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Treating inflammation by blocking interleukin-1 in a broad spectrum of diseases

Journal

NATURE REVIEWS DRUG DISCOVERY
Volume 11, Issue 8, Pages 633-652

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrd3800

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Funding

  1. US National Institutes of Health [AI-15614, AR-45584, CA-04 6934]
  2. VIDI grant from the Netherlands Research Fund

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Interleukin-1 (IL-1) is a highly active pro-inflammatory cytokine that lowers pain thresholds and damages tissues. Monotherapy blocking IL-1 activity in autoinflammatory syndromes results in a rapid and sustained reduction in disease severity, including reversal of inflammation-mediated loss of sight, hearing and organ function. This approach can therefore be effective in treating common conditions such as post-infarction heart failure, and trials targeting a broad spectrum of new indications are underway. So far, three IL-1-targeted agents have been approved: the IL-1 receptor antagonist anakinra, the soluble decoy receptor rilonacept and the neutralizing monoclonal anti-IL-1 beta antibody canakinumab. In addition, a monoclonal antibody directed against the IL-1 receptor and a neutralizing anti-IL-1 alpha antibody are in clinical trials.

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