Department of Ophthalmology, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Department of Ophthalmology & Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Immunol Res. 2015;2015:435140. doi: 10.1155/2015/435140. Epub 2015 Oct 4.
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 (lpr) and FasL (gld) display increased recurrent HSK following reactivation compared to wild-type mice. Furthermore, both gld and lpr 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.
单纯疱疹病毒-1(HSV-1)感染角膜可导致潜在致盲性疾病,称为疱疹性基质角膜炎(HSK)。临床研究表明,疾病主要与三叉神经节潜伏病毒感染再激活后复发性 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,HSV-1 感染角膜可导致 FasL 的功能性表达增加,并且与野生型小鼠相比,表达 Fas(lpr)和 FasL(gld)突变的小鼠在再激活后显示出复发性 HSK 增加。此外,gld 和 lpr 小鼠清除角膜感染性病毒的时间更长,这些菌株的再激活率明显高于野生型小鼠。总之,这些发现表明 Fas 与角膜 FasL 的相互作用限制了复发性 HSK 的发展。