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在易感个体中,甲型肝炎病毒被确认为自身免疫性1型慢性肝炎的触发因素。

Identification of hepatitis A virus as a trigger for autoimmune chronic hepatitis type 1 in susceptible individuals.

作者信息

Vento S, Garofano T, Di Perri G, Dolci L, Concia E, Bassetti D

机构信息

Infectious Diseases Unit, A. Pugliese Hospital, Catanzaro, Italy.

出版信息

Lancet. 1991 May 18;337(8751):1183-7. doi: 10.1016/0140-6736(91)92858-y.

Abstract

To identify factors contributing to the pathogenesis of autoimmune chronic active hepatitis (CAH) healthy relatives of 13 patients with the disorder were followed prospectively for 4 years. 58 relatives were monitored for various serological markers and for T-lymphocyte migration inhibitory activity every 2 months. 3 cases of subclinical acute hepatitis A occurred during the study. In 2 of the 3 subjects, before hepatitis A virus (HAV) infection, there was a defect in suppressor-inducer T lymphocytes specifically controlling immune responses to the asialoglycoprotein receptor, an antigen expressed on the hepatocyte surface. In these 2 subjects, specific helper T cells and antibodies to the asialoglycoprotein receptor persisted and increased after acute hepatitis A, and autoimmune CAH type 1 developed within 5 months. Thus, in susceptible individuals HAV is a trigger for autoimmune CAH.

摘要

为了确定自身免疫性慢性活动性肝炎(CAH)发病机制中的相关因素,对13例该疾病患者的健康亲属进行了为期4年的前瞻性随访。每2个月对58名亲属进行各种血清学标志物和T淋巴细胞迁移抑制活性监测。研究期间发生了3例亚临床甲型肝炎。在这3名受试者中的2名中,甲型肝炎病毒(HAV)感染前,特异性控制对脱唾液酸糖蛋白受体(一种在肝细胞表面表达的抗原)免疫反应的抑制诱导型T淋巴细胞存在缺陷。在这2名受试者中,急性甲型肝炎后,脱唾液酸糖蛋白受体的特异性辅助性T细胞和抗体持续存在并增加,且在5个月内发展为1型自身免疫性CAH。因此,在易感个体中,HAV是自身免疫性CAH的触发因素。

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