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兔实验性慢性活动性肝炎发病机制的研究。I. 疾病的诱导及同种异体肝脏特异性蛋白的保护作用。

Studies on the pathogenesis of experimental chronic active hepatitis in rabbits. I. Induction of the disease and protective effect of allogeneic liver specific proteins.

作者信息

Meyer zum Büschenfelde K H, Hopf U

出版信息

Br J Exp Pathol. 1974 Oct;55(5):498-508.

Abstract

By long-term immunization intraperitoneally over 143 weeks with human liver specific proteins (HLP) together with complete Freund's adjuvant a chronic active hepatitis (CAH) was produced in rabbits, and the protective effect of allogeneic liver specific proteins (RLP) against the development of liver lesions was tested. The animals (white New Zealands) were divided into 6 groups. Immunization with HLP caused in all animals the development of CAH or liver cirrhosis, depending on the antigen dose. An autoimmunity against liver antigens, induced by HLP, persisted by immunization with RLP. The combined application of HLP and RLP (native and aggregate free, respectively) caused the development of histologically demonstrable liver lesions in only 13% of the animals. Underlying the pathogenesis of the experimental CAH is, according to the existing results, a cellular cytotoxicity. This concept is supported by the protective effect of RLP on cellular immune reactions against RLP and the induction of liver lesions. The importance of an antibody mediated cellular cytotoxicity for the pathogenesis of the experimental CAH has to be clarified by further experiments.

摘要

通过在143周内腹腔注射人肝脏特异性蛋白(HLP)并联合完全弗氏佐剂,在兔身上诱导出慢性活动性肝炎(CAH),并测试了同种异体肝脏特异性蛋白(RLP)对肝脏病变发展的保护作用。将动物(白色新西兰兔)分为6组。根据抗原剂量不同,用HLP免疫会使所有动物出现CAH或肝硬化。由HLP诱导的针对肝脏抗原的自身免疫,通过用RLP免疫得以持续。HLP和RLP(分别为天然的和无聚集物的)联合应用仅使13%的动物出现组织学上可证实的肝脏病变。根据现有结果,实验性CAH发病机制的基础是细胞毒性。RLP对针对RLP的细胞免疫反应及肝脏病变诱导的保护作用支持了这一概念。抗体介导的细胞毒性在实验性CAH发病机制中的重要性有待进一步实验阐明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5430/2072675/47137dfe7112/brjexppathol00407-0087-a.jpg

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