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伏格特-小柳-原田综合征、白塞病和交感性眼炎中的抗视网膜自身抗体。

Anti-retinal auto-antibodies in Vogt-Koyanagi-Harada syndrome, Behcet's disease, and sympathetic ophthalmia.

作者信息

Chan C C, Palestine A G, Nussenblatt R B, Roberge F G, Benezra D

出版信息

Ophthalmology. 1985 Aug;92(8):1025-8. doi: 10.1016/s0161-6420(85)33911-8.

Abstract

Sera of patients diagnosed as having the active Vogt-Koyanagi-Harada (VKH) syndrome, Behcet's syndrome or sympathetic ophthalmia as well as normal controls were evaluated by ELISA and by staining of normal human retinal tissue using the avidin-biotin-peroxidase complex (ABC) technique for anti-retinal antibodies. No anti-retinal S-antigen antibodies were detected by ELISA. However, autoimmune antibodies were found against the outer segments of photoreceptors and Müller cells in patients with the VKH syndrome, with lower titers in some patients with Behcet's syndrome, and in a few patients with sympathetic ophthalmia. These results suggested anti-retinal antibodies were present and that retinal autoimmunity may play a role in pathogenesis in varieties of posterior uveitis. In addition, the indirect immunoperoxidase staining technique may facilitate the diagnosis of VKH in uncertain cases.

摘要

采用酶联免疫吸附测定(ELISA)以及运用抗生物素蛋白-生物素-过氧化物酶复合物(ABC)技术对正常人视网膜组织进行抗视网膜抗体染色的方法,对被诊断患有活动性Vogt-小柳-原田(VKH)综合征、贝赫切特综合征或交感性眼炎的患者血清以及正常对照血清进行了评估。通过ELISA未检测到抗视网膜S抗原抗体。然而,在VKH综合征患者中发现了针对光感受器外段和Müller细胞的自身抗体,在部分贝赫切特综合征患者中抗体滴度较低,在少数交感性眼炎患者中也有发现。这些结果表明存在抗视网膜抗体,并且视网膜自身免疫可能在多种后葡萄膜炎的发病机制中起作用。此外,间接免疫过氧化物酶染色技术可能有助于在不确定的病例中诊断VKH综合征。

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