Suppr超能文献

H-2K/H-2D以及Mls和I区相关抗原刺激参与细胞毒性T淋巴细胞生成的辅助因子。

H-2K/H-2D and Mls and I region-associated antigens stimulate helper factor(s) involved in the generation of cytotoxic T lymphocytes.

作者信息

Scott J W, Ponzio N M, Orosz C G, Finke J H

出版信息

J Immunol. 1980 May;124(5):2378-83.

PMID:6444971
Abstract

This study examines the antigen that stimulate production or release of a soluble helper factor(s) involved in development of cytotoxic T lymphocytes (CTL). Antigens associated with the Mls locus, I and K/D regions of the MHC were all capable of stimulating responder cells in MLC to produce helper factor. These supernatant fluids were all capable of providing "help" for the generation of cytotoxic T lymphocytes in MLC in which spleen cells are stimulated by allogeneic heat-treated thymocytes or splenocytes. Previous reports from our laboratory as well as others have shown that heat-treated cells do not stimulate a cytotoxic response. Heat-treatment of Mls, I, and H-2K/H-2D region incompatible stimulatory cells in MLC eliminated their ability to induce responder cells to produce helper factor, suggesting this is the mechanism whereby heat-treatment reduces the ability of cells to stimulate cell-mediated lympholysis (CML). The inability of supernatant fluids, from MLCs in which heat-treated cells were the stimulators, to assist in the generation of cytotoxic T cells did not appear to be the result of any suppressive factor induced by such treatment. Further, the antigens that stimulate pre-killer cells appear functionally distinct from those heat labile antigens (Mls, I, H-2K/H-2D associated) that stimulate helper factor production since heat-treated allogeneic cells served as stimulators of cytotoxicity provided helper activity was added to the MLC.

摘要

本研究检测了刺激细胞毒性T淋巴细胞(CTL)发育过程中涉及的可溶性辅助因子产生或释放的抗原。与Mls基因座、主要组织相容性复合体(MHC)的I区和K/D区相关的抗原均能够刺激混合淋巴细胞培养(MLC)中的反应细胞产生辅助因子。这些上清液均能够为MLC中细胞毒性T淋巴细胞的产生提供“帮助”,在MLC中脾细胞由同种异体热处理的胸腺细胞或脾细胞刺激。我们实验室以及其他实验室之前的报告表明,热处理的细胞不会刺激细胞毒性反应。在MLC中对Mls、I区以及H-2K/H-2D区不相容的刺激细胞进行热处理,消除了它们诱导反应细胞产生辅助因子的能力,这表明这就是热处理降低细胞刺激细胞介导的淋巴细胞溶解(CML)能力的机制。来自以热处理细胞作为刺激物的MLC的上清液无法协助细胞毒性T细胞的产生,这似乎不是这种处理诱导的任何抑制因子的结果。此外,刺激前杀伤细胞的抗原在功能上似乎与那些刺激辅助因子产生的热不稳定抗原(与Mls、I区、H-2K/H-2D相关)不同,因为如果向MLC中添加辅助活性,热处理的同种异体细胞可作为细胞毒性的刺激物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验