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细胞毒性T淋巴细胞所表达的自然杀伤细胞样溶解活性与一种新的功能相关分子的表达有关。

The natural killer cell-like lytic activity expressed by cytolytic T lymphocytes is associated with the expression of a novel function-associated molecule.

作者信息

Harris D T, Jaso-Friedmann L, Devlin R B, Koren H S, Evans D L

机构信息

Department of Microbiology & Immunology, University of Arizona, Tucson 85721.

出版信息

Scand J Immunol. 1992 Mar;35(3):299-309. doi: 10.1111/j.1365-3083.1992.tb02862.x.

Abstract

Experiments were performed to analyse the natural killer cell (NK)-like cytotoxicity frequently expressed by human antigen-specific cytolytic T lymphocytes (CTL). To this end, several monoclonal antibodies (MoAbs) previously shown to identify a novel function-associated molecule (FAM) involved in human NK function were utilized. Flow cytometry revealed that these MoAbs reacted with the majority of human NK, but only with a subpopulation of CTL isolated from primary mixed lymphocyte cultures. Preincubation of CTL with the MoAbs inhibited the NK-like lysis of K562 targets. Experiments with anti-CD3 MoAb demonstrated that neither the NK-like cytotoxicity of CTL nor the lytic activity of NK were mediated by the CD3 complex. Expression of the novel FAM was found to develop in T-cell cultures at the time that NK-like cytotoxicity was observed. Repeated in vitro antigenic stimulation of CTL was shown to result in loss of NK-like cytotoxicity, as well as loss of the FAM on the CTL surface. Thus, NK-like cytotoxicity displayed by antigen-specific CTL appears to be mediated by a novel FAM that is identical to that structure found on NK.

摘要

开展实验以分析人类抗原特异性细胞毒性T淋巴细胞(CTL)频繁表达的自然杀伤细胞(NK)样细胞毒性。为此,利用了几种先前已证明可识别参与人类NK功能的新型功能相关分子(FAM)的单克隆抗体(MoAb)。流式细胞术显示,这些MoAb与大多数人类NK反应,但仅与从原发性混合淋巴细胞培养物中分离出的CTL亚群反应。用MoAb对CTL进行预孵育可抑制K562靶标的NK样裂解。抗CD3 MoAb实验表明,CTL的NK样细胞毒性和NK的裂解活性均不由CD3复合物介导。发现新型FAM的表达在观察到NK样细胞毒性时在T细胞培养物中出现。反复体外抗原刺激CTL可导致NK样细胞毒性丧失,以及CTL表面FAM丧失。因此,抗原特异性CTL显示的NK样细胞毒性似乎由一种与NK上发现的结构相同的新型FAM介导。

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