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人类免疫缺陷病毒特异性细胞毒性T淋巴细胞中HLA I类特异性抑制性自然杀伤细胞受体的表达:特异性细胞溶解功能受损。

Expression of HLA class I-specific inhibitory natural killer cell receptors in HIV-specific cytolytic T lymphocytes: impairment of specific cytolytic functions.

作者信息

De Maria A, Ferraris A, Guastella M, Pilia S, Cantoni C, Polero L, Mingari M C, Bassetti D, Fauci A S, Moretta L

机构信息

Clinica delle Malattie Infettive I, Università degli Studi di Genova, 16132, Italy.

出版信息

Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10285-8. doi: 10.1073/pnas.94.19.10285.

Abstract

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.

摘要

已证明人类T淋巴细胞可表达抑制性自然杀伤细胞受体(NKR),其可下调T细胞抗原受体介导的T细胞功能,包括细胞溶解活性。在本研究中,我们证明在HIV感染患者中可鉴定出CD3+NKR+细胞。对五名患者的HIV特异性细胞溶解活性进行了分析,在这些患者中可获得自体淋巴母细胞B细胞系作为自体靶细胞来源。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名患者中的3名中表现出针对HIV env、gag、pol和nef的HIV特异性细胞毒性T淋巴细胞(CTL)活性。添加IgM同种型的抗NKR单克隆抗体可增加特异性CTL活性。此外,在另外一名患者中,未检测到HIV特异性CTL活性;然而,添加抗NKR单克隆抗体后,此类CTL活性重新出现。对来自两名患者的CD3+NKR+克隆进行分析也获得了类似结果。这些数据提供了直接证据,表明CD3+NKR+细胞可能包括抗原(HIV)特异性CTL,并且单克隆抗体介导的抑制性NKR掩盖可能会恢复CTL功能的下调。

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