Peng S L, Moslehi J, Robert M E, Craft J
Department of Biology, Yale University, New Haven, CT 06510, USA.
J Immunol. 1998 Jan 15;160(2):652-60.
The roles of cytolytic regulatory mechanisms in the immune system of lupus-prone mice were examined in perforin-deficient animals bearing functional or defective (lpr) Fas Ag (CD95). Perforin-deficient Fas+ animals developed accelerated autoimmunity, characterized by increased hypergammaglobulinemia, autoantibody production, and immune deposit-related end-organ disease compared with perforin-intact counterparts. In comparison, perforin-deficient lpr animals had accelerated mortality compared with perforin-intact lpr mice, associated with the abnormal accumulation of CD3+CD4-CD8- alphabeta T cells in conjunction with unaltered hypergammaglobulinemia, autoantibody production, and immune complex renal disease. These results indicate that cytolytic lymphoid regulation plays critical roles in the immune homeostasis of lupus-prone animals, and identify perforin-mediated cytotoxicity as a specific mechanism in the regulation of systemic autoimmunity.
在携带功能性或缺陷性(lpr)Fas抗原(CD95)的穿孔素缺陷动物中,研究了溶细胞调节机制在易患狼疮小鼠免疫系统中的作用。与穿孔素正常的同窝小鼠相比,穿孔素缺陷的Fas+动物出现了加速的自身免疫,其特征为高球蛋白血症增加、自身抗体产生以及与免疫沉积物相关的终末器官疾病。相比之下,与穿孔素正常的lpr小鼠相比,穿孔素缺陷的lpr动物死亡率加速,这与CD + CD4 - CD8 - αβT细胞的异常积累有关,同时伴有高球蛋白血症、自身抗体产生和免疫复合物肾病未改变。这些结果表明,溶细胞性淋巴细胞调节在易患狼疮动物的免疫稳态中起关键作用,并确定穿孔素介导的细胞毒性是调节系统性自身免疫的一种特定机制。