Systemic IL-1β production as a consequence of corneal HSV-1 infection-contribution to the development of herpes simplex keratitis

被引:1
作者
Joan Ní Gabhann-Dromgoole [1 ,2 ]
Ciaran de Chaumont [1 ,2 ]
David Shahnazaryan [2 ,3 ]
Siobhán Smith [1 ]
Conor Malone [2 ,3 ]
Jaythoon Hassan [4 ]
Cillian F.De Gascun [4 ]
Caroline A.Jefferies [1 ,5 ]
Conor C.Murphy [2 ,3 ]
机构
[1] Molecular and Cellular Therapeutics and RSCI Research Institute, Royal College of Surgeons in Ireland
[2] Department of Ophthalmology, Royal College of Surgeons in Ireland
[3] Department of Ophthalmology, Royal Victoria Eye and Ear Hospital
[4] National Virus Reference Laboratory, University College Dublin
[5] Department of Medicine, Division of Rheumatology and Department of Biomedical Sciences, Cedars-Sinai Medical Centre
关键词
herpes simplex virus type 1; herpes simplex keratitis; inflammation; peripheral immune response; pathogenesis;
D O I
暂无
中图分类号
R772.21 [角膜炎、角膜溃疡];
学科分类号
100212 ;
摘要
This study sought to identify potential therapeutic targets in herpes simplex keratitis(HSK) patients with active and inactive infection by investigating peripheral cytokine production. Peripheral blood mononuclear cells(PBMCs) and serum were prepared from healthy controls and HSK patients during active infection or following treatment(inactive infection). Serum antibody titres were determined by ELISA. Protein expression levels were analysed by Western blot. Cytokine levels were determined by multiplex ELISA. Active corneal herpes simplex virus type 1(HSV-1) infection resulted in significantly elevated peripheral levels of IL-1β in HSK patients compared to healthy controls, and remained significantly increased following treatment. Elevated production of IL-1β in inactive patients was associated with significantly increased levels of IRF3 and STAT1, key proteins involved in promoting anti-viral immune responses. Our data suggest that inflammation persists beyond the period that it is clinically evident and that enhanced peripheral production of IL-1β may have implications for HSV-1 viral clearance in active and inactive HSK patients.
引用
收藏
页码:1493 / 1497
页数:5
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