Whalen B J, Rossini A A, Mordes J P, Greiner D L
Department of Medicine, University of Massachusetts Medical School, Worcester, USA.
Diabetes. 1995 Aug;44(8):963-7. doi: 10.2337/diab.44.8.963.
We have induced autoimmune insulin-dependent diabetes mellitus (IDDM) in athymic WAG rats by transfusing thymocytes from histocompatible phenotypically normal rats of the DR-BB strain. DR-BB rats rarely develop spontaneous IDDM, but readily become hyperglycemic if depleted in vivo of regulatory T-cells that express the RT6.1 maturational alloantigen. Successful adoptive transfer of IDDM by DR-BB thymocytes required that the athymic recipients be depleted of emerging populations of donor-origin RT6.1+ T-cells. Thymocytes from both normal and RT6-depleted diabetic DR donors were equally capable of transferring autoimmunity. In contrast, thymocytes from normal histocompatible YOS rats failed to transfer IDDM. The autoreactive potential of DR-BB rat thymocytes was minimal from birth to 4 weeks of age and then increased substantially at 8-9 weeks of age. These results demonstrate that the DR-BB rat thymus harbors abnormal cell populations predisposed to autoreactivity. The data localize the developmental defect leading to diabetes in the BB rat to an abnormal intrathymic selection process.
我们通过输注来自组织相容性表型正常的DR - BB品系大鼠的胸腺细胞,在无胸腺的WAG大鼠中诱导出自身免疫性胰岛素依赖型糖尿病(IDDM)。DR - BB大鼠很少自发发生IDDM,但如果体内表达RT6.1成熟同种异体抗原的调节性T细胞耗竭,它们很容易出现高血糖。DR - BB胸腺细胞成功过继转移IDDM要求无胸腺受体中供体来源的RT6.1 + T细胞新出现的群体被耗竭。来自正常和RT6缺失的糖尿病DR供体的胸腺细胞转移自身免疫的能力相同。相比之下,来自组织相容性正常的YOS大鼠的胸腺细胞不能转移IDDM。DR - BB大鼠胸腺细胞的自身反应性潜能在出生至4周龄时最小,然后在8 - 9周龄时大幅增加。这些结果表明,DR - BB大鼠胸腺中存在易于发生自身反应性的异常细胞群体。数据将导致BB大鼠糖尿病的发育缺陷定位到异常的胸腺内选择过程。