Insights into the mechanisms of apoptosis and pathogenesis in enterovirus 71 infections: A review

医学 上睑下垂 坏死性下垂 肠道病毒71 疾病 细胞凋亡 肠道病毒 免疫学 临床试验 重症监护医学 生物信息学 程序性细胞死亡 炎症体 病理 病毒 炎症 生物 生物化学
作者
Jiamei Wu,Cheng-Si Wang,Xi-wen Yu
出处
期刊:Medicine [Wolters Kluwer]
卷期号:104 (15): e42183-e42183
标识
DOI:10.1097/md.0000000000042183
摘要

This study examines the intricate interactions between enterovirus 71 (EV71) and various programmed cell death pathways, specifically apoptosis, necroptosis, and pyroptosis, which collectively shape the pathogenesis and severity of EV71 infections. Primarily affecting children under 5 years of age, EV71 is a leading cause of hand, foot, and mouth disease and has been linked to severe neurological and systemic complications. This paper highlights how EV71 leverages distinct cell death mechanisms to enhance viral replication and amplify disease pathology. Apoptosis, for example, may restrict viral dissemination by systematically eliminating infected cells; however, EV71’s activation of necroptosis and pyroptosis induces robust inflammatory responses, potentially resulting in extensive tissue damage and adverse health outcomes. Additionally, this study also summarizes recent advancements in the field, with an emphasis on experimental studies and clinical trials focused on vaccine and antiviral therapy development. Despite substantial progress, challenges persist, notably in achieving reliable vaccine efficacy and formulating safe treatment options specifically for pediatric populations. Moving forward, the review suggests that future research should delve further into understanding EV71-related complications, developing broad-spectrum antiviral agents, and investigating host genetic factors that may influence disease progression and outcomes. Ultimately, this research is essential for the development of targeted interventions capable of reducing severe symptoms without compromising the immune response, underscoring the importance of these efforts for public health and the management of infectious diseases.
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