Rahajamanana Vonintsoa L, Thériault Mathieu, Rabezanahary Henintsoa, Sahnoun Yesmine G, Mallet Maria Christina, Isabel Sandra, Trottier Sylvie, Baz Mariana
Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du CHU de Québec-Université Laval, Quebec City, QC G1V 0E8, Canada.
Centre de Recherche en Infectiologie, Université Laval, Quebec City, QC G1V 0E8, Canada.
Infect Dis Rep. 2025 Jun 1;17(3):61. doi: 10.3390/idr17030061.
BACKGROUND/OBJECTIVES: Enterovirus-D68 (EV-D68) and rhinoviruses are major contributors to respiratory illnesses in children, presenting a spectrum of clinical manifestations ranging from asymptomatic cases to severe lower respiratory tract infections. No specific antiviral treatments are currently approved for these viruses.
We conducted a comprehensive literature review of antiviral agents investigated for EV-D68 and rhinovirus infections.
Several antiviral candidates are under investigation, each targeting distinct stages of the viral replicative cycle. Capsid-binding agents and monoclonal antibodies prevent viral attachment by blocking receptor-virus interactions. Inhibitors of viral replication proteins disrupt polyprotein processing and replication organelle biogenesis by targeting non-structural viral proteins. Host factor inhibitors impair viral attachment, replication organelle formation, or RNA replication by interfering with critical host pathways.
While no specific antivirals are yet approved for EV-D68 and rhinovirus infections, emerging therapeutic candidates offer potential avenues for treatment. Continued preclinical and clinical investigation will be essential to validate these approaches and expand the available options for affected patients.
背景/目的:肠道病毒D68型(EV-D68)和鼻病毒是导致儿童呼吸道疾病的主要病原体,临床表现多样,从无症状感染到严重的下呼吸道感染。目前尚无针对这些病毒的特异性抗病毒治疗方法获批。
我们对针对EV-D68和鼻病毒感染所研究的抗病毒药物进行了全面的文献综述。
有几种抗病毒候选药物正在研究中,每种药物针对病毒复制周期的不同阶段。衣壳结合剂和单克隆抗体通过阻断受体-病毒相互作用来防止病毒附着。病毒复制蛋白抑制剂通过靶向病毒非结构蛋白来破坏多蛋白加工和复制细胞器的生物发生。宿主因子抑制剂通过干扰关键的宿主途径来损害病毒附着、复制细胞器形成或RNA复制。
虽然目前尚无针对EV-D68和鼻病毒感染的特异性抗病毒药物获批,但新出现的治疗候选药物为治疗提供了潜在途径。持续的临床前和临床研究对于验证这些方法并为受影响患者扩大可用选择至关重要。