性。然而,在加入抗NKR mAb后,这种CTL活性从头出现。通过分析来自两名患者的CD3 + NKR + 克隆获得了相似的结果。这些数据提供了直接的证据,证明CD3 + NKR + 细胞可能包含抗原(HIV)特异的CTL,并且mAb介导的抑制性NKR掩蔽可能会逆转CD3 + NKR + 细胞CTL功能。

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