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葡萄球菌肠毒素激活的脾细胞可被动转移BB/Wor大鼠的糖尿病。

Staphylococcal enterotoxin-activated spleen cells passively transfer diabetes in BB/Wor rat.

作者信息

Ellerman K E, Like A A

机构信息

University of Massachusetts Medical School, Department of Pathology, Worcester 01655.

出版信息

Diabetes. 1992 Apr;41(4):527-32. doi: 10.2337/diab.41.4.527.

Abstract

BB/Wor rats develop spontaneous autoimmune diabetes similar to human insulin-dependent diabetes mellitus. A T-cell-mediated pathogenesis for BB/Wor diabetes is indicated because disease is prevented by neonatal or adult thymectomy and treatment of diabetes-prone rats with monoclonal antibodies directed against CD5 or CD8 T-cell surface markers. Disease can be adoptively transferred with injections of concanavalin A-activated spleen cells from either acutely diabetic or RT6.1 T-cell-depleted diabetes-resistant BB/Wor rats. We used microbial superantigens to stimulate spleen cells from RT6.1 T-cell-depleted diabetes-resistant rats and demonstrated that such cells activated with staphylococcal enterotoxins (SEs) can also transfer diabetes. The diabetogenic effector T cells are readily activated by SEA, SEC3, and SEE, whereas SEB- and SEC2-activated cells are far less effective in the adoptive transfer of diabetes. These results demonstrate that microbial superantigens are capable of activating self-reactive and diabetes-inducing T cells in vitro in the BB/Wor rat. Ubiquitous microorganisms may be the environmental trigger for autoimmunity in susceptible individuals.

摘要

BB/Wor大鼠会发展出与人类胰岛素依赖型糖尿病相似的自发性自身免疫性糖尿病。有迹象表明BB/Wor糖尿病是由T细胞介导的发病机制,因为新生期或成年期胸腺切除以及用针对CD5或CD8 T细胞表面标志物的单克隆抗体治疗糖尿病易患大鼠可预防疾病。通过注射来自急性糖尿病或RT6.1 T细胞耗竭的糖尿病抗性BB/Wor大鼠的伴刀豆球蛋白A激活的脾细胞,疾病可以被过继转移。我们使用微生物超抗原来刺激RT6.1 T细胞耗竭的糖尿病抗性大鼠的脾细胞,并证明用葡萄球菌肠毒素(SEs)激活的此类细胞也能转移糖尿病。致糖尿病效应T细胞很容易被SEA、SEC3和SEE激活,而SEB和SEC2激活的细胞在糖尿病的过继转移中效果要差得多。这些结果表明,微生物超抗原能够在体外激活BB/Wor大鼠的自身反应性和诱导糖尿病的T细胞。普遍存在的微生物可能是易感个体自身免疫的环境触发因素。

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