Diebold Becky A, Smith Susan M E, Li Yang, Lambeth J David
1 Department of Pathology and Laboratory Medicine, Emory University School of Medicine , Atlanta, Georgia.
2 Department of Biology and Physics, Kennesaw State University , Kennesaw, Georgia.
Antioxid Redox Signal. 2015 Aug 10;23(5):375-405. doi: 10.1089/ars.2014.5862. Epub 2014 Mar 24.
NOX2 is important for host defense, and yet is implicated in a large number of diseases in which inflammation plays a role in pathogenesis. These include acute and chronic lung inflammatory diseases, stroke, traumatic brain injury, and neurodegenerative diseases, including Alzheimer's and Parkinson's Diseases.
Recent drug development programs have targeted several NOX isoforms that are implicated in a variety of diseases. The focus has been primarily on NOX4 and NOX1 rather than on NOX2, due, in part, to concerns about possible immunosuppressive side effects. Nevertheless, NOX2 clearly contributes to the pathogenesis of many inflammatory diseases, and its inhibition is predicted to provide a novel therapeutic approach.
Possible side effects that might arise from targeting NOX2 are discussed, including the possibility that such inhibition will contribute to increased infections and/or autoimmune disorders. The state of the field with regard to existing NOX2 inhibitors and targeted development of novel inhibitors is also summarized.
NOX2 inhibitors show particular promise for the treatment of inflammatory diseases, both acute and chronic. Theoretical side effects include pro-inflammatory and autoimmune complications and should be considered in any therapeutic program, but in our opinion, available data do not indicate that they are sufficiently likely to eliminate NOX2 as a drug target, particularly when weighed against the seriousness of many NOX2-related indications. Model studies demonstrating efficacy with minimal side effects are needed to encourage future development of NOX2 inhibitors as therapeutic agents.
NOX2对宿主防御至关重要,但却与大量炎症在发病机制中起作用的疾病有关。这些疾病包括急慢性肺部炎症性疾病、中风、创伤性脑损伤以及神经退行性疾病,如阿尔茨海默病和帕金森病。
近期的药物研发项目针对了多种与各种疾病相关的NOX亚型。部分由于对可能的免疫抑制副作用的担忧,重点主要放在了NOX4和NOX1上,而非NOX2。然而,NOX2显然在许多炎症性疾病的发病机制中起作用,预计对其抑制将提供一种新的治疗方法。
讨论了靶向NOX2可能产生的副作用,包括这种抑制可能导致感染增加和/或自身免疫性疾病的可能性。还总结了现有NOX2抑制剂的领域现状以及新型抑制剂的靶向开发情况。
NOX2抑制剂在治疗急慢性炎症性疾病方面显示出特别的前景。理论上的副作用包括促炎和自身免疫并发症,在任何治疗方案中都应予以考虑,但我们认为,现有数据并未表明它们足以使NOX2不能成为药物靶点,特别是与许多与NOX2相关的适应症的严重性相比时。需要进行模型研究以证明疗效且副作用最小,以鼓励未来将NOX2抑制剂开发为治疗药物。