A Novel Application for a Rheumatologic Medication
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causing fatigue, anemia, inflammation and damage to bones, cartilage and tissue.Abstract
Rheumatology has enjoyed significant advances in pharmacotherapy over the past two decades. Now, with our arsenals buffered, we ask, “Can these novel anti-rheumatic drugs escape the niche of rheumatology? Is their utility beyond the joints and autoimmunological processes? Say perhaps, myocardial infarctions?”Enter tocilizumab (Actemra®). Tocilizumab is a novel humanized monoclonal anti-body approved by the US Food and Drug Administration in 2010 for the treatment of rheu-matoid arthritis and (later) juvenile idiopathic arthritis. The drug is administered as either a monthly intravenous infusion or as a weekly (or every other week) subcutaneous injection. The dose of the monthly infusion can vary between 4 mg/kg and 8 mg/kg but the once a week or every other week injection is 162 mg subcutaneously. In patients with rheumatoid arthritis, interleukin 6 (IL-6) is overproduced in the body, causing fatigue, anemia, inflammation and damage to bones, cartilage and tissue. Acting as an antagonist of IL-6 receptors, tocilizumab in-terferes with the pro-inflammatory effects of the IL-6–IL-6 receptor interaction. This response can be objectively gauged with serum C-Reactive Protein (CRP), offering a clinically practical and quantitative measure of inflammation.
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