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CD27-CD27配体/CD70相互作用增强了同种抗原诱导的CD8+T淋巴细胞增殖和细胞溶解活性。

CD27-CD27 ligand/CD70 interactions enhance alloantigen-induced proliferation and cytolytic activity in CD8+ T lymphocytes.

作者信息

Brown G R, Meek K, Nishioka Y, Thiele D L

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center at Dallas 75235, USA.

出版信息

J Immunol. 1995 Apr 15;154(8):3686-95.

PMID:7706711
Abstract

To study the role of CD27-CD27 ligand (CD27L)/CD70 interactions in the generation of murine allospecific T cell responses, SF9 cells or cell membranes expressing recombinant human CD70 were added to in vitro MLC containing C57BL/6 (H-2b) responder cells and class I and II MHC disparate H-2b/d stimulator cells. Alloantigen-specific CTL generation, CD8+ T cell proliferation, and levels of N-alpha-benzyloxycarbonyl-L-lysine thiobenzyl esterase activity were enhanced in the presence of human CD27L/CD70 expressed on SF9 cell membranes. Enhancement of CD8+ T cell responses occurred in the absence of any discernible effects on CD4+ T cell proliferation or IL-2 responses. Additional studies demonstrated that CD27L/CD70-expressing membranes enhanced proliferative responses to class I MHC differences but had no effect on proliferative responses to class II MHC disparities. Enhancement of allospecific CTL generation was also observed when CD27L/CD70-expressing membranes were added only during the last 24 to 48 h of 5-day MLC. Thus, the present studies suggest that CD27-CD27L/CD70 interactions can selectively enhance differentiation of Ag-specific CD8+ T cell effector mechanisms under conditions in which Th cell responses are not altered.

摘要

为研究CD27-CD27配体(CD27L)/CD70相互作用在小鼠同种特异性T细胞应答产生中的作用,将表达重组人CD70的SF9细胞或细胞膜加入到含有C57BL/6(H-2b)应答细胞以及I类和II类主要组织相容性复合体(MHC)不同的H-2b/d刺激细胞的体外混合淋巴细胞培养(MLC)中。在SF9细胞膜上表达的人CD27L/CD70存在的情况下,同种抗原特异性细胞毒性T淋巴细胞(CTL)的产生、CD8+ T细胞增殖以及N-α-苄氧羰基-L-赖氨酸硫代苄酯酶活性水平均得到增强。CD8+ T细胞应答的增强发生在对CD4+ T细胞增殖或白细胞介素-2(IL-2)应答没有任何明显影响的情况下。进一步的研究表明,表达CD27L/CD70的细胞膜增强了对I类MHC差异的增殖反应,但对II类MHC差异的增殖反应没有影响。当仅在5天MLC的最后24至48小时添加表达CD27L/CD70的细胞膜时,也观察到同种特异性CTL产生的增强。因此,本研究表明,在Th细胞应答未改变的条件下,CD27-CD27L/CD70相互作用可选择性增强抗原特异性CD8+ T细胞效应机制的分化。

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