Murray P I, Rahi A H
Trans Ophthalmol Soc U K (1962). 1985;104 ( Pt 2):152-8.
Recent advances in the field of cellular immunology have enabled us to recognise a complex homeostatic mechanism controlling inflammation, allowing us to understand the aetiopathogenesis of many systemic disease processes. This immune regulatory mechanism involves the interaction of positive and negative messages passing between the different subsets of peripheral blood lymphocytes. Quantitative or qualitative defects in the suppressor cell subset of thymus derived T-lymphocytes are believed to be responsible (at least in part) for chronic inflammation and autoimmune disease. A variety of peripheral blood lymphocyte parameters were examined in four ill-understood inflammatory ophthalmological conditions: acute anterior uveitis, heterochromic cyclitis, acute lepromatous uveitis and Mooren's ulcer. Defects in the number or function of suppressor T-cells were found in all conditions studied. These findings make it possible to explain some of the immunological aberrations previously reported in these conditions. As abnormalities have been found in the immune regulatory mechanism of patients with inflammatory eye conditions of unknown aetiology, the way is now open to explore new lines of treatment using drugs which have the properties to allow selective manipulation of T-lymphocyte subsets.
细胞免疫学领域的最新进展使我们能够认识到一种控制炎症的复杂稳态机制,从而让我们理解许多全身性疾病过程的病因发病机制。这种免疫调节机制涉及外周血淋巴细胞不同亚群之间传递的正向和负向信息的相互作用。胸腺来源的T淋巴细胞抑制细胞亚群的定量或定性缺陷被认为(至少部分)是慢性炎症和自身免疫性疾病的原因。在四种了解较少的炎症性眼科疾病中检查了多种外周血淋巴细胞参数:急性前葡萄膜炎、异色性睫状体炎、急性瘤型麻风性葡萄膜炎和蚕食性角膜溃疡。在所研究的所有疾病中均发现抑制性T细胞数量或功能存在缺陷。这些发现使得能够解释先前在这些疾病中报道的一些免疫异常现象。由于在病因不明的炎症性眼病患者的免疫调节机制中发现了异常,现在有机会探索使用具有选择性操纵T淋巴细胞亚群特性的药物的新治疗方法。