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超抗原参与胰岛素依赖型糖尿病病因学的证据。

Evidence for superantigen involvement in insulin-dependent diabetes mellitus aetiology.

作者信息

Conrad B, Weidmann E, Trucco G, Rudert W A, Behboo R, Ricordi C, Rodriquez-Rilo H, Finegold D, Trucco M

机构信息

Department of Pediatrics, Rangos Research Center, Children's Hospital of Pittsburgh, Pennsylvania.

出版信息

Nature. 1994 Sep 22;371(6495):351-5. doi: 10.1038/371351a0.

Abstract

Insulin-dependent diabetes mellitus (IDDM) is a T-cell-mediated autoimmune disease whose onset is believed to be triggered by unknown environmental factors acting on a predisposing genetic background. Islet-infiltrating T (IIT) cells from two IDDM patients, who had died at the onset of the disease from brain swelling as a complication of ketoacidosis, were analysed. The results provided evidence for the involvement of a pancreatic islet cell membrane-bound superantigen as a diabetes aetiopathogenetic factor. There was a selective expansion of a T-cell receptor (TCR) variable segment of the beta-chain (V beta 7) in these IIT cells in association with unselected V alpha-chain segments; extensive junctional diversity of the TCR V beta 7 chains; and evidence of positive selection, after exposure to diabetic islet cell membrane preparations, of V beta 7+ T-cell clones among peripheral blood lymphocytes from non-diabetic individuals.

摘要

胰岛素依赖型糖尿病(IDDM)是一种由T细胞介导的自身免疫性疾病,其发病被认为是由作用于易感遗传背景的未知环境因素触发的。对两名IDDM患者的胰岛浸润性T(IIT)细胞进行了分析,这两名患者在疾病发作时因酮症酸中毒并发症脑肿胀而死亡。结果为胰腺胰岛细胞膜结合超抗原作为糖尿病发病机制因素的参与提供了证据。在这些IIT细胞中,β链(Vβ7)的T细胞受体(TCR)可变区有选择性扩增,与未选择的Vα链片段相关;TCR Vβ7链有广泛的连接多样性;并且有证据表明,在接触糖尿病胰岛细胞膜制剂后,非糖尿病个体外周血淋巴细胞中的Vβ7+T细胞克隆发生了阳性选择。

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