Oluwole S F, Chowdhury N C, Jin M X
Department of Surgery, College of Physicians and Surgeons of Columbia University, New York, New York 10032.
Cell Immunol. 1994 Jan;153(1):163-70. doi: 10.1006/cimm.1994.1014.
We have recently demonstrated that intrathymic (IT) inoculation of ultraviolet-B irradiation-modified donor spleen cells induces specific tolerance to organ allografts in transiently immunosuppressed adult rats. This study examines the splenic leukocyte component that plays a role in the induction of organ-specific tolerance when injected into the thymus of an adult animal. Our results showed that in the low responder combination of Lewis-to-ACI, IT inoculation of resting Lewis T-cells consistently induced specific unresponsiveness to cardiac allografts in sublethally irradiated (200 rad total body irradiation) ACI recipients while the same was true in the high responder rat combination of WF-to-Lewis, where recipient rats were transiently immunomodulated with antilymphocyte serum. In contrast, IT inoculation of donor B cells, macrophages, or dendritic cells in similarly prepared animals failed to prolong graft survival in both the low responder (Lewis-to ACI) and the high responder (WF-to-Lewis) rat strain combinations. This observation suggests that donor-specific unresponsiveness can be readily achieved by IT inoculation of major histocompatibility (MHC) class I expressing donor-type resting T-cells rather than by any donor-type antigen presenting cells that express MHC class I and II molecules. Extrathymic inoculation of T-cells in transiently immunosuppressed recipients failed to prevent graft rejection, thus demonstrating the privileged position of the thymus in the induction of tolerance. The unresponsive recipients of cardiac allografts specifically and permanently accepted donor-type second-set islet allografts, thus confirming antigen-specific tolerance in this model. These results suggest that manipulation of the immune system through thymic reeducation of the developing T-cells by the deliberate introduction of foreign MHC class I cellular alloantigens has therapeutic potential in the induction of transplantation tolerance in adult animals.
我们最近证明,在短暂免疫抑制的成年大鼠中,胸腺内(IT)接种经紫外线B照射修饰的供体脾细胞可诱导对器官同种异体移植的特异性耐受。本研究检测了将其注入成年动物胸腺时,在诱导器官特异性耐受中起作用的脾白细胞成分。我们的结果表明,在Lewis到ACI的低反应者组合中,向经亚致死剂量照射(全身照射200拉德)的ACI受体胸腺内接种静止的Lewis T细胞,始终能诱导对心脏同种异体移植的特异性无反应,在WF到Lewis的高反应者大鼠组合中也是如此,其中受体大鼠用抗淋巴细胞血清进行短暂免疫调节。相比之下,在同样制备的动物中,胸腺内接种供体B细胞、巨噬细胞或树突状细胞,在低反应者(Lewis到ACI)和高反应者(WF到Lewis)大鼠品系组合中均未能延长移植物存活时间。这一观察结果表明,通过胸腺内接种表达主要组织相容性(MHC)I类分子的供体型静止T细胞,而非任何表达MHC I类和II类分子的供体型抗原呈递细胞,可轻易实现供体特异性无反应。在短暂免疫抑制的受体中胸腺外接种T细胞未能防止移植物排斥,从而证明了胸腺在诱导耐受中的特殊地位。心脏同种异体移植的无反应受体特异性且永久地接受了供体型二次胰岛同种异体移植,从而证实了该模型中的抗原特异性耐受。这些结果表明,通过有意引入外来MHC I类细胞同种异体抗原,对发育中的T细胞进行胸腺再教育来操纵免疫系统,在诱导成年动物移植耐受方面具有治疗潜力。