Literature DB >> 31215390

Advancement of Mechanisms of Coxsackie Virus B3-Induced Myocarditis Pathogenesis and the Potential Therapeutic Targets.

Tolessa Muleta Daba1,2, Yue Zhao3, Zhenwei Pan3.   

Abstract

Viral myocarditis is a cardiac disease caused by Group B Coxsackie virus of Enterovirus genus in the Picorna viridae family. It causes heart failure in children, young and adults. Ten Percent (10%) of acute heart failure and 12% of sudden deaths in young and adults who are less than 40 years is due to this viral myocarditis. If treatment action is not taken earlier, the viral disease can develop into chronic myocarditis and Dilated Cardiomyopathy which lead to congestive heart failure. And these eventually result in a reduced cardiac function which finally brings the victim to death. The only treatment option of the disease is heart transplantation once the acute stage of disease develops to chronic and Dilated Cardiomyopathy. Currently, there is a limitation in daily clinical treatments and even some available treatment options are ineffective. Therefore, focusing on search for treatment options through investigation is imperative. Recent studies have reported that biological molecules show a promising role. But their mechanism of pathogenesis is still unclear. A detailed study on identifying the role of biological molecules involved in Coxsackie B3 virus induced myocarditis and their mechanisms of pathogenesis; compiling and disseminating the findings of the investigation to the scientific communities contribute one step forward to the solution. Therefore, this review is aimed at compiling information from findings of current studies on the potential therapeutic role of micro RNA, cytokines and chemokines on the mechanism of pathogenesis of Coxsackie virus B3- induced myocarditis to give brief information for scholars to conduct a detailed study in the area. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Entities:  

Keywords:  CVB3; Chemokines; Cytokines; Dilated Cardiomyopathy; Viral myocarditis; micro RNA.

Year:  2019        PMID: 31215390     DOI: 10.2174/1389450120666190618124722

Source DB:  PubMed          Journal:  Curr Drug Targets        ISSN: 1389-4501            Impact factor:   3.465


  3 in total

1.  Long non-coding RNA MEG3 inhibits M2 macrophage polarization by activating TRAF6 via microRNA-223 down-regulation in viral myocarditis.

Authors:  Yu-Long Xue; Sheng-Xiao Zhang; Chao-Feng Zheng; Yu-Feng Li; Li-Hui Zhang; Qin-Yi Su; Yu-Fei Hao; Shu Wang; Xue-Wen Li
Journal:  J Cell Mol Med       Date:  2020-10-13       Impact factor: 5.310

2.  Coxsackievirus B3 Infection of Human iPSC Lines and Derived Primary Germ-Layer Cells Regarding Receptor Expression.

Authors:  Janik Böhnke; Sandra Pinkert; Maria Schmidt; Hans Binder; Nicole Christin Bilz; Matthias Jung; Uta Reibetanz; Antje Beling; Dan Rujescu; Claudia Claus
Journal:  Int J Mol Sci       Date:  2021-01-27       Impact factor: 5.923

3.  Identification of Cardiac CircRNAs in Mice With CVB3-Induced Myocarditis.

Authors:  Xiang Nie; Jiahui Fan; Huihui Li; Jin Wang; Rong Xie; Chen Chen; Dao Wen Wang
Journal:  Front Cell Dev Biol       Date:  2022-02-07
  3 in total

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