Interleukin-18 is a proinflammatory cytokine implicated in acute myocardial infarction and heart failure, with IL-18 binding protein and neutralizing antibodies emerging as potential therapeutic targets.
Acute Myocardial Infarction and Heart Failure
IL-18 binding protein (IL-18BP) and neutralizing IL-18 antibody
Interleukin 18 (IL-18) is a proinflammatory cytokine in the IL-1 family that has been implicated in a number of disease states. In animal models of acute myocardial infarction (AMI), pressure overload, and LPS-induced dysfunction, IL-18 regulates cardiomyocyte hypertrophy and induces cardiac contractile dysfunction and extracellular matrix remodeling. In patients, high IL-18 levels correlate with increased risk of developing cardiovascular disease (CVD) and with a worse prognosis in patients with established CVD. Two strategies have been used to counter the effects of IL-18:IL-18 binding protein (IL-18BP), a naturally occurring protein, and a neutralizing IL-18 antibody. Recombinant human IL-18BP (r-hIL-18BP) has been investigated in animal studies and in phase I/II clinical trials for psoriasis and rheumatoid arthritis. A phase II clinical trial using a humanized monoclonal IL-18 antibody for type 2 diabetes is ongoing. Here we review the literature regarding the role of IL-18 in AMI and heart failure and the evidence and challenges of using IL-18BP and blocking IL-18 antibodies as a therapeutic strategy in patients with heart disease.
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Laura C. O’Brien
Eleonora Mezzaroma
Heart Failure & Transplant
Benjamín W. Van Tassell
Heart Failure & Transplant
Molecular Medicine
Virginia Commonwealth University
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O’Brien et al. (Wed,) conducted a review in Acute Myocardial Infarction and Heart Failure. IL-18 binding protein (IL-18BP) and neutralizing IL-18 antibody was evaluated. Interleukin-18 is a proinflammatory cytokine implicated in acute myocardial infarction and heart failure, with IL-18 binding protein and neutralizing antibodies emerging as potential therapeutic targets.
synapsesocial.com/papers/6a085f2d0df715653be8a8b5 — DOI: https://doi.org/10.2119/molmed.2014.00034