Kawashima H, Fujino Y, Mochizuki M
Department of Ophthalmology, School of Medicine University of Tokyo, Japan.
Invest Ophthalmol Vis Sci. 1990 Dec;31(12):2500-7.
The authors previously reported that FK506 effectively suppressed the induction of experimental autoimmune uveoretinitis (EAU) in rats with much lower doses than cyclosporine A. This study was aimed at analyzing the immune status of the FK506-treated and EAU-suppressed rats and examining the hypothesis whether the agent could induce antigen-specific suppressor T (Ts) cells. It was found that spleens from S-antigen-immunized and FK506-treated rats contained a population of Ts cells inhibiting the proliferative responses of S-antigen-sensitized lymphocytes to S-antigen, yet these cells did not affect the proliferative responses of interphotoreceptor retinoid-binding protein (IRBP)-sensitized lymphocytes to IRBP. The helper T (Th) cells did not exhibit such suppressor activities. Furthermore, transfer of Ts cells from S-antigen-immunized and FK506-treated rats to naive syngenic rats induced partial inhibition of EAU induction or delay of EAU onset after immunizing the recipient rats with S-antigen. Lymphocytes from the EAU-suppressed recipients showed low proliferative response to S-antigen and low levels of antibody to S-antigen. These data thus indicate that FK506 treatment after S-antigen immunization induces an activation of Ts cells specific to S-antigen and that the Ts cells might contribute, at least in part, to the uniquely prolonged and intensive immunosuppression by FK506.
作者之前报道,与环孢素A相比,FK506以低得多的剂量就能有效抑制大鼠实验性自身免疫性葡萄膜视网膜炎(EAU)的诱发。本研究旨在分析经FK506治疗且EAU得到抑制的大鼠的免疫状态,并检验该药物是否能诱导抗原特异性抑制性T(Ts)细胞这一假说。结果发现,来自经S抗原免疫并接受FK506治疗的大鼠的脾脏含有一群Ts细胞,这些细胞可抑制S抗原致敏淋巴细胞对S抗原的增殖反应,但这些细胞并不影响光感受器间类视黄醇结合蛋白(IRBP)致敏淋巴细胞对IRBP的增殖反应。辅助性T(Th)细胞未表现出这种抑制活性。此外,将经S抗原免疫并接受FK506治疗的大鼠的Ts细胞转移至同基因的未致敏大鼠,在用S抗原免疫受体大鼠后,可诱导EAU诱发受到部分抑制或EAU发病延迟。来自EAU得到抑制的受体的淋巴细胞对S抗原的增殖反应较低,且针对S抗原的抗体水平也较低。因此,这些数据表明,S抗原免疫后进行FK506治疗可诱导S抗原特异性Ts细胞的激活,且Ts细胞可能至少部分促成了FK506独特的长期且强效的免疫抑制作用。