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人类细胞毒性T淋巴细胞相关抗原4(CTLA-4)原位表达于生发中心的T淋巴细胞、皮肤移植物抗宿主病以及霍奇金病中。

Human CTLA-4 is expressed in situ on T lymphocytes in germinal centers, in cutaneous graft-versus-host disease, and in Hodgkin's disease.

作者信息

Vandenborre K, Delabie J, Boogaerts M A, De Vos R, Lorré K, De Wolf-Peeters C, Vandenberghe P

机构信息

Laboratory for Experimental Hematology, University of Leuven, Belgium.

出版信息

Am J Pathol. 1998 Apr;152(4):963-73.

Abstract

Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4, CD152) is a molecule expressed on in vitro activated T cells. CTLA-4 shares important sequence homology with CD28 and binds to the same ligands, CD80 (B7-1) and CD86 (B7-2). CTLA-4 probably functions as a negative regulator of T lymphocyte activation in the mouse, although this remains to be proven for human T lymphocytes. We have developed new monoclonal antibodies against human CTLA-4 and have investigated the in situ expression of CTLA-4 in a wide variety of normal and pathological human tissues expressing CD80 and CD86. As revealed in this study, CTLA-4 is expressed on thymocytes in thymic medulla, on a subset of CD4+ T lymphocytes in germinal centers of follicular hyperplasia, on T cells, mainly CD8+, infiltrating skin affected by graft-versus-host disease, and on T cells, mainly CD4+, infiltrating Hodgkin's disease lesions. In immunoelectron microscopy, CTLA-4 was found on the plasma membrane as well as in the hyaloplasm and cytoplasmic vesicles, in agreement with its pattern of expression on in vitro activated T cells. Interestingly, no or at most scarce expression of CTLA-4 was found in granulomatous lymph nodes, T-cell-mediated inflammatory diseases, or non-Hodgkin's lymphomas, regardless of their expression of CD80 or CD86. Thus, expression of CTLA-4 appears to be induced in selective pathological conditions in vivo. The pathways leading to selective induction of CTLA-4 and its role in the pathophysiology of these conditions need to be further investigated.

摘要

细胞毒性T淋巴细胞相关抗原4(CTLA-4,CD152)是一种在体外活化的T细胞上表达的分子。CTLA-4与CD28具有重要的序列同源性,并与相同的配体CD80(B7-1)和CD86(B7-2)结合。在小鼠中,CTLA-4可能作为T淋巴细胞活化的负调节因子发挥作用,尽管这一点在人类T淋巴细胞中仍有待证实。我们已开发出针对人类CTLA-4的新型单克隆抗体,并研究了CTLA-4在多种表达CD80和CD86的正常和病理人类组织中的原位表达。如本研究所示,CTLA-4在胸腺髓质的胸腺细胞上表达,在滤泡增生生发中心的一部分CD4+T淋巴细胞上表达,在受移植物抗宿主病影响的浸润皮肤的T细胞(主要是CD8+)上表达,以及在浸润霍奇金病病变的T细胞(主要是CD4+)上表达。在免疫电子显微镜下,CTLA-4在质膜以及透明质和细胞质小泡中被发现,这与其在体外活化T细胞上的表达模式一致。有趣的是,在肉芽肿性淋巴结、T细胞介导的炎症性疾病或非霍奇金淋巴瘤中,无论它们是否表达CD80或CD86,均未发现或至多仅发现CTLA-4的少量表达。因此,CTLA-4的表达似乎是在体内选择性病理条件下被诱导的。导致CTLA-4选择性诱导的途径及其在这些疾病病理生理学中的作用有待进一步研究。

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