Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Nat Immunol. 2010 Feb;11(2):129-35. doi: 10.1038/ni.1835. Epub 2009 Dec 27.
The inhibitory immunoregulatory receptor CTLA-4 is critical in maintaining self-tolerance, but the mechanisms of its actions have remained controversial. Here we examined the antigen specificity of tissue-infiltrating CD4(+) T cells in Ctla4(-/-) mice. After adoptive transfer, T cells isolated from tissues of Ctla4(-/-) mice showed T cell antigen receptor (TCR)-dependent accumulation in the tissues from which they were derived, which suggested reactivity to tissue-specific antigens. We identified the pancreas-specific enzyme PDIA2 as an autoantigen in Ctla4(-/-) mice. CTLA-4 expressed either on PDIA2-specific effector cells or on regulatory T cells was sufficient to control tissue destruction mediated by PDIA2-specific T cells. Our results demonstrate that both cell-intrinsic and non-cell-autonomous actions of CTLA-4 operate to maintain T cell tolerance to a self antigen.
抑制性免疫调节受体 CTLA-4 对于维持自身耐受至关重要,但它的作用机制一直存在争议。在这里,我们研究了 Ctla4(-/-) 小鼠组织浸润的 CD4(+) T 细胞的抗原特异性。在过继转移后,从 Ctla4(-/-) 小鼠组织中分离出的 T 细胞显示出 TCR 依赖性在其来源组织中的积累,这表明对组织特异性抗原的反应性。我们鉴定出胰腺特异性酶 PDIA2 是 Ctla4(-/-) 小鼠中的自身抗原。在 PDIA2 特异性效应细胞上或在调节性 T 细胞上表达的 CTLA-4 足以控制 PDIA2 特异性 T 细胞介导的组织破坏。我们的结果表明,CTLA-4 的细胞内在和非细胞自主作用都可维持对自身抗原的 T 细胞耐受。