Jones D R, Thompson R J, Rao S A, Imrie H
Department of Immunology, University Hospital, Queen's Medical Centre, Nottingham, UK.
J Immunol Methods. 1994 Dec 28;177(1-2):235-42. doi: 10.1016/0022-1759(94)90161-9.
We have developed an ELISA technique to examine RBC-bound molecules in autoimmune disorders. In particular, the technique has enabled us to investigate the role of some complement regulatory proteins in immune complex transport and to suggest that decay accelerating factor (DAF) may be involved in this process. In both autoimmune haemolytic anaemia (AHA) and systemic lupus erythematosus (SLE) a sub-set of individuals was identified, on the basis of patterns of complement receptor 1 (CR1) expression on RBC. In these patients, CR1 identified using the monoclonal antibody E11 was low or absent whereas CR1 identified using a DAKO monoclonal antibody (C3RTo5) was present at normal levels.
我们开发了一种酶联免疫吸附测定(ELISA)技术,用于检测自身免疫性疾病中与红细胞(RBC)结合的分子。特别是,该技术使我们能够研究某些补体调节蛋白在免疫复合物运输中的作用,并表明衰变加速因子(DAF)可能参与了这一过程。在自身免疫性溶血性贫血(AHA)和系统性红斑狼疮(SLE)中,根据红细胞上补体受体1(CR1)的表达模式,确定了一部分个体。在这些患者中,使用单克隆抗体E11鉴定的CR1水平较低或缺失,而使用达科(DAKO)单克隆抗体(C3RTo5)鉴定的CR1水平正常。