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Using the Past to Inform the Future: Anti-VEGF Therapy as a Road Map to Develop Novel Therapies for Diabetic Retinopathy

机译:用过去指导未来:抗VEGF治疗是发展糖尿病性视网膜病变新疗法的路线图

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摘要

Therapies targeting vascular endothelial growth factor (VEGF) are revolutionizing the treatment of diabetic retinopathy (DR) and diabetic macular edema (DME). In August 2012, ranibizumab, a monoclonal antibody fragment targeting VEGF designed for ocular use, became the first and only U.S. Food and Drug Administration-approved medical therapy for DME and the first approved treatment in over 25 years. This approval was based on strong preclinical data followed by numerous clinical trials that demonstrate an essential role of VEGF in vascular permeability and angiogenesis in both normal physiology and disease pathology. In this Perspective, we will examine the experimental studies and scientific data that aided in the success of the development of therapies targeting VEGF and consider how these approaches may inform the development of future therapeutics for diabetic eye disease. A multipoint model is proposed, based on well-established drug development principles, with the goal of improving the success of clinical drug development. This model suggests that to provide a validated preclinical target, investigators should demonstrate the following: the role of the target in normal physiology, a causal link to disease pathogene-sis, correlation to human disease, and the ability to elicit clinically relevant improvements of disease phenotypes in animal models with multiple, chemically diverse interventions. This model will provide a framework to validate the current preclinical targets and identify novel targets to improve drug development success for DR.
机译:靶向血管内皮生长因子(VEGF)的疗法正在彻底改变糖尿病性视网膜病变(DR)和糖尿病性黄斑水肿(DME)的治疗。 2012年8月,兰尼单抗(一种针对眼部设计的靶向VEGF的单克隆抗体片段)成为美国食品药品监督管理局批准的DME药物疗法中的第一个也是唯一的方法,也是25年来首个获批的疗法。该批准基于强大的临床前数据,随后进行了众多临床试验,这些试验证明了VEGF在正常生理学和疾病病理学中在血管通透性和血管生成中的重要作用。在此观点中,我们将研究有助于成功开发针对VEGF的疗法的实验研究和科学数据,并考虑这些方法如何为糖尿病性眼病的未来疗法提供信息。基于完善的药物开发原则,提出了一个多点模型,目的是提高临床药物开发的成功率。该模型表明,要提供经过验证的临床前目标,研究者应证明以下内容:目标在正常生理中的作用,与疾病病因的因果关系,与人类疾病的相关性以及引起疾病的临床相关改善的能力具有多种化学干预措施的动物模型中的表型。该模型将提供一个框架,以验证当前的临床前指标并确定新的指标以提高DR药物开发的成功率。

著录项

  • 来源
    《Diabetes》 |2013年第6期|1808-1815|共8页
  • 作者单位

    Department of Cellular and Molecular Physiology, Penn State University College of Medicine, Hershey, Pennsylvania;

    Departments of Ophthalmology and Visual Sciences and Molecular and Integrative Physiology, The University of Michigan, Ann Arbor, Michigan;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:46:25

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