Frauwirth K A, Alegre M L, Thompson C B
Abramson Family Cancer Research Institute and Department of Cancer Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
J Immunol. 2000 Mar 15;164(6):2987-93. doi: 10.4049/jimmunol.164.6.2987.
Immunologic tolerance in T lymphocytes is maintained through both thymic and peripheral contributions. One peripheral tolerance mechanism is the induction of T cell anergy, a form of nonresponsiveness resulting from incomplete T cell activation, such as stimulation through the TCR in the absence of costimulation. Recent reports have suggested that engagement of the inhibitory receptor CTLA-4 by its B7 ligand is critical for the initiation of anergy. We tested the importance of CTLA-4 in anergy induction in primary T cells with an in vitro anergy system. Using both CTLA-4/B7-blocking agents and CTLA-4-deficient T cells, we found that T cell anergy can be established in the absence of CTLA-4 expression and/or function. Even in the absence of CTLA-4 signal transduction, T cells activated solely through TCR ligation lose the ability to proliferate as a result of autocrine IL-2 production upon subsequent receptor engagement. Thus, CTLA-4 signaling is not required for the development of T cell anergy.
T淋巴细胞中的免疫耐受通过胸腺和外周机制共同维持。一种外周耐受机制是诱导T细胞无能,这是一种由于T细胞不完全激活导致的无反应状态,例如在缺乏共刺激的情况下通过TCR刺激。最近的报道表明,抑制性受体CTLA-4与其B7配体的结合对于无能的起始至关重要。我们使用体外无能系统测试了CTLA-4在原代T细胞无能诱导中的重要性。使用CTLA-4/B7阻断剂和CTLA-4缺陷型T细胞,我们发现T细胞无能可以在没有CTLA-4表达和/或功能的情况下建立。即使在没有CTLA-4信号转导的情况下,仅通过TCR连接激活的T细胞由于后续受体结合时自分泌IL-2的产生而失去增殖能力。因此,CTLA-4信号传导对于T细胞无能的发展不是必需的。