Bailey N C, Bona A, Dikman S, Bonilla F, Alt F W, Bona C
Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029.
Eur J Immunol. 1991 Apr;21(4):959-65. doi: 10.1002/eji.1830210415.
The NZB mouse is genetically predisposed to the development of autoimmune disease that resembles the human autoimmune systemic lupus erythematosus and autoimmune hemolytic anemia, with increased titers of anti-DNA, and Coombs' autoantibodies. The various autoimmune traits are controlled separately by a limited number of genes. Genetic studies have shown that several immune loci are involved in autoimmunity: T cell abnormalities, H-2 complex and immunoglobulin genes have been implicated. In this report, we present evidence for a significant correlation of NZB V kappa 1 haplotype defined by restriction fragment length polymorphism analysis with anti-erythrocyte autoantibodies in NZB x 129/J and NZB x SM/J recombinant inbred lines.
NZB小鼠在基因上易患自身免疫性疾病,该疾病类似于人类自身免疫性系统性红斑狼疮和自身免疫性溶血性贫血,伴有抗DNA和库姆斯自身抗体滴度升高。各种自身免疫特征由有限数量的基因分别控制。遗传学研究表明,几个免疫基因座与自身免疫有关:T细胞异常、H-2复合体和免疫球蛋白基因都与之相关。在本报告中,我们提供证据表明,通过限制性片段长度多态性分析定义的NZB V κ1单倍型与NZB×129/J和NZB×SM/J重组近交系中的抗红细胞自身抗体存在显著相关性。