Susceptibility to autoimmune heart disease depends not only on self-reactive lymphocytes but also on genetically determined target organ sensitivity to autoantibodies.
Indicates genetically determined cardiac sensitivity to autoantibodies in mouse myocarditis; leaves open human translation and therapeutic targeting.
Injury to cardiac myocytes often leads to the production of anti-myosin antibodies. While these antibodies are a marker of myocardial injury, their contribution to pathogenesis in diseases such as autoimmune myocarditis or rheumatic fever is much less clear. We demonstrate in this report that monoclonal anti-myosin antibodies can mediate myocarditis in a susceptible mouse strain. Additionally, we show disease susceptibility depends on the presence of myosin or a myosin-like molecule in cardiac extracellular matrix. This study demonstrates that susceptibility to autoimmune heart disease depends not only on the activation of self-reactive lymphocytes but also on genetically determined target organ sensitivity to autoantibodies.
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Liao et al. (1995) studied this question.
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