Prodeus A P, Goerg S, Shen L M, Pozdnyakova O O, Chu L, Alicot E M, Goodnow C C, Carroll M C
The Center for Blood Research, Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Immunity. 1998 Nov;9(5):721-31. doi: 10.1016/s1074-7613(00)80669-x.
The role of complement in the maintenance of self-tolerance has been examined in two models: an immunoglobulin transgenic model of peripheral tolerance and a lupus-like murine model of CD95 (Fas) deficiency. We find that self-reactive B lymphocytes deficient in complement receptors CD21/CD35 or transferred into mice deficient in the complement protein C4 are not anergized by soluble self-antigen. In the second model, deficiency in CD21/CD35 or C4 combined with CD95 deficiency results in high titers of anti-nuclear antibodies leading to severe lupus-like disease. These findings suggest a novel role for the complement system in B cell tolerance and provide insight into the genetic association of complement deficiency with susceptibility to systemic lupus erythematosus.
一种是外周耐受的免疫球蛋白转基因模型,另一种是CD95(Fas)缺陷的狼疮样小鼠模型。我们发现,缺乏补体受体CD21/CD35的自身反应性B淋巴细胞,或转移到缺乏补体蛋白C4的小鼠体内的自身反应性B淋巴细胞,不会因可溶性自身抗原而失能。在第二种模型中,CD21/CD35或C4的缺陷与CD95的缺陷相结合,会导致高滴度的抗核抗体,进而引发严重的狼疮样疾病。这些发现表明补体系统在B细胞耐受中具有新的作用,并为补体缺陷与系统性红斑狼疮易感性的遗传关联提供了见解。