Dua H S, Abrams M, Barrett J A, Gregerson D S, Forrester J V, Donoso L A
Research Division, Wills Eye Hospital, Philadelphia.
Curr Eye Res. 1992;11 Suppl:59-65. doi: 10.3109/02713689208999512.
Retinal S-antigen (SAg) and interphotoreceptor retinol-binding protein (IRBP) induced experimental autoimmune uveitis (EAU) and experimental autoimmune pinealitis (EAP) are good models for studying the mechanisms involved in autoimmune diseases. Many immunogenetically active epitopes have been identified in these proteins but immunodominance of one or more epitopes in vivo, has not yet been established. In this paper we present and discuss some experiments that led to the discovery of a dominant "tolerogenic" epitope in SAg. We also demonstrate the presence of cross reactive epitopes in the two potent retinal antigens, SAg and IRBP and finally introduce early data on a unique anti S2.4.c5 idiotypic (Id) monoclonal antibody (MAb) which appears to be a site non associated antibody that binds not only to s2.4.c5 but also to SAg.
视网膜S抗原(SAg)和光感受器间视黄醇结合蛋白(IRBP)诱导的实验性自身免疫性葡萄膜炎(EAU)和实验性自身免疫性松果体炎(EAP)是研究自身免疫性疾病发病机制的良好模型。在这些蛋白质中已鉴定出许多具有免疫遗传活性的表位,但体内一个或多个表位的免疫显性尚未确定。在本文中,我们展示并讨论了一些实验,这些实验导致在SAg中发现了一个显性的“耐受性”表位。我们还证明了两种强效视网膜抗原SAg和IRBP中存在交叉反应性表位,最后介绍了一种独特的抗S2.4.c5独特型(Id)单克隆抗体(MAb)的早期数据,该抗体似乎是一种不与位点相关的抗体,不仅能与s2.4.c5结合,还能与SAg结合。