TY - JOUR
T1 - Coxsackievirus-induced myocarditis
T2 - New trends in treatment
AU - Liu, Zhen
AU - Yuan, Ji
AU - Yanagawa, Bobby
AU - Qiu, Dexin
AU - McManus, Bruce M.
AU - Yang, Decheng
N1 - Funding Information:
The authors thank the Heart and Stroke Foundation of British Columbia and Yukon and the Canadian Institutes of Health Research for grant-in-aid support (DC Yang and B McManus) and studentships (J Yuan).
PY - 2005/8
Y1 - 2005/8
N2 - Myocarditis is a common inflammatory heart disease in children and young adults that may result in chronically dilated cardiomyopathy. Coxsacklevirus B3 is the major etiologic agent of this disease. Current treatments for patients with viral myocarditis are almost entirely supportive. In recent years, some promising therapeutic candidates have emerged, including novel treatments and improvements of existing drugs. Among these are molecules that specially target virus entry, such as pleconaril, WIN 54954 and CAR-Fc; nucleic acid-based antiviral agents that inhibit viral translation and/or transcription, such as antisense oligodeoxynucleotide and short interfering RNA; and immunomodulatory agents that augment the host-protective immune responses to effectively clear viruses from target tissues, including interferons and immunoglobulins. In addition, certain new antiviral strategies, still in the early stages, include modulation of signal transduction pathways responsible for viral replication using enzyme inhibitors, which have revealed potential therapeutic targets for viral myocarditis. Finally, the progress in cellular cardiomyoplasty for end-stage therapy, in particular the preliminary clinical trials, is also discussed with respect to its potential future application.
AB - Myocarditis is a common inflammatory heart disease in children and young adults that may result in chronically dilated cardiomyopathy. Coxsacklevirus B3 is the major etiologic agent of this disease. Current treatments for patients with viral myocarditis are almost entirely supportive. In recent years, some promising therapeutic candidates have emerged, including novel treatments and improvements of existing drugs. Among these are molecules that specially target virus entry, such as pleconaril, WIN 54954 and CAR-Fc; nucleic acid-based antiviral agents that inhibit viral translation and/or transcription, such as antisense oligodeoxynucleotide and short interfering RNA; and immunomodulatory agents that augment the host-protective immune responses to effectively clear viruses from target tissues, including interferons and immunoglobulins. In addition, certain new antiviral strategies, still in the early stages, include modulation of signal transduction pathways responsible for viral replication using enzyme inhibitors, which have revealed potential therapeutic targets for viral myocarditis. Finally, the progress in cellular cardiomyoplasty for end-stage therapy, in particular the preliminary clinical trials, is also discussed with respect to its potential future application.
KW - Antisense oligodeoxynucleotide
KW - Cellular cardiomyoplasty
KW - Coxsackievirus B3
KW - Interferon
KW - Pleconaril
KW - Signal intervention
KW - Small interfering RNA
KW - Viral myocarditis
KW - WIN compound
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UR - http://www.scopus.com/inward/citedby.url?scp=24044506253&partnerID=8YFLogxK
U2 - 10.1586/14787210.3.4.641
DO - 10.1586/14787210.3.4.641
M3 - Review article
C2 - 16107202
AN - SCOPUS:24044506253
SN - 1478-7210
VL - 3
SP - 641
EP - 650
JO - Expert Review of Anti-Infective Therapy
JF - Expert Review of Anti-Infective Therapy
IS - 4
ER -