Caspi R R, Kuwabara T, Nussenblatt R B
Laboratory of Immunology, National Eye Institute, Bethesda, MD 20892.
J Immunol. 1988 Apr 15;140(8):2579-84.
A Ts lymphocyte line was isolated from spleens of rats primed with the retinal soluble Ag (SAg) in the anterior chamber of the eye. This line could inhibit in vitro SAg-driven proliferation of uveitogenic Th lymphocytes, in a radioresistant, Ag-independent manner. Adoptively transferred Ts line cells were found to downgrade experimental autoimmune uveoretinitis in actively immunized syngeneic recipients. The initial surface phenotype (OX8+) of the Ts line was unstable in vitro, however, the cells expressed suppressor function irrespective of phenotype. The mechanism of suppression did not appear to involve consumption of IL-2 or direct cytolysis of uveitogenic Th lymphocytes, but rather the production of a soluble suppressor factor. These findings may suggest an in vivo role for suppressor lymphocytes, capable of inhibiting primed Th cells, in the regulation of experimental autoimmune uveoretinitis.
从经眼眼前房内视网膜可溶性抗原(SAg)致敏的大鼠脾脏中分离出一个 Ts 淋巴细胞系。该细胞系能够以抗辐射、抗原非依赖的方式,在体外抑制致葡萄膜炎性 Th 淋巴细胞由 SAg 驱动的增殖。发现过继转移的 Ts 细胞系细胞可使主动免疫的同基因受体中的实验性自身免疫性葡萄膜视网膜炎病情减轻。Ts 细胞系最初的表面表型(OX8+)在体外不稳定,然而,无论表型如何,这些细胞均表达抑制功能。抑制机制似乎不涉及 IL-2 的消耗或致葡萄膜炎性 Th 淋巴细胞的直接细胞溶解,而是可溶性抑制因子的产生。这些发现可能提示抑制性淋巴细胞在体内对实验性自身免疫性葡萄膜视网膜炎的调节中具有抑制已致敏 Th 细胞的作用。