首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Human CTLA-4 is expressed in situ on T lymphocytes in germinal centers in cutaneous graft-versus-host disease and in Hodgkins disease.
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Human CTLA-4 is expressed in situ on T lymphocytes in germinal centers in cutaneous graft-versus-host disease and in Hodgkins disease.

机译:人CTLA-4在生发中心皮肤移植物抗宿主病和霍奇金氏病中的T淋巴细胞上原位表达。

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摘要

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.
机译:细胞毒性T淋巴细胞相关抗原4(CTLA-4,CD152)是在体外活化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。 CTLA-4可能在小鼠中充当T淋巴细胞活化的负调节剂,尽管对于人类T淋巴细胞仍有待证明。我们已经开发了针对人类CTLA-4的新型单克隆抗体,并研究了CTLA-4在表达CD80和CD86的多种正常和病理性人体组织中的原位表达。正如这项研究所揭示的,CTLA-4在胸腺髓质的胸腺细胞,滤泡增生的生发中心的CD4 + T淋巴细胞的一部分,在T细胞(主要是CD8 +)上浸润受移植物抗宿主病影响的皮肤,以及T细胞,主要是CD4 +,会浸润霍奇金病病变。在免疫电子显微镜中,CTLA-4被发现在质膜​​以及透明质和细胞质囊泡中,与其在体外活化T细胞上的表达方式一致。有趣的是,在肉芽肿性淋巴结,T细胞介导的炎性疾病或非霍奇金淋巴瘤中,无论CD80或CD86的表达如何,都没有或仅有很少的CTLA-4表达。因此,在体内选择性病理条件下似乎诱导了CTLA-4的表达。导致CTLA-4选择性诱导的途径及其在这些疾病的病理生理中的作用有待进一步研究。

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