Doyle M V, Parks D E, Weigle W O
J Immunol. 1976 Jun;116(6):1640-5.
After adoptive transfer, the spleen cells from mice made tolerant to human gamma-globulin (HGG) specifically suppress the immune response of normal spleen cells. However, this suppressive activity in the spleen cells of tolerant mice is only present for a brief period after treatment with tolerogen. Spleen cells from animals injected 10 days earlier with tolerogen reduce the immune response of an equal number of normal spleen cells by 75%. Spleen cells from mice made tolerant 40 days previously are, however, no longer suppressive, even though they remain completely unresponsive. These data suggest that active suppression of antigen-reactive cells is not the mechanism responsible for maintaining tolerance to HGG, but rather is only transiently associated with the tolerant state. Further evidence in favor of the separation of the tolerant state from suppressive activity is that complete suppression of the normal spleen cell response requires either a high ratio of tolerant to immune competent cells or a delay in the antigenic challenge of the reconstituted recipients. By contrast, such manipulations are not required to demonstrate the complete unresponsiveness of the tolerant cells after adoptive transfer.
过继转移后,对人γ球蛋白(HGG)产生耐受的小鼠脾细胞可特异性抑制正常脾细胞的免疫反应。然而,耐受小鼠脾细胞中的这种抑制活性在用耐受原处理后仅在短时间内存在。10天前注射耐受原的动物的脾细胞可使等量正常脾细胞的免疫反应降低75%。然而,40天前产生耐受的小鼠的脾细胞不再具有抑制作用,尽管它们仍然完全无反应。这些数据表明,对抗抗原反应性细胞的主动抑制不是维持对HGG耐受的机制,而只是与耐受状态短暂相关。支持将耐受状态与抑制活性分离的进一步证据是,要完全抑制正常脾细胞反应,要么需要耐受细胞与免疫活性细胞的比例很高,要么需要延迟对重建受体的抗原攻击。相比之下,在过继转移后证明耐受细胞完全无反应则不需要进行此类操作。