Experimental coronavirus retinopathy (ECOR): Retinal degeneration susceptible mice have an augmented interferon and chemokine (CXCL9, CXCL10) response early after virus infection

被引:15
作者
Detrick, Barbara [1 ]
Lee, Maria Teresa
Chin, Marian S.
Hooper, Laura C.
Chan, Chi-Chao
Hooks, John J.
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21287 USA
关键词
coronavirus; retinal degeneration; chemokines; interferon; autoimmunity;
D O I
10.1016/j.jneuroim.2007.09.032
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mouse hepatitis virus induces a biphasic disease in BALB/c mice that consists of an acute retinitis followed by progression to a chronic retinal degeneration with autoimmune reactivity. Retinal degeneration resistant CD-1 mice do not develop the late phase. What host factors contribute to the distinct responses to the virus are unknown. Herein, we show that IFN-alpha, IFN-beta and IFN-gamma act in concert as part of the innate immune response to the retinal infection. At day 2, high serum levels of IFN-gamma, CXCL9 and CXCL10, were detected in BALB/c mice. Moreover, elevated levels of CXCL9 and CXCL 10 gene expression were detected in retinal tissue. Although IFN-gamma and the chemokines were detected in CD-1 mice, they were at significantly lower levels compared to BALB/c mice. These augmented innate responses observed correlated with the development of autoimmune reactivity and retinal degeneration and thus may contribute to the pathogenic processes. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 37
页数:10
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