Ferguson T A, Waldrep J C, Kaplan H J
J Immunol. 1987 Jul 15;139(2):352-7.
We studied the cellular basis for the induction of Ts cells in anterior chamber (AC)-associated immune deviation (ACAID) by using TNP-modified syngeneic spleen cells (TNP-Spl). We demonstrate that the cells responsible for the induction of TNP-ACAID are non adherent, IA- T cells. This is in contrast to the antigen-presenting cells which induce suppression after the i.v. injection of TNP-Spl which are IA+/I-J+ adherent cells. Furthermore, two T cells within the TNP-Spl population are required to initiate suppression in TNP-ACAID: one is Lyt-1+, and I-J+, the other is Lyt-1+ and reactive with a monoclonal antibody, 14-30, which specifically identifies Ts inducer cells. The antigen specificity of ACAID resides in the 14-30+ T cell, and not the I-J+ cell. Although both cells must be viable to induce suppression, neither they (nor their products) must be in direct contact within the eye; one population may be in the right AC, the other in the left. Our results suggest that it is Ts inducer cells placed into the AC of the eye which initiate TNP-ACAID, and that these cells exit (or secrete Ts factors which exit) the eye to induce Ts effector cells in the spleen.
我们通过使用经三硝基苯(TNP)修饰的同基因脾细胞(TNP-Spl),研究了前房(AC)相关免疫偏离(ACAID)中 Ts 细胞诱导的细胞基础。我们证明,负责诱导 TNP-ACAID 的细胞是非黏附性、IA-的 T 细胞。这与静脉注射 TNP-Spl 后诱导抑制的抗原呈递细胞形成对比,后者是 IA+/I-J+黏附细胞。此外,TNP-Spl 群体中的两种 T 细胞对于启动 TNP-ACAID 中的抑制作用是必需的:一种是 Lyt-1+、I-J+,另一种是 Lyt-1+且与单克隆抗体 14-30 反应,该抗体可特异性识别 Ts 诱导细胞。ACAID 的抗原特异性存在于 14-30+ T 细胞中,而非 I-J+细胞。尽管两种细胞都必须存活才能诱导抑制,但它们(及其产物)在眼内不必直接接触;一种细胞群体可以在右眼房,另一种在左眼房。我们的结果表明,是置于眼房中的 Ts 诱导细胞启动了 TNP-ACAID,并且这些细胞离开(或分泌离开眼的 Ts 因子)眼以在脾脏中诱导 Ts 效应细胞。