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由于自身特异性受体的低水平表达,T细胞受体α基因的等位基因包含会带来自身免疫风险。

Allelic inclusion of T cell receptor alpha genes poses an autoimmune hazard due to low-level expression of autospecific receptors.

作者信息

Sarukhan A, Garcia C, Lanoue A, von Boehmer H

机构信息

Institut Necker, INSERM 373, Paris, France.

出版信息

Immunity. 1998 May;8(5):563-70. doi: 10.1016/s1074-7613(00)80561-0.

Abstract

Organ-specific autoimmune disease can be caused by alphabeta T cells that have escaped self-tolerance induction. Here we show that one of the causes of escape from self-tolerance is the coexpression of two different T cell receptors by the same cell, which can occur in up to 30% of all T cells in normal mice and can lead to low-level surface expression of an autospecific TCR. We found that double receptor-expressing T cells can escape tolerance even to ubiquitously expressed antigens but can nevertheless induce autoimmune diabetes when the relevant protein is expressed in pancreatic tissue. Such diabetogenic T cells are absent, however, among T cells expressing the autospecific TCR as the sole receptor.

摘要

器官特异性自身免疫性疾病可能由逃避自身耐受诱导的αβ T细胞引起。我们在此表明,逃避自身耐受的原因之一是同一细胞共表达两种不同的T细胞受体,这种情况在正常小鼠所有T细胞中发生率可达30%,并可导致自身特异性TCR的低水平表面表达。我们发现,表达双受体的T细胞即使对普遍表达的抗原也能逃避耐受,但当相关蛋白在胰腺组织中表达时,仍可诱导自身免疫性糖尿病。然而,在仅表达自身特异性TCR作为唯一受体的T细胞中,不存在这种致糖尿病的T细胞。

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