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通过分析鼠单克隆VIII:C抑制剂中的交叉反应性公共独特型鉴定六种功能性凝血因子VIII:C表位

Identification of six functional clotting factor VIII:C epitopes by analysis of cross-reactive public idiotypes in murine monoclonal VIII:C inhibitors.

作者信息

Tiarks C, Ghalili K, Humphreys R E, Goodall A H, Tuddenham E G, Pechet L

出版信息

Thromb Res. 1987 Mar 1;45(5):527-37. doi: 10.1016/0049-3848(87)90315-x.

Abstract

Six factor VIII:C epitopes which can elicit clotting factor inhibitory antibodies were demonstrated by analysis of public idiotypes of murine monoclonal anti-VIII:C inhibitors. Anti-idiotypic immunoradiometric assays were developed with rabbit antibodies to murine VIII:C inhibitors: Synbiotics, Hybritech, C7F7 and RFF-VIIIC/8. Crossreactions among 10 murine monoclonal antibodies (MoAbs) to VIII:C were tested, showing 6 functional and immunospecific VIII:C epitopes. One epitope on the C-terminal, 80,000 dalton fragment of VIII:C was identified with cross-reaction among 3 MoAbs (Synbiotics, Chemicon, and IB3). Another unique site on this same fragment was recognized with C7F7. Two MoAbs (RFF-VIIIC/6 and RFF-VIIIC/8) defined another site with cross-reactive idiotypes on the N-terminal, 90,000 dalton fragment. Hybritech MoAb identified a fourth functionally distinct site to which no other cross-reacting MoAbs bound. A fifth functional locus was defined with RFF-VIIIC/2 which reacted with an N-terminal site (distinct from the RFF-VIIIC/6 X RFF-VIIIC/8-defined site). A sixth functional locus was recognized with RFF-VIIIC/5 which reacted with a C-terminal site (distinct from the Synbiotics/Chemicon/IB3-defined site but possibly near the C7F7-defined site). RFF-VIIIC/10 identified a non-functional locus on the middle region of VIII:C. These MoAb-based assays resolve six sites to which high-titered inhibitors are directed and offer a path to further study the immunoregulation of human anti-VIII:C inhibitors.

摘要

通过对鼠单克隆抗VIII:C抑制剂的公共独特型进行分析,证实了六种可引发凝血因子抑制性抗体的VIII:C表位。利用兔抗鼠VIII:C抑制剂抗体(Synbiotics、Hybritech、C7F7和RFF-VIIIC/8)开发了抗独特型免疫放射分析。测试了10种针对VIII:C的鼠单克隆抗体(MoAb)之间的交叉反应,显示出6个功能性和免疫特异性的VIII:C表位。在VIII:C的C末端80,000道尔顿片段上的一个表位被3种MoAb(Synbiotics、Chemicon和IB3)交叉反应所识别。在同一片段上的另一个独特位点被C7F7识别。两种MoAb(RFF-VIIIC/6和RFF-VIIIC/8)在N末端90,000道尔顿片段上定义了另一个具有交叉反应独特型的位点。Hybritech MoAb识别出第四个功能上不同的位点,没有其他交叉反应的MoAb与之结合。用RFF-VIIIC/2定义了第五个功能位点,它与一个N末端位点反应(不同于RFF-VIIIC/6×RFF-VIIIC/8定义的位点)。用RFF-VIIIC/5识别出第六个功能位点,它与一个C末端位点反应(不同于Synbiotics/Chemicon/IB3定义的位点,但可能靠近C7F7定义的位点)。RFF-VIIIC/10在VIII:C的中间区域识别出一个非功能位点。这些基于MoAb的分析确定了高滴度抑制剂所针对的六个位点,并为进一步研究人类抗VIII:C抑制剂的免疫调节提供了途径。

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