首页> 美国卫生研究院文献>British Journal of Experimental Pathology >A murine model of experimental autoimmune lens-induced uveitis using Klebsiella O3 lipopolysaccharide as a potent immunological adjuvant.
【2h】

A murine model of experimental autoimmune lens-induced uveitis using Klebsiella O3 lipopolysaccharide as a potent immunological adjuvant.

机译:使用克雷伯菌O3脂多糖作为有效的免疫佐剂的实验性自身免疫性晶状体葡萄膜炎的小鼠模型。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Experimental autoimmune uveitis and finally panophthalmitis could be produced in mice by repeated immunization of syngeneic eyeball extract mixed with Klebsiella O3 lipopolysaccharide (KO3 LPS) as a powerful immunological adjuvant. No ocular lesions were produced in mice given eyeball extract emulsified in complete Freund's adjuvant (CFA), KO3 LPS alone or eyeball extract alone. Histopathological changes in the ocular lesions at the early stage after the second or tertiary immunization were characterized by infiltration with inflammatory cells in the ciliary body and iris. The iridocyclitis was followed by extensive infiltration of polymorphonuclear leucocytes (PMN) into the cornea, lens and the surrounding tissues after repeated immunization. Finally, these areas were replaced by granulomatous tissues infiltrated with mononuclear cells. On the other hand, the structure of the retina and sclera was partially preserved. Those mice exhibited production of autoantibodies and development of the delayed-type hypersensitivity (DTH) to syngeneic eyeball extract. Moreover, ocular lesions could be produced in normal recipient mice by transfer of sensitized lymphocytes from hyperimmunized mice. Therefore, it was suggested that the ocular lesions produced by repeated immunization with the mixture of eyeball extract and KO3 LPS were due to the autoimmune mechanism. This might be useful to model immunological phenomena in the pathogenesis of human phacoantigenic uveitis.
机译:通过对同种眼球提取物与克雷伯菌O3脂多糖(KO3 LPS)混合作为强力免疫佐剂进行重复免疫,可在小鼠中产生实验性自身免疫性葡萄膜炎和最后的全眼炎。给予完全弗氏佐剂(CFA),单独的KO3 LPS或单独的眼球提取物乳化的眼球提取物的小鼠未产生眼部损伤。第二次或三次免疫后早期眼部病变的组织病理学变化的特征是睫状体和虹膜中的炎性细胞浸润。虹膜睫状体炎后,反复免疫后,多形核白细胞(PMN)广泛浸入角膜,晶状体和周围组织。最后,这些区域被浸润了单核细胞的肉芽肿组织所代替。另一方面,视网膜和巩膜的结构被部分保留。这些小鼠表现出自身抗体的产生和对同源眼球提取物的迟发型超敏反应(DTH)的发展。此外,在正常的受体小鼠中,通过转移超免疫小鼠的致敏淋巴细胞可以产生眼部损伤。因此,建议通过用眼球提取物和KO3 LPS的混合物反复免疫产生的眼部损伤是由于自身免疫机制引起的。这可能对人类吞噬抗原性葡萄膜炎发病机理中的免疫学现象建模有用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号