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Immune checkpoint inhibitor-associated myocarditis: manifestations arms mechanisms

期刊

JOURNAL OF CLINICAL INVESTIGATION
卷 131, 期 5, 页码 -

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI145186

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资金

  1. NIH [R01HL141466, R01HL131862, P01AI56299, P01AI039671, R01H130861, R01HL138475]
  2. US Department of Defense [C180476P1, PR191593]
  3. American Heart Association [18SRG34280018]
  4. Foundation Leducq [RA15CVD04]

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Immune checkpoint inhibitors have revolutionized the treatment of cancer, but associated toxicities like myocarditis pose challenges that require further research, predictive biomarker identification, and improved diagnostic and treatment strategies.
Immune checkpoint inhibitors (ICIs) have transformed the treatment of various cancers, including malignancies once considered untreatable. These agents, however, are associated with inflammation and tissue damage in multiple organs. Myocarditis has emerged as a serious ICI-associated toxicity, because, while seemingly infrequent, it is often fulminant and lethal. The underlying basis of 10-associated myocarditis is not completely understood. While the importance of T cells is clear, the inciting antigens, why they are recognized, and the mechanisms leading to cardiac cell injury remain poorly characterized. These issues underscore the need for basic and clinical studies to define pathogenesis, identify predictive biomarkers, improve diagnostic strategies, and develop effective treatments. An improved understanding of ICI-associated myocarditis will provide insights into the equilibrium between the immune and cardiovascular systems.

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