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实验性自身免疫性肝炎:疾病诱导、病程及T细胞反应性

Experimental autoimmune hepatitis: disease induction, time course and T-cell reactivity.

作者信息

Lohse A W, Manns M, Dienes H P, Meyer zum Büschenfelde K H, Cohen I R

机构信息

Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Hepatology. 1990 Jan;11(1):24-30. doi: 10.1002/hep.1840110106.

Abstract

This study describes a murine model of autoimmune hepatitis: experimental autoimmune hepatitis. Experimental autoimmune hepatitis could be induced most effectively in male C57BL/6 mice by intraperitoneal immunization with the 100,000 g supernatant of syngeneic liver homogenate (S-100) in complete Freund's adjuvant. BALB/C and C3H mice were less susceptible than C57BL/6 mice. Experimental autoimmune hepatitis could not be induced in Lewis rats. Intraperitoneal immunization was more effective than intramuscular or subcutaneous injections, and the amount of protein administered above a threshold was of little influence. A single intraperitoneal injection of S-100 in complete Freund's adjuvant resulted in hepatitis of at least 6 mo duration. Histological changes were most marked 4 wk after disease induction. The histological findings were characterized mainly by perivascular inflammatory infiltrates and hepatocyte necroses. The histological changes were accompanied by biochemical evidence of liver cell death. Passive transfer of experimental autoimmune hepatitis with concanavalin A-activated splenocytes was possible. Specific T-cell reactivity against fractions of S-100 could be demonstrated in vitro. Thus experimental autoimmune hepatitis is a murine model of autoimmune hepatitis probably mediated by autoreactive T cells. It will allow studies of the pathogenesis of autoimmune hepatitis.

摘要

本研究描述了一种自身免疫性肝炎的小鼠模型

实验性自身免疫性肝炎。通过在完全弗氏佐剂中腹腔注射同基因肝匀浆100,000 g上清液(S-100),可在雄性C57BL/6小鼠中最有效地诱导实验性自身免疫性肝炎。BALB/C和C3H小鼠比C57BL/6小鼠更不易感。在Lewis大鼠中无法诱导出实验性自身免疫性肝炎。腹腔注射比肌肉注射或皮下注射更有效,且超过阈值的蛋白给药量影响不大。在完全弗氏佐剂中单次腹腔注射S-100可导致持续至少6个月的肝炎。疾病诱导后4周组织学变化最为明显。组织学表现主要特征为血管周围炎性浸润和肝细胞坏死。这些组织学变化伴有肝细胞死亡的生化证据。用刀豆蛋白A激活的脾细胞被动转移实验性自身免疫性肝炎是可行的。在体外可证明针对S-100各组分的特异性T细胞反应性。因此,实验性自身免疫性肝炎是一种可能由自身反应性T细胞介导的自身免疫性肝炎小鼠模型。它将有助于研究自身免疫性肝炎的发病机制。

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