Mountz J D, Bluethmann H, Zhou T, Wu J
Department of Medicine, University of Alabama at Birmingham 35294.
Semin Immunol. 1994 Feb;6(1):27-37. doi: 10.1006/smim.1994.1005.
Although autoreactive T cells are thought to play a prominent role in autoimmune disease in MRL-lpr/lpr mice, it has been difficult to directly determine if autoreactive T cells escape from the thymus and react with self-antigens in the periphery. To identify a possible defect in clonal deletion or clonal anergy induction of auto-specific T cells, we have studied C57BL/6-lpr/lpr transgenic mouse expressing TCR genes that recognize a known self-antigen, the male H-Y antigen and analyzed clonal deletion and tolerance induction after neonatal tolerance induction with the class II MHC reactive superantigen staphylococcal enterotoxin B (SEB) in V beta 8 TCR transgenic and non-transgenic MRL-lpr/lpr mice. In lpr/lpr mice, the main defect was a thymic-dependent loss of self-tolerance by auto-specific T cells and also a small defect of clonal deletion of autoreactive thymocytes. Defective expression of the Fas apoptosis antigen results from the insertion of the ETn retrotransposon. The fas defect can be partially corrected in TCR-beta TCR transgenic mice in which accelerated T cell development prevents the lymphoproliferative disease and in CD2-fas transgenic mice in which fas expression is corrected in T cells. These results suggest that expression of the TCR-beta, fas and retrovirus genes are co-regulated during early thymocyte development, most likely by common enhancer transcription factors.
尽管自身反应性T细胞被认为在MRL-lpr/lpr小鼠的自身免疫疾病中起重要作用,但一直难以直接确定自身反应性T细胞是否从胸腺逃逸并在外周与自身抗原发生反应。为了确定自身特异性T细胞在克隆清除或克隆无能诱导方面可能存在的缺陷,我们研究了表达识别已知自身抗原——雄性H-Y抗原的TCR基因的C57BL/6-lpr/lpr转基因小鼠,并分析了在Vβ8 TCR转基因和非转基因MRL-lpr/lpr小鼠中用II类MHC反应性超抗原葡萄球菌肠毒素B(SEB)进行新生期耐受诱导后的克隆清除和耐受诱导情况。在lpr/lpr小鼠中,主要缺陷是自身特异性T细胞胸腺依赖性自身耐受的丧失,以及自身反应性胸腺细胞克隆清除的小缺陷。Fas凋亡抗原的缺陷表达是由于ETn逆转座子的插入。在TCR-β TCR转基因小鼠中,加速的T细胞发育可预防淋巴细胞增生性疾病;在CD2-fas转基因小鼠中,T细胞中的fas表达得到纠正,fas缺陷可在一定程度上得到纠正。这些结果表明,TCR-β、fas和逆转录病毒基因的表达在早期胸腺细胞发育过程中共同调节,最有可能是由共同的增强子转录因子调节。