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眼源性细胞因子与眼内免疫抑制微环境:综述

Eye-derived cytokines and the immunosuppressive intraocular microenvironment: a review.

作者信息

Streilein J W, Wilbanks G A, Taylor A, Cousins S

机构信息

Department of Microbiology and Immunology, University of Miami School of Medicine, FL.

出版信息

Curr Eye Res. 1992;11 Suppl:41-7. doi: 10.3109/02713689208999510.

Abstract

The normal aqueous humor contains a variety of soluble immunosuppressive factors, including transforming growth factor-beta, alpha-melanocyte stimulating hormone, and vasoactive intestinal peptide. These factors are largely the secretory products of parenchymal cells of the iris and ciliary body. TGF beta has recently been shown to alter the functional capacity of intraocular antigen presenting cells, such that they are capable of inducing Anterior Chamber Associated Immune Deviation (ACAID). This deviant systemic immune response is characterized by an impaired capacity to mount an effective cell-mediated immune attack directed at antigens that are placed in, or arise within, the eye. A second property of immunosuppressive factors in aqueous humor is to suppress directly the expression of delayed hypersensitivity in the anterior chamber. In fact, even when the intraocular microenvironment is disturbed by local instillation of gamma-interferon, making it possible for limited expression of cell-mediated immunity in the eye, the microenvironment of the anterior chamber remains profoundly immunosuppressive. In this latter instance, prostaglandins replace TGF beta as the major molecular mediators of suppression in the aqueous humor. In the aggregate, factors present in the normal (or perturbed) intraocular microenvironment have the capacity to modify both the afferent and efferent limbs of the systemic immune response, and this accounts for the longstanding observation that the anterior chamber is an immunologically privileged site. Since evidence suggests that the eye can mobilize more than one molecular mechanism in its effort to limit the sight-destroying potential of immunogenic inflammation, we believe that elucidation of intraocular cytokines and factors that create and maintain an immunosuppressive microenvironment will contribute to a better understanding of the pathogenesis of the acute and chronic uveitides, especially those of autoimmune and infectious etiology.

摘要

正常房水中含有多种可溶性免疫抑制因子,包括转化生长因子-β、α-黑素细胞刺激素和血管活性肠肽。这些因子主要是虹膜和睫状体实质细胞的分泌产物。最近研究表明,转化生长因子-β可改变眼内抗原呈递细胞的功能,使其能够诱导前房相关免疫偏离(ACAID)。这种异常的全身免疫反应的特征是针对眼内植入或产生的抗原进行有效细胞介导免疫攻击的能力受损。房水中免疫抑制因子的另一个特性是直接抑制前房迟发型超敏反应的表达。事实上,即使眼内微环境因局部滴注γ-干扰素而受到干扰,使得眼内细胞介导免疫有有限表达的可能,前房的微环境仍具有很强的免疫抑制作用。在后一种情况下,前列腺素取代转化生长因子-β成为房水中主要的抑制分子介质。总体而言,正常(或受干扰)眼内微环境中存在的因子有能力改变全身免疫反应的传入和传出环节,这就解释了长期以来观察到的前房是一个免疫赦免部位的现象。由于有证据表明,眼睛可以调动不止一种分子机制来限制免疫原性炎症对视力的破坏潜力,我们认为阐明眼内细胞因子以及产生和维持免疫抑制微环境的因子,将有助于更好地理解急性和慢性葡萄膜炎的发病机制,尤其是那些自身免疫性和感染性病因的葡萄膜炎。

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