Mowat A M, Lamont A G, Parrott D M
Department of Bacteriology and Immunology, Western Infirmary, Glasgow, U.K.
Immunology. 1988 May;64(1):141-5.
Suppressor T cells (Ts) and antigen-presenting cell (APC) activity are both important for the induction of systemic tolerance after feeding protein antigens to mice. In this report, we have examined further the nature of the inter-relationship between Ts and APC in oral tolerance to ovalbumin (OVA). We found previously that oral tolerance to OVA could prevented by treating mice with oestradiol, and we now report that oestradiol enhances the ability of spleen APC to present OVA to T cells. In parallel, mice treated with oestradiol do not generate the Ts activity normally found after feeding OVA. Treatment of mice with anti-I-J antiserum prevents the induction of both tolerance and Ts activity after feeding OVA, but the suppressor effector cells generated by feeding OVA can not be depleted in vitro by treatment with anti-I-J antibody plus complement. In vivo administration of monoclonal anti-I-A antibody had no effect on oral tolerance to OVA. Our results show that induction of oral tolerance to OVA is an I-J-restricted phenomenon and we propose that this reflects an interaction between specific Ts cells and a population of I-J+ cells which we suggest are APC.
抑制性T细胞(Ts)和抗原呈递细胞(APC)的活性对于给小鼠喂食蛋白质抗原后诱导全身耐受性都很重要。在本报告中,我们进一步研究了在卵清蛋白(OVA)口服耐受中Ts与APC之间相互关系的本质。我们先前发现,用雌二醇处理小鼠可预防对OVA的口服耐受,现在我们报告雌二醇可增强脾脏APC将OVA呈递给T细胞的能力。同时,用雌二醇处理的小鼠不会产生喂食OVA后通常会出现的Ts活性。用抗I-J抗血清处理小鼠可防止喂食OVA后诱导耐受性和Ts活性,但喂食OVA产生的抑制效应细胞不能通过用抗I-J抗体加补体在体外耗尽。体内给予单克隆抗I-A抗体对OVA的口服耐受没有影响。我们的结果表明,对OVA的口服耐受诱导是一种I-J限制现象,我们提出这反映了特定Ts细胞与一群我们认为是APC的I-J +细胞之间的相互作用。