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源自自身免疫性MRL/Mp-lpr/lpr小鼠的单克隆抗体诱导狼疮细胞形成。

Lupus erythematosus cell formation by a monoclonal antibody derived from an autoimmune MRL/Mp-lpr/lpr mouse.

作者信息

Kanai Y, Yamauchi S, Hashiba-Kanai Y

机构信息

Department of Molecular Oncology, University of Tokyo, Japan.

出版信息

Immunol Lett. 1989 Jan 15;20(1):9-13. doi: 10.1016/0165-2478(89)90061-8.

Abstract

An MRP-2 monoclonal antibody (MoAb) was primarily a product of hybridoma selected by binding to poly(ADP-ribose) from a lupus prone MRL/Mp-lpr/lpr (MRL/l) mouse, and was shown to cross-react with single-stranded (ss) DNA. Detailed examination revealed that MRP-2 MoAb bound to a conformational epitope formed between double-stranded (ds) DNA and total histone: both H3 and H4 were essential for the formation of this conformational epitope with dsDNA. Because of this characteristic of the MoAb, its ability to induce lupus erythematosus (LE) cells was examined in an indirect LE test with peripheral blood of MRL/Mp-+/+ (MRL/n) mice, which develop a mild form of lupus after the age of one year. MRP-2 MoAb was found to induce hematoxylin bodies, LE rosettes and LE cells, but a direct LE test using MRL/n mouse blood did not induce LE cell phenomena. This is the first demonstration of induction of LE cells by a MoAb that binds to dsDNA-histone complexes.

摘要

一种MRP - 2单克隆抗体(MoAb)最初是通过与来自狼疮易感MRL/Mp - lpr/lpr(MRL/l)小鼠的聚(ADP - 核糖)结合而筛选出的杂交瘤产物,并且已证明其与单链(ss)DNA发生交叉反应。详细检查发现,MRP - 2 MoAb与双链(ds)DNA和总组蛋白之间形成的构象表位结合:H3和H4对于与dsDNA形成这种构象表位都是必不可少的。由于该单克隆抗体的这一特性,在间接LE试验中,使用一岁后会出现轻度狼疮形式的MRL/Mp - +/+(MRL/n)小鼠的外周血来检测其诱导红斑狼疮(LE)细胞的能力。发现MRP - 2 MoAb可诱导苏木精小体、LE花环和LE细胞,但使用MRL/n小鼠血液进行的直接LE试验未诱导出LE细胞现象。这是首次证明与dsDNA - 组蛋白复合物结合的单克隆抗体可诱导LE细胞。

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