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自身免疫性肾小管间质性肾炎的诱导、特征描述及细胞移植

Induction, characterization, and cell transfer of autoimmune tubulointerstitial nephritis.

作者信息

Bannister K M, Ulich T R, Wilson C B

机构信息

Department of Immunology, Research Institute of Scripps Clinic, La Jolla, California.

出版信息

Kidney Int. 1987 Nov;32(5):642-51. doi: 10.1038/ki.1987.256.

Abstract

Autoimmune tubulointerstitial nephritis (TIN) was induced in Lewis (LEW) rats by immunization with homologous Brown-Norway (BN) rat renal basement membrane (RBM), complete Freund's adjuvant and Bordetella pertussis vaccine. The BN strain has a tubular basement membrane (TBM) antigen (Ag+) detectable by immunofluorescence which is lacking in unmodified LEW rat TBM. Development of TIN in LEW rats correlated with TBM Ag+ immunogens from homologous and heterologous RBM preparations. By day 14 after immunization TIN developed characterized by elevated serum creatinine levels and by tubular destruction with focal, circumscribed lesions containing epithelioid cells, giant cells and mononuclear cell infiltrates. Approximately 60% of the mononuclear cells bore T cell antigens with most cells expressing Ia markers. Immunofluorescence and elution studies revealed no selective IgG fixation to TBM at day 14 despite high titers of circulating alloantibody reactive with the immunizing TBM. Intravenous transfer of LNC and/or splenic cells (3.5 to 7 X 10(8)) to naive LEW rats resulted in less severe but histologically identical TIN in seven days with T cell subpopulations similar to those seen in the active model. This model strongly suggests an initiating role for cell-mediated immunity in TIN in the rat and may provide a parallel to human TIN.

摘要

通过用同源的布朗-挪威(BN)大鼠肾基底膜(RBM)、完全弗氏佐剂和百日咳疫苗免疫,在刘易斯(LEW)大鼠中诱导出自身免疫性肾小管间质性肾炎(TIN)。BN品系具有可通过免疫荧光检测到的肾小管基底膜(TBM)抗原(Ag+),而未修饰的LEW大鼠TBM中缺乏该抗原。LEW大鼠中TIN的发展与来自同源和异源RBM制剂的TBM Ag+免疫原相关。免疫后第14天,TIN出现,其特征为血清肌酐水平升高以及肾小管破坏,伴有含有上皮样细胞、巨细胞和单核细胞浸润的局灶性、局限性病变。大约60%的单核细胞带有T细胞抗原,大多数细胞表达Ia标志物。免疫荧光和洗脱研究显示,尽管循环中与免疫TBM反应的同种抗体滴度很高,但在第14天时没有选择性IgG固定到TBM上。将淋巴细胞(LNC)和/或脾细胞(3.5至7×10⁸)静脉注射到未免疫的LEW大鼠中,7天后导致较轻但组织学上相同的TIN,其T细胞亚群与在活性模型中所见相似。该模型强烈提示细胞介导的免疫在大鼠TIN中起启动作用,并且可能与人类TIN有相似之处。

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