Novel Therapies to Prevent Blindness Caused by Proliferative Vitreoretinopathy

描述（由申请人提供）：增殖性玻璃体视网膜病变（PVR）发生在视网膜脱离和严重眼外伤后，导致视网膜前和视网膜下瘢痕形成，这是这些患者预后不良的主要决定因素之一。重要的是，PVR可能在超过50%的穿孔损伤患者和高达10%的视网膜脱离患者中发现。尽管PVR的病理生理机制尚不完全清楚，但目前的证据表明，包括视网膜色素上皮（RPE）在内的多种细胞类型参与了异常的伤口愈合反应。这项工作的长期目标是制定一种新的策略来有效地预防或治疗这种反应，以降低PVR导致失明或永久性视力丧失的风险。这项建议与健康的关系是，这项工作的成功完成可能会导致受影响个体的视力保留。最近的研究支持这样的假设，即控制上皮膜蛋白2（上皮膜蛋白2）或其下游信号通路可能改变RPE细胞的生物学反应并预防或治疗PVR。在本次申请中提出的具体目标将验证以下假设：下调EMP2或其信号转导途径可能在体外和体内疾病动物模型中有效预防或治疗PVR。三种不同的方法将用于动物模型，包括目前用于癌症治疗的抑制剂，我们实验室开发的设计抗体，以及生化途径的小分子抑制剂。成功完成本拨款申请中提出的工作将确定PVR预防或早期治疗的最佳策略。重要的是，这项工作还将确定动物模型中的眼部安全性概况，以便进行必要的临床前研究，以考虑未来在人类疾病中的临床试验。这项工作的重要影响将是确定潜在的治疗策略，通过在视网膜脱离或穿孔性眼损伤的初始修复时进行治疗，或作为治疗已建立的PVR的辅助剂来预防PVR。预计成功完成这项拨款申请中提出的研究将成为科学证据的基础，可以迅速导致人类疾病的临床试验。临床试验超出了本报告的范围，可能会导致新的治疗方法，并导致恢复视力或预防穿透性眼外伤或视网膜脱离后的失明。这项工作有潜力推进研究领域，并最终改变受影响个体的护理标准，并与通过跨学科研究改善医疗保健的战略目标保持一致。

DESCRIPTION (provided by applicant): Proliferative vitreoretinopathy (PVR) occurs after retinal detachment and severe ocular trauma and leads to both pre-retinal and subretinal scar formation, one of the major determinants of poor outcomes for these patients. Importantly, PVR may be found in greater than 50% of patients with perforating injuries and in up to 10% of retinal detachment patients. Although the pathophysiology of PVR is not completely understood, current evidence implicates various cell types including the retinal pigment epithelium (RPE) in an aberrant wound healing response. The long term objectives of this work is to develop a new strategy to effectively prevent or treat this response in order to decrease the risk of blindness or permanent loss of vision from PVR. The health relatedness of this proposal is that successful completion of this work could lead to preservation of vision in affected individuals. Recent studies support the hypothesis that control EMP2 (epithelial membrane protein 2), or its downstream signaling pathway, may change the biologic response of RPE cells and prevent or treat PVR. The specific aims proposed in this grant submission will test the hypothesis that downregulation of EMP2 or its signal transduction pathway could be effective in prevention or therapy of PVR both in vitro and in an in vivo animal model of disease. Three different approaches will be used in the animal models including an inhibitor that is used currently in cancer therapy, a designer antibody developed in our laboratory, and a small molecule inhibitor of a biochemical pathway. Successful completion of the work proposed in this grant submission will identify the optimum strategy for prevention or early therapy for PVR. Importantly this work will also define the ocular safety profile in an animal model in order to perform the preclinical studies necessary to contemplate future clinical trials in human disease. The significant impact of this work will be to identify potential therapeutic strategies for prevention of PVR through treatment at the time of initial repair of retinal detachment or perforating ocular injury or as an adjunctive agent in treatment of established PVR. It is anticipated that successful completion of the studies proposed in this grant application would form the basis of the scientific evidence that could quickly lead to clinical trials in human disease. The clinical trials, beyond the scope of the present submission, could potentially lead to new therapies and result in restoration of sight or prevention of blindness following penetrating ocular trauma or retinal detachment. This work has potential to both advance the field of research and to ultimately change the standard of care for affected individuals and is aligned with the strategic goals of improving healthcare through interdisciplinary research. PUBLIC HEALTH RELEVANCE: The purpose of this study is to test whether new observations made in our laboratories could be used in order to design a novel therapeutic approach for proliferative virteoretinopathy (PVR), a potentially blinding disease that is associated with severe eye trauma or retinal detachments. Epithelial membrane protein 2 (EMP2), a protein that is normally found in the eye and may be linked to development of PVR, will be targeted for decreased function using a designer antibody fragment or a small molecule inhibitor. The relevance to public health would be to use the observations that result from this study and develop a new therapy that will either prevent or effectively treat PVR.