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Onchocerciasis: experimental models of ocular disease.

作者信息

Donnelly J J, Rockey J H, Taylor H R, Soulsby E J

出版信息

Rev Infect Dis. 1985 Nov-Dec;7(6):820-5. doi: 10.1093/clinids/7.6.820.

DOI:10.1093/clinids/7.6.820
PMID:4070920
Abstract

Onchocerciasis is a leading cause of blindness in equatorial Africa and in endemic regions in Central America. Understanding of the pathologic processes involved in onchocercal eye disease and of the role of immunopathologic mechanisms in its development has been substantially limited by the shortage of eyes for histologic study and by the lack of a naturally occurring animal model. The inoculation of microfilariae of Onchocerca species into the eyes of laboratory animals may reproduce selected aspects of onchocercal eye disease, such as punctate keratitis. Studies in these models support the hypothesis that immunopathologic mechanisms mediated by IgE antibody are involved in the development of ocular lesions. In some laboratory animal models, diethylcarbamazine citrate, a microfilaricidal drug that causes severe inflammatory reactions to microfilariae in humans, increases the severity of ocular lesions, and stimulates IgE antibody responses. Laboratory animal studies are potentially highly useful for understanding the immunopathogenesis of ocular onchocerciasis.

摘要

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引用本文的文献

1
Interleukin 4 and T helper type 2 cells are required for development of experimental onchocercal keratitis (river blindness).实验性盘尾丝虫性角膜炎(河盲症)的发展需要白细胞介素4和2型辅助性T细胞。
J Exp Med. 1995 Oct 1;182(4):931-40. doi: 10.1084/jem.182.4.931.
2
Immunological crossreactivity between a cloned antigen of Onchocerca volvulus and a component of the retinal pigment epithelium.盘尾丝虫克隆抗原与视网膜色素上皮成分之间的免疫交叉反应性。
J Exp Med. 1991 Jul 1;174(1):169-77. doi: 10.1084/jem.174.1.169.