Suppr超能文献

用单克隆抗独特型抗体抑制胶原诱导的关节炎。

Collagen-induced arthritis suppressed with monoclonal anti-idiotypic antibody.

作者信息

Tarutani S

机构信息

Department of Biochemistry, Faculty of Dentistry, Kyushu University, Fukuoka, Japan.

出版信息

Microbiol Immunol. 1993;37(2):135-42. doi: 10.1111/j.1348-0421.1993.tb03190.x.

Abstract

In foregoing work, we identified at least 5 distinct epitopes on human type II collagen (CII), using 8 murine monoclonal antibodies (mAb) against human CII, and suggested that a species-nonspecific epitope on CII recognized by anti-CII mAb termed 1-5 is an arthritogenic epitope. We also found that antibody response against a selected epitope of human CII could be induced by immunization with rabbit anti-idiotypic (Id) antibody against anti-CII mAb. The author developed and characterized monoclonal anti-Id antibodies against 1-5 mAb recognizing a putative arthritogenic epitope. The author also investigated whether the anti-Id mAb could regulate antibody response directed against a selected epitope recognized by 1-5 mAb, and the induction of collagen-induced arthritis in DBA/1J mice. DBA/1J mice intravenously preinjected with anti-Id mAb to 1-5, did not produce anti-CII antibody expressing 1-5 Id upon immunization with human CII. Furthermore, as the development of collagen-induced arthritis (CIA) in DBA/1J mice pretreated with anti-Id mAb to 1-5 was significantly suppressed, anti-Id mAb will be a useful tool for studying the regulation of antibody response to a selected epitope. This study lends support to our hypothesis that the 1-5 epitope is an arthritogenic epitope.

摘要

在之前的工作中,我们使用8种针对人II型胶原蛋白(CII)的鼠单克隆抗体(mAb),鉴定出了人CII上至少5个不同的表位,并提出抗CII mAb识别的CII上的一个种属非特异性表位(称为1-5)是一个致关节炎表位。我们还发现,用针对抗CII mAb的兔抗独特型(Id)抗体免疫可诱导针对人CII选定表位的抗体反应。作者制备并鉴定了针对识别假定致关节炎表位的1-5 mAb的单克隆抗Id抗体。作者还研究了抗Id mAb是否能调节针对1-5 mAb识别的选定表位的抗体反应,以及在DBA/1J小鼠中诱导胶原诱导的关节炎。预先静脉注射针对1-5的抗Id mAb的DBA/1J小鼠,在用人CII免疫后未产生表达1-5 Id的抗CII抗体。此外,由于预先用针对1-5的抗Id mAb处理的DBA/1J小鼠中胶原诱导的关节炎(CIA)的发展受到显著抑制,抗Id mAb将成为研究针对选定表位的抗体反应调节的有用工具。本研究支持了我们的假设,即1-5表位是一个致关节炎表位。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验