Noel R Rose1. 1. Departments of Pathology and of Molecular Microbiology and Immunology, Johns Hopkins Center for Autoimmune Disease Research, Johns Hopkins University, Room 659, Baltimore, MD 21205, USA. nrrose@jhsph.edu
Abstract
INTRODUCTION: Myocarditis, which is the inflammation of the heart muscle, remains a vexing therapeutic problem. Many cases are associated with viral infection, and appropriate treatment may depend upon whether the disease is primarily infectious, immune-mediated, or both. DISCUSSION: The combination of endomyocardial biopsies with newer molecular and immunologic tools holds a promise of distinguishing the different etiologies of myocarditis, thus, guiding future treatments. Nucleic acid hybridization and polymerase chain reaction have been applied to detect viral genome persisting in the heart. Early trials with type 1 interferons have shown a promise inpatients with biopsy-proven enteroviral infection. Antibodies to cardiac antigens and increased HLA expression in cardiac biopsies have been used to identify patients, most likely, to benefit from immunosuppression or immunoadsorption. Future advances in the therapy of inflammatory disease of the heart may be based on detailed studies of myocarditis in animal models. Using coxsackievirus B3 infection or cardiac myosin immunization, we have identified some critical steps leading from a self-limited viral myocarditis to chronic autoimmune myocarditis and sometimes, to dilated cardiomyopathy. CONCLUSION: Myocarditis offers an opportunity to dissect the complex interaction between a viral infection and an autoimmune disease. The lessons learned from investigations in humans and in animal models hold a promise that may lead the way to improved treatments.
INTRODUCTION: Myocarditis, which is the inflammation of the heart muscle, remains a vexing therapeutic problem. Many cases are associated with viral infection, and appropriate treatment may depend upon whether the disease is primarily infectious, immune-mediated, or both. DISCUSSION: The combination of endomyocardial biopsies with newer molecular and immunologic tools holds a promise of distinguishing the different etiologies of myocarditis, thus, guiding future treatments. Nucleic acid hybridization and polymerase chain reaction have been applied to detect viral genome persisting in the heart. Early trials with type 1 interferons have shown a promise inpatients with biopsy-proven enteroviral infection. Antibodies to cardiac antigens and increased HLA expression in cardiac biopsies have been used to identify patients, most likely, to benefit from immunosuppression or immunoadsorption. Future advances in the therapy of inflammatory disease of the heart may be based on detailed studies of myocarditis in animal models. Using coxsackievirus B3 infection or cardiac myosin immunization, we have identified some critical steps leading from a self-limited viral myocarditis to chronic autoimmune myocarditis and sometimes, to dilated cardiomyopathy. CONCLUSION: Myocarditis offers an opportunity to dissect the complex interaction between a viral infection and an autoimmune disease. The lessons learned from investigations in humans and in animal models hold a promise that may lead the way to improved treatments.
Authors: Florian Leuschner; Gabriel Courties; Partha Dutta; Luke J Mortensen; Rostic Gorbatov; Brena Sena; Tatiana I Novobrantseva; Anna Borodovsky; Kevin Fitzgerald; Victor Koteliansky; Yoshiko Iwamoto; Marina Bohlender; Soeren Meyer; Felix Lasitschka; Benjamin Meder; Hugo A Katus; Charles Lin; Peter Libby; Filip K Swirski; Daniel G Anderson; Ralph Weissleder; Matthias Nahrendorf Journal: Eur Heart J Date: 2014-06-20 Impact factor: 29.983
Authors: Ralf J Ludwig; Karen Vanhoorelbeke; Frank Leypoldt; Ziya Kaya; Katja Bieber; Sandra M McLachlan; Lars Komorowski; Jie Luo; Otavio Cabral-Marques; Christoph M Hammers; Jon M Lindstrom; Peter Lamprecht; Andrea Fischer; Gabriela Riemekasten; Claudia Tersteeg; Peter Sondermann; Basil Rapoport; Klaus-Peter Wandinger; Christian Probst; Asmaa El Beidaq; Enno Schmidt; Alan Verkman; Rudolf A Manz; Falk Nimmerjahn Journal: Front Immunol Date: 2017-05-31 Impact factor: 7.561