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胸腺细胞阳性选择的破坏会导致自身免疫。

Disruption of positive selection of thymocytes causes autoimmunity.

作者信息

Kretz-Rommel A, Rubin R L

机构信息

W.M. Keck Autoimmune Disease Center, Department of Molecular and Experimental Medicine, The Scripps Research Institute, MEM 131, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

Nat Med. 2000 Mar;6(3):298-305. doi: 10.1038/73152.

Abstract

To differentiate into T cells, immature thymocytes must engage, through their antigen-specific T-cell receptor, peptides derived from self proteins presented by cortical epithelial cells in the thymus, a process called positive selection. Despite this requirement for self-recognition during development, mature T cells do not normally show autoreactivity. Mice injected in the thymus with procainamide-hydroxylamine, a metabolite of procainamide, develop autoimmune features resembling drug-induced lupus. Here, we show that when thymocytes undergo positive selection in the presence of procainamide-hydroxylamine, they fail to establish unresponsiveness to low affinity selecting self antigens, resulting in systemic autoimmunity.

摘要

为了分化为T细胞,未成熟的胸腺细胞必须通过其抗原特异性T细胞受体,与胸腺中皮质上皮细胞呈递的源自自身蛋白质的肽相互作用,这一过程称为阳性选择。尽管在发育过程中需要这种自我识别,但成熟的T细胞通常不会表现出自反应性。向胸腺中注射普鲁卡因酰胺的代谢产物普鲁卡因酰胺羟胺的小鼠会出现类似药物性狼疮的自身免疫特征。在这里,我们表明,当胸腺细胞在普鲁卡因酰胺羟胺存在的情况下进行阳性选择时,它们无法对低亲和力的选择自身抗原建立无反应性,从而导致全身性自身免疫。

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