Immune mechanisms of group B coxsackievirus induced viral myocarditis

被引:27
作者
Zhang, Yue [1 ,2 ]
Zhou, Xiaobin [1 ]
Chen, Shuyi [1 ]
Sun, Xinchen [1 ]
Zhou, Chenglin [1 ]
机构
[1] Nanjing Med Univ, Affiliated Taizhou Peoples Hosp, Clin Med Lab Ctr, Taizhou, Peoples R China
[2] Nantong Univ, Sch publ Hlth, Nantong, Peoples R China
关键词
Viral myocarditis; innate immunity; adaptive immunity; pattern recognition receptors (PRRs); T lymphocytes; DILATED CARDIOMYOPATHY; PARVOVIRUS B19; NLRP3; INFLAMMASOME; RECEPTOR; INNATE; CELLS; INFECTION; CONTRIBUTES; ACTIVATION; EXPRESSION;
D O I
10.1080/21505594.2023.2180951
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Viral myocarditis is known to be a primary cause of dilated cardiomyopathy (DCM) that can lead to heart failure and sudden cardiac death and is invariably caused by myocardial viral infection following active inflammatory destruction of the myocardium. Although acute viral myocarditis frequently recovers on its own, current chronic myocarditis therapies are unsatisfactory, where the persistence of viral or immunological insults to the heart may play a role. Cellular and mouse experimental models that utilized the most prevalent Coxsackievirus group B type 3 (CVB3) virus infection causing myocarditis have illustrated the pathophysiology of viral myocarditis. In this review, immunological insights into the different stages of development of viral myocarditis were discussed, concentrating on the mechanisms of innate and adaptive immunity in the development of CVB3-induced myocarditis.
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页数:11
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