The interleukin-1 receptor antagonist (IL-1Ra) anakinra is a biologic agent
designed to antagonize the joint destruction, inflammation, and pain assoc
iated with progression of rheumatoid arthritis. Pending FDA approval, anaki
nra will be the first IL-1Ra available to treat rheumatoid arthritis. It wa
s developed to block the proinflammatory effects of interleukin-1, a cytoki
ne present in synovial fluid. A large placebo-controlled trial showed that
anakinra significantly reduces joint destruction over 6 to 12 months, while
an additional study showed significant clinical improvement when anakinra
was added to methotrexate therapy. A transient local injection-site reactio
n is the primary adverse effect. Because anakinra is primarily eliminated r
enally, dosing adjustment may be needed in the elderly and in patients with
renal impairment. Administration is by subcutaneous injection once daily;
the optimal dosage appears to be 75 or 150 mg/day. Anakinra promises to be
another effective treatment option in a disease with no cure.