1.江西省儿童医院小儿心脏病治疗中心 江西 南昌 330006
2.南昌大学医学部 江西 南昌 330006
3.江西省卫生健康儿童心血管疾病重点实验室 江西 南昌 330006
曾向帆,女,1998—,医学硕士生,主要从事心肌炎的相关基础与临床研究,E⁃mail:2519880673@qq.com
黄纪毅,男,1991—,医学硕士,助理研究员,主要从事心肌炎的相关基础与临床研究,E⁃mail:jxsetyyhjy@163.com
收稿:2023-10-25,
纸质出版:2025-07-25
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曾向帆,黄纪毅,段君凯.儿童病毒性心肌炎常见病毒受体结构及进入机制研究进展[J].武汉大学学报(医学版),2025,46(07):949-954.
ZENG Xiangfan,HUANG Jiyi,DUAN Junkai.Progress in the study of the structure and entry mechanism of the common viral receptor for viral myocarditis in children[J].Medical Journal of Wuhan University,2025,46(07):949-954.
曾向帆,黄纪毅,段君凯.儿童病毒性心肌炎常见病毒受体结构及进入机制研究进展[J].武汉大学学报(医学版),2025,46(07):949-954. DOI: 10.14188/j.1671-8852.2023.0566.
ZENG Xiangfan,HUANG Jiyi,DUAN Junkai.Progress in the study of the structure and entry mechanism of the common viral receptor for viral myocarditis in children[J].Medical Journal of Wuhan University,2025,46(07):949-954. DOI: 10.14188/j.1671-8852.2023.0566.
病毒性心肌炎(VMC)是病毒侵犯心肌所致局限性或弥漫性的炎症,目前该病尚无特异性治疗手段。已知30多种病毒易导致VMC,如柯萨奇B组病毒、疱疹病毒、新型冠状病毒及流感病毒等,这些病毒通过血管内皮或心肌细胞表面受体感染机体,造成心脏不同程度受累。柯萨奇B组病毒是VMC最常见的病原体,由心肌细胞表面高度表达的柯萨奇⁃腺病毒受体介导入胞,损伤心肌细胞并激活免疫反应。研究显示,阻碍病毒与受体结合或下调受体表达能直接减少机体感染。近年来,随着病毒与受体结合机制的深入研究,发现了许多新的治疗靶点,本文主要对VMC的常见病毒受体结构及其进入机制研究进展进行综述,旨在为设计抗病毒候选药物和亚单位疫苗提供基础。
Viral myocarditis (VMC) is a limited or diffuse inflammation caused by viral invasion of the myocardium
and there is no specific treatment for this disease. More than 30 viruses are known to cause VMC
such as Coxsackie group B viruses
herpesviruses
SARS⁃CoV⁃2
and influenza viruses etc. These viruses infect the body through the endothelium of the blood vessels or the surface receptors of the cardiac myocytes
resulting in varying degrees of cardiac involvement. Coxsackie group B virus
the most common pathogen of VMC
is mediated into the cell by the coxsackie⁃adenovirus receptor
which is highly expressed on the surface of cardiomyocytes
to damage cardiomyocytes and activate immune responses. Studies have shown that impeding viral binding to the receptor or downregulating receptor expression directly reduces infection in the body. In recent years
many new therapeutic targets have been discovered with the development of in⁃depth studies on the mechanisms of virus⁃receptor binding. This article focuses on a review of the progress in the study of the structure of common viral receptors and their entry mechanisms in VMCs to provide a basis for the design of antiviral drug candidates and subunit vaccines.
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