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克隆化人细胞毒性T淋巴细胞产生的细胞毒性淋巴因子。I. 抗原特异性及自然杀伤样细胞毒性T淋巴细胞产生的细胞毒素与经典淋巴毒素不同。

Cytotoxic lymphokines produced by cloned human cytotoxic T lymphocytes. I. Cytotoxins produced by antigen-specific and natural killer-like CTL are dissimilar to classical lymphotoxins.

作者信息

Green L M, Stern M L, Haviland D L, Mills B J, Ware C F

出版信息

J Immunol. 1985 Dec;135(6):4034-43.

PMID:2415596
Abstract

Several cloned lines of IL 2-dependent human T cells derived from alloantigen, mitogen, or IL 2-stimulated peripheral blood lymphocytes were examined for their surface marker expression, cytolytic activity in a 51Cr-release assay, and capacity to release cytotoxic lymphokines. Thirty cell lines exhibiting either antigen-specific natural killer cell activity or lectin-dependent killer cell function, which expressed either the CD4 or CD8 surface differentiation markers, were capable of producing cytotoxin(s) in response to the lectins phytohemagglutinin and concanavalin A. Cytotoxin activity was detected on the murine L929 target cell in a 16-hr cytotoxicity assay. In contrast, several nonlytic T cell tumor lines failed to produce a soluble cytotoxin. Antibodies capable of neutralizing human alpha-lymphotoxin were completely ineffective in inhibiting the cytotoxin(s) produced by any of the cytotoxic T lymphocytes (CTL) cell lines. Comparative gel filtration and HPLC hydrophobic chromatography of alpha-lymphotoxin and CTL toxin produced by the CTL-830.B2 clone revealed significant differences in their elution profiles. The CTL-produced toxin and alpha-lymphotoxin exhibited similar kinetics of lysis of the L929 target cells, with 50% target cell lysis occurring at 10 hr. These data indicate human CTL produce a cytotoxin(s) antigenically distinct from alpha-lymphotoxin and imply that human cytolytic effector T cells are not the cellular source for the production of human alpha-lymphotoxin. The relationship of alpha-lymphotoxin and CTL toxin production was investigated in unseparated peripheral blood mononuclear cells stimulated with lectins or IL 2 for 1 and 5 days. Anti-alpha-lymphotoxin antibodies were capable of neutralizing only 30 to 50% of the cytotoxic activity in 24-hr supernatants. Cytotoxic activity in supernatants harvested after 120 hr stimulation with PHA or Con A was neutralized 70 to 100%, whereas the toxin(s) released from IL 2-stimulated lymphocytes was only neutralized 30%. These data suggest the observed heterogeneity of cytotoxic lymphokines produced by unseparated mononuclear cells depends in part on the subpopulations of effector cells responding to a given stimulus and the capacity of different subpopulations to produce distinct cytotoxins.

摘要

对从同种异体抗原、丝裂原或白细胞介素2(IL 2)刺激的外周血淋巴细胞中获得的几株依赖IL 2的人T细胞克隆系进行了检测,分析其表面标志物表达、在51铬释放试验中的细胞溶解活性以及释放细胞毒性淋巴因子的能力。30株表现出抗原特异性自然杀伤细胞活性或凝集素依赖性杀伤细胞功能的细胞系,表达CD4或CD8表面分化标志物,能够在响应植物血凝素和刀豆球蛋白A这两种凝集素时产生细胞毒素。在16小时的细胞毒性试验中,在小鼠L929靶细胞上检测到细胞毒素活性。相比之下,几株非溶细胞性T细胞肿瘤系未能产生可溶性细胞毒素。能够中和人α-淋巴毒素的抗体在抑制任何细胞毒性T淋巴细胞(CTL)细胞系产生的细胞毒素方面完全无效。对CTL-830.B2克隆产生的α-淋巴毒素和CTL毒素进行比较凝胶过滤和高效液相色谱疏水色谱分析,结果显示它们的洗脱图谱存在显著差异。CTL产生的毒素和α-淋巴毒素对L929靶细胞的裂解动力学相似,50%的靶细胞裂解发生在10小时。这些数据表明人CTL产生一种抗原性与α-淋巴毒素不同的细胞毒素,这意味着人溶细胞效应T细胞不是人α-淋巴毒素的细胞产生源。在用凝集素或IL 2刺激1天和5天的未分离外周血单个核细胞中研究了α-淋巴毒素和CTL毒素产生之间的关系。抗α-淋巴毒素抗体仅能中和24小时培养上清液中30%至50%的细胞毒性活性。在用PHA或Con A刺激120小时后收获的上清液中的细胞毒性活性被中和70%至100%,而从IL 2刺激的淋巴细胞中释放的毒素仅被中和30%。这些数据表明,未分离的单个核细胞产生的细胞毒性淋巴因子的异质性部分取决于对给定刺激作出反应的效应细胞亚群以及不同亚群产生不同细胞毒素的能力。

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