Wu D P, Gilkeson G S, Armitage J, Reich C F, Pisetsky D S
Medical Research Service, Durham VA Hospital, NC 27705.
Clin Exp Immunol. 1990 Oct;82(1):33-7.
To assess the immune recognition of DNA in systemic lupus erythematosus, the antigenic specificity of monoclonal anti-DNA antibodies from autoimmune MRL-lpr/lpr mice was investigated Determinant specificity was assessed by ELISA in terms of binding to a panel of ssDNA antigens including calf thymus, human placenta, Escherichia coli, Clostridium perfringens, Micrococcus lysodeikticus, salmon testes, chicken blood and murine DNA. Among the monoclonal antibodies, a variety of binding patterns was observed, although for all antibodies tested murine DNA was among the most reactive antigens. Binding to other DNAs varied markedly, with some antibodies showing only low reactivity to certain antigens in the test panel. Similar results were obtained with sera of individual MRL-lpr/lpr mice. These results suggest that anti-DNA antibodies bind specific antigenic determinants variably expressed by DNAs of various species. Furthermore, the preferential binding to mouse DNA by some MRL-lpr/lpr antibodies may suggest a role of self-DNA in the in vivo selection of anti-DNA antibodies for expression.
为评估系统性红斑狼疮中DNA的免疫识别情况,研究了自身免疫性MRL-lpr/lpr小鼠单克隆抗DNA抗体的抗原特异性。通过酶联免疫吸附测定(ELISA),根据与一组单链DNA抗原(包括小牛胸腺、人胎盘、大肠杆菌、产气荚膜梭菌、溶壁微球菌、鲑鱼睾丸、鸡血和鼠DNA)的结合情况来评估决定簇特异性。在这些单克隆抗体中,观察到了多种结合模式,尽管对于所有测试抗体而言,鼠DNA都是反应性最强的抗原之一。与其他DNA的结合差异显著,一些抗体对测试组中的某些抗原仅表现出低反应性。对个体MRL-lpr/lpr小鼠血清也获得了类似结果。这些结果表明,抗DNA抗体结合不同物种DNA可变表达的特定抗原决定簇。此外,一些MRL-lpr/lpr抗体对小鼠DNA的优先结合可能表明自身DNA在体内选择表达抗DNA抗体中起作用。