Kapp J A, Jensen P E, Robbins P F, Fritschle C
J Immunol. 1984 Dec;133(6):2888-91.
Murine antibody responses to heterologous insulins are under H-2-linked immune response (Ir) gene control. We previously demonstrated that the immune response to insulin in Freund's complete adjuvant (CFA) can be specifically inhibited by prior injection of soluble insulin i.v. Unresponsiveness requires at least 4 days after i.v. injection to develop, and once induced, it lasts 4 wk or more. Unresponsiveness is caused by T cell, but not B cell, tolerance; furthermore, we have been unable to demonstrate any role for suppressor T cells in this unresponsiveness. The following experiments examine the nature of the T cell tolerance induced by i.v. injection of insulin, and the data suggest that helper T cells were not clonally deleted by this procedure. The functional activity of the tolerized T cells can be rescued by stimulation with insulin covalently complexed to the type 1 T-independent (TI-1) antigen, Brucella abortus. This observation suggests that tolerance induced by soluble insulin is due to clonal anergy rather than clonal deletion of helper T cells; thus, this system could provide a model for determining the cellular events involved in tolerance induction and reversal in helper T cells.
小鼠对异源胰岛素的抗体反应受H-2连锁免疫反应(Ir)基因控制。我们先前证明,静脉注射可溶性胰岛素可特异性抑制弗氏完全佐剂(CFA)中对胰岛素的免疫反应。无反应性在静脉注射后至少需要4天才能形成,一旦诱导形成,可持续4周或更长时间。无反应性是由T细胞而非B细胞耐受引起的;此外,我们未能证明抑制性T细胞在这种无反应性中起任何作用。以下实验研究了静脉注射胰岛素诱导的T细胞耐受的性质,数据表明辅助性T细胞并未通过该程序发生克隆性缺失。用与1型非T细胞依赖性(TI-1)抗原流产布鲁氏菌共价结合的胰岛素刺激可挽救耐受T细胞的功能活性。这一观察结果表明,可溶性胰岛素诱导的耐受是由于克隆无能而非辅助性T细胞的克隆性缺失;因此,该系统可为确定辅助性T细胞耐受诱导和逆转过程中涉及的细胞事件提供一个模型。