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首页> 外文期刊>Clinical & developmental immunology. >Impaired Fas-Fas Ligand Interactions Result in Greater Recurrent Herpetic Stromal Keratitis in Mice
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Impaired Fas-Fas Ligand Interactions Result in Greater Recurrent Herpetic Stromal Keratitis in Mice

机译:Fas-Fas配体相互作用减弱导致小鼠复发性疱疹性基质性角膜炎复发率更高

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Herpes simplex virus-1 (HSV-1) infection of the cornea leads to a potentially blinding condition termed herpetic stromal keratitis (HSK). Clinical studies have indicated that disease is primarily associated with recurrent HSK following reactivation of a latent viral infection of the trigeminal ganglia. One of the key factors that limit inflammation of the cornea is the expression of Fas ligand (FasL). We demonstrate that infection of the cornea with HSV-1 results in increased functional expression of FasL and that mice expressing mutations in Fas (Ipr) and FasL (gld) display increased recurrent HSK following reactivation compared to wild-type mice. Furthermore, both gld and Ipr mice took longer to clear their corneas of infectious virus and the reactivation rate for these strains was significantly greater than that seen with wild-type mice. Collectively, these findings indicate that the interaction of Fas with FasL in the cornea restricts the development of recurrent HSK.
机译:角膜的单纯疱疹病毒1(HSV-1)感染会导致潜在的致盲性疾病,称为疱疹性基质性角膜炎(HSK)。临床研究表明,该疾病主要与三叉神经节的潜在病毒感染重新激活后复发的HSK有关。限制角膜炎症的关键因素之一是Fas配体(FasL)的表达。我们证明,用HSV-1感染角膜会导致FasL的功能性表达增加,并且与野生型小鼠相比,激活后在Fas(Ipr)和FasL(gld)中表达突变的小鼠显示出增加的复发性HSK。此外,gld和Ipr小鼠都需要花费更长的时间清除其角膜上的传染性病毒,而且这些菌株的再激活率显着高于野生型小鼠。总的来说,这些发现表明Fas与角膜中FasL的相互作用限制了复发性HSK的发展。

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