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在Lewis大鼠中,酪氨酸酶相关蛋白1和2免疫诱导的眼内和眼外炎症。

Ocular and extraocular inflammation induced by immunization of tyrosinase related protein 1 and 2 in Lewis rats.

作者信息

Yamaki K, Kondo I, Nakamura H, Miyano M, Konno S, Sakuragi S

机构信息

Department of Ophthalmology, School of Medicine, Akita, Japan.

出版信息

Exp Eye Res. 2000 Oct;71(4):361-9. doi: 10.1006/exer.2000.0893.

Abstract

Vogt-Koyanagi-Harada (VKH) disease is an ocular inflammatory disease and is considered to be a cell-mediated, autoimmune disease against melanocytes. To learn more about the mechanisms involved in VKH disease, the identification of the antigens specific to the disease and the development of an animal model are critically important. We have expressed and purified the melanocyte specific proteins, tyrosinase-related protein 1 (TRP1) and 2 (TRP2). Lewis rats developed an ocular and extraocular inflammatory disease 12 days after immunization with TRP1 or TRP2 that was characterized clinically by the infiltration of inflammatory cells and accumulation of massive fibrin in the anterior and posterior chambers of the eye. Histologically, inflammatory cells were found in the anterior and posterior chambers, iris, ciliary body, the choroid, subretinal space and vitreous body. In severe cases, a serous detachment of the retina was observed. In mild cases, focal inflammatory lesions surrounded by normal chorioretinal architecture were observed and the inflammation persisted for more than 42 days after the injection. Some eyes showed accumulation of epithelioid cells in the choroid or the retinal pigment epithelium which were similar to the Dalen-Fuchs nodules found in patients with VKH disease. The alterations of the photoreceptor outer segment and the outer nuclear layer were less severe than in experimental autoimmune uveitis induced by retinal antigens. Extraocular manifestations such as skin lesions and meningitis were also observed. The clinical course and histological findings in these rats resembled the changes in patients with VKH disease.

摘要

伏格特-小柳-原田(VKH)病是一种眼部炎性疾病,被认为是一种针对黑素细胞的细胞介导的自身免疫性疾病。为了更深入了解VKH病所涉及的机制,鉴定该疾病特异性抗原以及建立动物模型至关重要。我们已经表达并纯化了黑素细胞特异性蛋白,酪氨酸酶相关蛋白1(TRP1)和2(TRP2)。用TRP1或TRP2免疫后的12天,Lewis大鼠出现了眼内和眼外炎性疾病,其临床特征为炎性细胞浸润以及眼内前房和后房大量纤维蛋白的积聚。组织学上,在前房、后房、虹膜、睫状体、脉络膜、视网膜下间隙和玻璃体中发现了炎性细胞。在严重的病例中,观察到视网膜浆液性脱离。在轻度病例中,观察到由正常脉络膜视网膜结构包围的局灶性炎性病变,并且在注射后炎症持续超过42天。一些眼睛在脉络膜或视网膜色素上皮中出现上皮样细胞积聚,这与VKH病患者中发现的Dalen-Fuchs结节相似。光感受器外段和外核层的改变不如视网膜抗原诱导的实验性自身免疫性葡萄膜炎严重。还观察到了皮肤病变和脑膜炎等眼外表现。这些大鼠的临床病程和组织学发现类似于VKH病患者的变化。

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