PHARMACEUTICAL APPROACHES OF IL-6 INHIBITORS FOR THE TREATMENT OF RHEUMATOID ARTHRITIS, FOCUS ON NEW FDA APPROVED DRUG: SARILUMAB
Reza Andriani* and A. A. Raka Karsana
Abstract
Rheumatoid arthritis (RA) is a chronic inf1ammatory disease of
unknown etiology and the most common form of chronic inflammatory
arthritis and often results in joint damage and physical disability. RA is
characterized by synovial inflammation and hyperplasia, autoantibody
production, cartilage and bone destruction, and systemic features,
including cardiovascular, pulmonary, psychological, and skeletal
disorders. Interleukin-6 (IL-6) is a potent pro-inflammatory agent
which plays a crucial role in the pathogenesis of systemic
inflammatory disease. During acute inflammation in RA, monocytes,
macrophages and endothelial cells release IL-6, accompanied by an
increase in neutrophils in synovial fluids. As disease progresses, IL-6
is thought to influence the shift from acute to chronic inflammation. Recently, the agents
targeting the IL-6 (classes of biologic therapies) and/or its receptor attracted significant
attention as a promising arthritics drug. RA patients with inadequate response to TNF
inhibitor and non-biologic disease modifying anti-rheumatic drugs (DMARDs), demonstrated
a therapeutic response to IL-6 receptor blockers. This article attempts to review the new FDA
approved IL-6 inhibitor drug Sarilumab for RA from pharmaceutical aspects.
Keywords: Sarilumab, Rheumatoid Arthritis, Il-6 inhibitor, IL-6 receptor blockers.
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