Shtein Roni M, Elner Victor M
Department of Ophthalmology and Visual Sciences, University of Michigan, Kellogg Eye Center, 1000 Wall Street, Ann Arbor, MI 48105, USA, Tel.: +1 734 763 5506, ,
Expert Rev Ophthalmol. 2010 Apr 1;5(2):129-134. doi: 10.1586/eop.10.12.
Molecular biologic studies have elucidated the roles of specific and innate immune responses in the pathogenesis of HSV keratitis. Recent evidence suggests that interference with innate immune mechanisms may reduce the severity of HSV keratitis and its complications. The agents targeting innate immune responses are particularly amenable to translational therapy for patients at risk of complications of HSV keratitis and poor corneal transplant outcomes. Histopathologic evidence of neovascularization or inflammation in tissue removed at the time of corneal transplantation predicts patients who are at risk for allograft rejection or failure. Such patients are prime candidates for close monitoring and intensive therapy. Newer imaging techniques, such as clinical confocal biomicroscopy, might be useful in identifying neovascularization and inflammation that place patients at high risk for poor allograft outcomes prior to corneal transplantation.
分子生物学研究已经阐明了特异性免疫反应和固有免疫反应在单纯疱疹病毒性角膜炎发病机制中的作用。最近的证据表明,干扰固有免疫机制可能会减轻单纯疱疹病毒性角膜炎及其并发症的严重程度。针对固有免疫反应的药物特别适合用于对单纯疱疹病毒性角膜炎并发症风险高和角膜移植效果差的患者进行转化治疗。角膜移植时切除的组织中新生血管形成或炎症的组织病理学证据可预测患者发生同种异体移植排斥或失败的风险。这类患者是密切监测和强化治疗的主要候选对象。更新的成像技术,如临床共焦生物显微镜检查,可能有助于在角膜移植前识别使患者发生同种异体移植不良后果风险高的新生血管形成和炎症。