Streilein J W, Wilbanks G A, Cousins S W
Department of Microbiology and Immunology, University of Miami School of Medicine, FL 33101.
J Neuroimmunol. 1992 Aug;39(3):185-200. doi: 10.1016/0165-5728(92)90253-h.
Immune-privileged sites, such as the the internal compartments of the eye, and perhaps the brain, are physiological adaptations that act to modify systemic immune responses such that effector mechanisms that invoke locally destructive inflammation are suppressed. In the case of the eye, the parenchymal cells of the iris and ciliary body create an intraocular microenvironment that alters both the induction and expression of immunity to antigens placed within the eye. The immunosuppressive properties of the intraocular microenvironment are mediated by cytokines, especially transforming growth factor-beta (TGF beta). This cytokine has been demonstrated to endow intraocular antigen-presenting cells with the capacity to induce an atypical or deviant form of immunity to intraocular antigens which is selectively deficient in T cells that mediate delayed hypersensitivity. Moreover, TGF beta, along with other intraocular factors, can impair the intraocular expression of pre-existing cell-mediated immunity by inhibiting antigen-driven activation of primed T cells. The strategies employed by the eye to engender specialized immune responses appropriate to its physiological functions are discussed in terms of other privileged sites such as the brain.
免疫赦免部位,如眼的内部腔室,或许还有脑,是生理适应性变化,其作用是改变全身免疫反应,从而抑制引发局部破坏性炎症的效应机制。就眼睛而言,虹膜和睫状体的实质细胞营造了一个眼内微环境,该微环境会改变对置于眼内抗原的免疫诱导和表达。眼内微环境的免疫抑制特性由细胞因子介导,尤其是转化生长因子-β(TGF-β)。已证实这种细胞因子能赋予眼内抗原呈递细胞诱导对眼内抗原的非典型或异常免疫形式的能力,这种免疫形式在介导迟发型超敏反应的T细胞中选择性缺乏。此外,TGF-β与其他眼内因子一起,可通过抑制抗原驱动的致敏T细胞活化,损害预先存在的细胞介导免疫在眼内的表达。本文将结合脑等其他特权部位,讨论眼睛为产生适合其生理功能的特殊免疫反应而采用的策略。