Myocarditis: causes, mechanisms, and evolving therapies

被引:10
作者
Kyaw, Tin [1 ,2 ,3 ,8 ]
Drummond, Grant [4 ,5 ]
Bobik, Alex [1 ,2 ,3 ,5 ,6 ]
Peter, Karlheinz [1 ,3 ,4 ,6 ,7 ]
机构
[1] Baker Heart & Diabet Inst, Inflammat & Cardiovasc Dis Lab, Melbourne, Australia
[2] Monash Univ, Monash Med Ctr, Ctr Inflammatory Dis, Melbourne, Australia
[3] Univ Melbourne, Dept Cardiometab Hlth, Melbourne, Australia
[4] La Trobe Univ, Dept Microbiol Anat Physiol & Pharmacol, Melbourne, Australia
[5] La Trobe Univ, Ctr Cardiovasc Biol & Dis Res, Melbourne, Australia
[6] Alfred Hosp, Heart Ctr, Melbourne, Australia
[7] Monash Univ, Dept Immunol, Melbourne, Australia
[8] Baker Heart & Diabet Inst, Commercial Rd, Melbourne, Vic 3004, Australia
关键词
Myocarditis; virus; vaccine; immune checkpoint inhibitors; mRNA vaccines; immunotherapy; HUMAN-HERPESVIRUS; 6; GIANT-CELL MYOCARDITIS; HUMAN CYTOMEGALOVIRUS; NEUTRALIZING ANTIBODY; IMMUNE-RESPONSE; TRANSPLANT RECIPIENTS; ADENOVIRUS RECEPTOR; HEART-FAILURE; VIRUS; EXPRESSION;
D O I
10.1080/14728222.2023.2193330
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionMyocarditis is a severe lymphocyte-mediated inflammatory disorder of the heart, mostly caused by viruses and immune checkpoint inhibitors (ICIs). Recently, myocarditis as a rare adverse event of mRNA vaccines for SARS-CoV-2 has caused global attention. The clinical consequences of myocarditis can be very severe, but specific treatment options are lacking or not yet clinically proven.Areas coveredThis paper offers a brief overview of the biology of viruses that frequently cause myocarditis, focusing on mechanisms important for viral entry and replication following host infection. Current and new potential therapeutic targets/strategies especially for viral myocarditis are reviewed systematically. In particular, the immune system in myocarditis is dissected with respect to infective viral and non-infective, ICI-induced myocarditis.Expert opinionVaccination is an excellent emerging preventative strategy for viral myocarditis, but most vaccines still require further development. Anti-viral treatments that inhibit viral replication need to be considered following viral infection in host myocardium, as lower viral load reduces inflammation severity. Understanding how the immune system continues to damage the heart even after viral clearance will define novel therapeutic targets/strategies. We propose that viral myocarditis can be best treated using a combination of antiviral agents and immunotherapies that control cytotoxic T cell activity.
引用
收藏
页码:225 / 238
页数:14
相关论文
共 165 条
[31]   A bivalent CMV vaccine formulated with human compatible TLR9 agonist CpG1018 elicits potent cellular and humoral immunity in HLA expressing mice [J].
Dasari, Vijayendra ;
Beckett, Kirrilee ;
Horsefield, Shane ;
Ambalathingal, George ;
Khanna, Rajiv .
PLOS PATHOGENS, 2022, 18 (06)
[32]   CARDIAC LOCALIZATION OF EOSINOPHIL-GRANULE MAJOR BASIC-PROTEIN IN ACUTE NECROTIZING MYOCARDITIS [J].
DEMELLO, DE ;
LIAPIS, H ;
JUREIDINI, S ;
NOURI, S ;
KEPHART, GM ;
GLEICH, GJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (22) :1542-1545
[33]   A Series of Patients With Myocarditis Following SARS-CoV-2 Vaccination With mRNA-1279 and BNT162b2 [J].
Dickey, John B. ;
Albert, Elisabeth ;
Badr, Mai ;
Laraja, Kristin M. ;
Sena, Laureen M. ;
Gerson, David S. ;
Saucedo, Jason E. ;
Qureshi, Waqas ;
Aurigemma, Gerard P. .
JACC-CARDIOVASCULAR IMAGING, 2021, 14 (09) :1862-1863
[34]   Structural basis of RNA recognition by the SARS-CoV-2 nucleocapsid phosphoprotein [J].
Dinesh, Dhurvas Chandrasekaran ;
Chalupska, Dominika ;
Silhan, Jan ;
Koutna, Eliska ;
Nencka, Radim ;
Veverka, Vaclav ;
Boura, Evzen .
PLOS PATHOGENS, 2020, 16 (12)
[35]   Eosinophil-derived IL-4 drives progression of myocarditis to inflammatory dilated cardiomyopathy [J].
Diny, Nicola L. ;
Baldeviano, G. Christian ;
Talor, Monica V. ;
Barin, Jobert G. ;
Ong, SuFey ;
Bedja, Djahida ;
Hays, Allison G. ;
Gilotra, Nisha A. ;
Coppens, Isabelle ;
Rose, Noel R. ;
Cihakova, Daniela .
JOURNAL OF EXPERIMENTAL MEDICINE, 2017, 214 (04) :943-957
[36]   Macrophages and cardiac fibroblasts are the main producers of eotaxins and regulate eosinophil trafficking to the heart [J].
Diny, Nicola L. ;
Hou, Xuezhou ;
Barin, Jobert G. ;
Chen, Guobao ;
Talor, Monica V. ;
Schaub, Julie ;
Russell, Stuart D. ;
Klingel, Karin ;
Rose, Noel R. ;
Cihakova, Daniela .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2016, 46 (12) :2749-2760
[37]   Human parvovirus B19NS1 protein modulates inflammatory signaling by activation of STAT3/PIAS3 in human endothelial cells [J].
Duechting, Anja ;
Tschoepe, Carsten ;
Kaiser, Heike ;
Lamkemeyer, Tobias ;
Tanaka, Nobuyuki ;
Aberle, Susanne ;
Lang, Florian ;
Torresi, Joseph ;
Kandolf, Reinhard ;
Bock, C. -Thomas .
JOURNAL OF VIROLOGY, 2008, 82 (16) :7942-7952
[38]   Molecular and Virological Evidence of Viral Activation From Chromosomally Integrated Human Herpesvirus 6A in a Patient With X-Linked Severe Combined Immunodeficiency [J].
Endo, Akifumi ;
Watanabe, Ken ;
Ohye, Tamae ;
Suzuki, Kyoko ;
Matsubara, Tomoyo ;
Shimizu, Norio ;
Kurahashi, Hiroki ;
Yoshikawa, Tetsushi ;
Katano, Harutaka ;
Inoue, Naoki ;
Imai, Kohsuke ;
Takagi, Masatoshi ;
Morio, Tomohiro ;
Mizutani, Shuki .
CLINICAL INFECTIOUS DISEASES, 2014, 59 (04) :545-548
[39]   Chromosomal Integration by Human Herpesviruses 6A and 6B [J].
Flamand, Louis .
HUMAN HERPESVIRUSES, 2018, 1045 :209-226
[40]   Cytomegalovirus Latency and Reactivation: An Intricate Interplay With the Host Immune Response [J].
Forte, Eleonora ;
Zhang Zheng ;
Thorp, Edward B. ;
Hummel, Mary .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2020, 10