Kalam Nida, Balasubramaniam Vinod R M T
Infection and Immunity Research Strength, Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Bandar Sunway, Malaysia.
Influenza Other Respir Viruses. 2024 Dec;18(12):e70064. doi: 10.1111/irv.70064.
Enterovirus-D68 (EV-D68) was first identified in 1962 in pediatric patients with acute respiratory conditions in California, USA (US). From the 1970s to 2005, EV-D68 was underestimated due to limited data and serotyping methods. In 2014, the United States experienced outbreaks of acute flaccid myelitis (AFM) in children EV-D68 positive. WIN-like compounds (pleconaril, pocapavir, and vapendavir) bind to the virus capsid and have been tested against various enteroviruses (EVs) in clinical trials. However, these compounds encountered issues with resistance and adverse effects, which impeded their approval by the Food and Drug Administration (FDA). Presently, the medical field lacks FDA-approved antiviral treatments or vaccines for EV-D68. Ongoing research efforts are dedicated to identifying viable therapeutics to address EV-D68 infections. This review explores the current advancements in antiviral therapies and potential therapeutics to mitigate the significant impact of EV-D68 infection control.
肠道病毒D68型(EV-D68)于1962年在美国加利福尼亚州首次在患有急性呼吸道疾病的儿科患者中被发现。从20世纪70年代到2005年,由于数据和血清分型方法有限,EV-D68一直被低估。2014年,美国儿童中出现了EV-D68阳性的急性弛缓性脊髓炎(AFM)疫情。WIN类化合物(普来可那立、泊卡韦和伐喷达韦)与病毒衣壳结合,并已在临床试验中针对各种肠道病毒(EVs)进行了测试。然而,这些化合物遇到了耐药性和不良反应问题,这阻碍了它们获得美国食品药品监督管理局(FDA)的批准。目前,医学领域缺乏FDA批准的针对EV-D68的抗病毒治疗方法或疫苗。正在进行的研究致力于确定可行的治疗方法来应对EV-D68感染。本综述探讨了抗病毒疗法的当前进展以及减轻EV-D68感染控制重大影响的潜在治疗方法。