Gao E K, Lo D, Sprent J
Department of Immunology, Research Institute of Scripps Clinic, La Jolla, California 92037.
J Exp Med. 1990 Apr 1;171(4):1101-21. doi: 10.1084/jem.171.4.1101.
T cell tolerance induction was examined in long-term H-2-heterozygous parent----F1 chimeras prepared with supralethal irradiation (1,300 rad). Although these chimeras appeared to be devoid of host-type APC, the donor T cells developing in the chimeras showed marked tolerance to host-type H-2 determinants. Tolerance to the host appeared to be virtually complete in four assay systems: (a) primary mixed lymphocyte reactions (MLR) of purified lymph node (LN) CD8+ cells (+/- IL-2); (b) primary MLR of CD4+ (CD8-) thymocytes; (c) skin graft rejection; and (d) induction of lethal graft-vs.-host disease by CD4+ cells. Similar tolerance was observed in chimeras given double irradiation. The only assay in which the chimera T cells failed to show near-total tolerance to the host was the primary MLR of post-thymic CD4+ cells. In this assay, LN CD4+ cells regularly gave a significant antihost MLR. The magnitude of this response was two- to fourfold less than the response of normal parental strain CD4+ cells and, in I-E(-)----I-E+ chimeras, was paralleled by approximately 70% deletion of V beta 11+ cells. Since marked tolerance was evident at the level of mature thymocytes, tolerance induction in the chimeras presumably occurred in the thymus itself. The failure to detect host APC in the thymus implies that tolerance reflected contact with thymic epithelial cells (and/or other non-BM-derived cells in the thymus). To account for the residual host reactivity of LN CD4+ cells and the incomplete deletion of V beta 11+ cells, it is suggested that T cell contact with thymic epithelial cells induced clonal deletion of most of the host-reactive T cells but spared a proportion of these cells (possibly low affinity cells). Since these latter cells appeared to be functionally inert in the thymus (in contrast to LN), we suggest that the thymic epithelial cells induced a temporary form of anergy in the remaining host-reactive thymocytes. This anergic state disappeared when the T cells left the thymus and reached LN.
在用超致死剂量照射(1300拉德)制备的长期H-2杂合亲代-F1嵌合体中检测了T细胞耐受诱导情况。尽管这些嵌合体似乎缺乏宿主型抗原呈递细胞(APC),但在嵌合体中发育的供体T细胞对宿主型H-2决定簇表现出明显的耐受性。在四个检测系统中,对宿主的耐受性似乎几乎是完全的:(a)纯化的淋巴结(LN)CD8+细胞(±白细胞介素-2)的初次混合淋巴细胞反应(MLR);(b)CD4+(CD8-)胸腺细胞的初次MLR;(c)皮肤移植排斥反应;以及(d)CD4+细胞诱导的致死性移植物抗宿主病。在接受双重照射的嵌合体中也观察到了类似的耐受性。嵌合体T细胞对宿主未能表现出近乎完全耐受性的唯一检测是胸腺后CD4+细胞的初次MLR。在该检测中,LN CD4+细胞通常会产生显著的抗宿主MLR。这种反应的强度比正常亲代菌株CD4+细胞的反应低两到四倍,并且在I-E(-)----I-E+嵌合体中,伴随着约70%的Vβ11+细胞缺失。由于在成熟胸腺细胞水平上明显存在显著的耐受性,嵌合体中的耐受诱导可能发生在胸腺本身。在胸腺中未能检测到宿主APC意味着耐受性反映了与胸腺上皮细胞(和/或胸腺中其他非骨髓来源的细胞)的接触。为了解释LN CD4+细胞的残留宿主反应性和Vβ11+细胞的不完全缺失,有人提出T细胞与胸腺上皮细胞的接触诱导了大多数宿主反应性T细胞的克隆清除,但保留了一部分这些细胞(可能是低亲和力细胞)。由于这些后一种细胞在胸腺中似乎功能惰性(与LN相反),我们认为胸腺上皮细胞在剩余的宿主反应性胸腺细胞中诱导了一种暂时的无反应状态。当T细胞离开胸腺到达LN时,这种无反应状态消失。