Murray P I, Mooy C M, Visser-de Jong E, Baarsma G S, de Vries P T, de Jong V M, Kijlstra A
Department of Ophthalmo-Immunology, Netherlands Ophthalmic Research Institute, Amsterdam.
Am J Ophthalmol. 1990 Apr 15;109(4):394-9. doi: 10.1016/s0002-9394(14)74604-5.
Using immunohistochemical techniques, we analyzed iris biopsy specimens from eight patients with Fuchs' heterochromic cyclitis, seven patients with various other types of uveitis, and eight glaucoma patients without uveitis. No specific abnormalities related to Fuchs' heterochromic cyclitis could be detected. Four of the patients with Fuchs' heterochromic cyclitis and four of the patients with uveitis showed evidence of an inflammatory cell infiltrate, which was a mixture of interleukin-2 receptor-negative T helper and suppressor cells, B lymphocytes, and plasma cells. Only an occasional T lymphocyte could be seen in two of the patients without uveitis. The class II antigen HLA-DR was expressed on iris stromal cells in every patient in the Fuchs' heterochromic cyclitis group and uveitis group and in six of the patients in the nonuveitis group. In six of the Fuchs' heterochromic cyclitis patients, including two without immunohistochemical evidence of inflammatory cell infiltrate, histologic abnormalities were present on hematoxylin and eosin sections.
我们运用免疫组化技术,分析了8例Fuchs异色性睫状体炎患者、7例其他各类葡萄膜炎患者以及8例无葡萄膜炎的青光眼患者的虹膜活检标本。未检测到与Fuchs异色性睫状体炎相关的特异性异常。4例Fuchs异色性睫状体炎患者和4例葡萄膜炎患者有炎症细胞浸润的证据,浸润细胞包括白细胞介素-2受体阴性的辅助性T细胞和抑制性T细胞、B淋巴细胞及浆细胞。在2例无葡萄膜炎的患者中仅偶尔可见T淋巴细胞。Fuchs异色性睫状体炎组和葡萄膜炎组的每位患者以及非葡萄膜炎组的6例患者的虹膜基质细胞均表达II类抗原HLA-DR。在6例Fuchs异色性睫状体炎患者中,包括2例无免疫组化证据显示炎症细胞浸润的患者,苏木精-伊红染色切片存在组织学异常。