Department of Microbiology&Immunology, Yong Loo Lin School of Medicine, Immunology program, Life Sciences Institute, National University of Singapore, Singapore, Singapore.
Expert Opin Drug Discov. 2020 Mar;15(3):359-371. doi: 10.1080/17460441.2019.1659241. Epub 2019 Aug 30.
: Hand, foot and mouth disease (HFMD) is a serious public health concern in the Asia-Pacific region with recurrent cyclical outbreaks. Enterovirus 71 (EV-A71) and coxsackievirus type A are the main causative agents of HFMD. While majority of HFMD cases are mild and self-limiting, neurological complications have been reported for EV-A71 associated HFMD. There is currently no effective treatment against HFMD and monovalent vaccines against EV-A71 are currently limited to the Chinese market.: As of today, HFMD antiviral development has focused on EV-A71 and involves conventional screening of drug libraries. In recent years, attention has shifted toward identifying druggable host factors to avoid drug resistance and identify drug candidates with broader antiviral activity across EV-A71 genogroups and other HFMD causative agents.: The effective development of HFMD interventions requires us to address the gaps in our understanding of its pathogenesis at the molecular level. The limited resources devoted to the development of HFMD treatment strategies worldwide also contribute to the slow progress of promising drug and vaccine candidates along the clinical pipeline.
手足口病(HFMD)是亚太地区严重的公共卫生问题,经常出现周期性爆发。肠道病毒 71 型(EV-A71)和柯萨奇病毒 A 是手足口病的主要病原体。虽然大多数手足口病病例为轻症自限性疾病,但 EV-A71 相关手足口病可出现神经系统并发症。目前尚无针对手足口病的有效治疗方法,单价疫苗针对 EV-A71 目前仅局限于中国市场。
截至目前,手足口病抗病毒药物研发主要集中在 EV-A71 上,涉及对药物库的常规筛选。近年来,人们的注意力逐渐转向确定可药物治疗的宿主因子,以避免耐药性,并确定具有更广泛抗 EV-A71 各基因群和其他手足口病病原体活性的候选药物。
有效开发手足口病干预措施需要我们解决在分子水平上对手足口病发病机制理解的不足。全球用于开发手足口病治疗策略的资源有限,这也导致有前景的药物和疫苗候选物沿着临床研发管线进展缓慢。