Graus Y, Meng F, Vincent A, van Breda Vriesman P, de Baets M
Department of Immunology, University of Limburg, Maastricht, The Netherlands.
J Immunol. 1995 Jun 15;154(12):6382-96.
Autoantibodies directed against the acetylcholine receptor (AChR) lead to AChR loss and muscular weakness in myasthenia gravis and its experimental model, experimental autoimmune myasthenia gravis (EAMG). The role of different anti-AChR sequences and specificities in the pathogenesis of EAMG was investigated by sequencing a panel of 19 mouse mAbs, previously elicited against Torpedo and human AChR, that bound to at least four different epitope regions. The pathogenicity of eight mAbs that cross-reacted with mouse or rat AChR was tested. EAMG was induced by four mAbs against the main immunogenic region (MIR). Sequence analysis of different anti-AChR specificities showed a large diversity of H and L chain sequences. Highly homologous H chain sequences (> 90%) were found among some mAbs with similar specificities, whereas highly homologous L chain sequences were not restricted to Abs of a particular fine specificity. Sharing of a highly homologous VH gene or an identical DJH region was observed among three of four pathogenic anti-MIR mAbs, obtained by immunization with AChRs from different species. The VH genes of these three pathogenic mAbs were closely related to PC7183 germline genes indicating that some pathogenic Abs may already be present in the germline repertoire.
针对乙酰胆碱受体(AChR)的自身抗体导致重症肌无力及其实验模型——实验性自身免疫性重症肌无力(EAMG)中AChR丧失和肌肉无力。通过对一组19种小鼠单克隆抗体进行测序,研究了不同抗AChR序列和特异性在EAMG发病机制中的作用,这些单克隆抗体先前是针对电鳐和人AChR产生的,它们与至少四个不同的表位区域结合。测试了八种与小鼠或大鼠AChR发生交叉反应的单克隆抗体的致病性。四种针对主要免疫原性区域(MIR)的单克隆抗体诱导了EAMG。不同抗AChR特异性的序列分析显示重链和轻链序列具有很大的多样性。在一些具有相似特异性的单克隆抗体中发现了高度同源的重链序列(>90%),而高度同源的轻链序列并不局限于具有特定精细特异性的抗体。在用来自不同物种的AChR免疫获得的四种致病性抗MIR单克隆抗体中的三种中,观察到共享高度同源的VH基因或相同的DJH区域。这三种致病性单克隆抗体的VH基因与PC7183种系基因密切相关,表明一些致病性抗体可能已经存在于种系库中。