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环孢素A对单纯疱疹病毒性角膜炎角膜炎症反应的影响。

Effect of cyclosporine A on the corneal inflammatory response in herpes simplex virus keratitis.

作者信息

Meyers-Elliott R H, Chitjian P A, Billups C L

机构信息

Jules Stein Eye Institute, UCLA School of Medicine 90024.

出版信息

Exp Eye Res. 1987 Aug;45(2):281-303. doi: 10.1016/s0014-4835(87)80151-3.

Abstract

The effects of cyclosporine A (CyA), a selective inhibitor of T-lymphocyte function, on the corneal inflammatory response in herpes simplex virus (HSV) stromal keratitis was followed during the course of experimental HSV keratitis in the rabbit. The corneal response, characterized by polymorphonuclear leukocytes (PMN) and mononuclear cells, is an immunologically specific event that is dependent on the presence of viral antigens and immune cells. CyA treatment during the course of HSV keratitis resulted in a more severe and persistent stromal disease and more anterior chamber involvement than that seen in the solvent control-treated HSV-infected animals. Clinical observations correlated well with histological studies which confirmed a greater incidence of mononuclear and PMN infiltrates throughout the anterior chamber and stroma in the CyA-treated animals. HSV antigens were present in the corneas from both infected groups as observed by immunofluorescence staining, but endothelial localization of HSV antigens was seen primarily in the CyA-treated animals, often accompanied by cells in the anterior chamber. No significant differences in IgG and IgM staining in the diseased corneas and anterior chamber were noted between the CyA-treated and solvent control groups which suggests that there was no local B-cell immunosuppression.

摘要

在兔实验性单纯疱疹病毒(HSV)角膜炎过程中,观察了T淋巴细胞功能选择性抑制剂环孢素A(CyA)对HSV基质性角膜炎角膜炎症反应的影响。以多形核白细胞(PMN)和单核细胞为特征的角膜反应是一种免疫特异性事件,它依赖于病毒抗原和免疫细胞的存在。与溶剂对照处理的HSV感染动物相比,在HSV角膜炎过程中用CyA治疗导致更严重和持久的基质疾病以及更多的前房受累。临床观察结果与组织学研究结果密切相关,组织学研究证实,在接受CyA治疗的动物中,整个前房和基质中单核细胞和PMN浸润的发生率更高。通过免疫荧光染色观察到,两个感染组的角膜中均存在HSV抗原,但HSV抗原的内皮定位主要见于接受CyA治疗的动物,且常伴有前房中的细胞。在接受CyA治疗的组和溶剂对照组之间,患病角膜和前房中IgG和IgM染色没有显著差异,这表明不存在局部B细胞免疫抑制。

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