Rheumatoid arthritis is a systemic inflammatory disorder that mainly affect
s the diarthrodial joint. It is the most common form of inflammatory arthri
tis, and has a substantial societal effect in terms of cost, disability, an
d lost productivity. Although the pathogenesis of rheumatoid arthritis rema
ins incompletely understood, much insight into the cellular and molecular m
echanisms involved has been gained in the past decade. On the basis of thes
e insights, new therapies have been developed, and clinical trials have sho
wn the efficacy of aggressive treatment of patients with active disease. In
this review, we discuss improvements in our understanding of the pathophys
iology of inflammatory synovitis in rheumatoid arthritis, and improvements
in therapy for patients with the disorder. The past decade has seen substan
tial advances in these areas. Future studies will be directed at improving
methods for early diagnosis and identification of patients with progressive
disease, and at Improving methods to Identify candidates for subclasses of
disease-modifying antirheumatic drugs (DMARDs). Long-term safety and effic
acy data for the new DMARD agents and combination regimens will also furthe
r delineate efficacy and toxicity and thus the appropriate clinical context
for use of these therapeutic approaches. The continuing elucidation of pat
hophysiological pathways relevant in rheumatoid arthritis, coupled with con
tinuing advances In biotechnology and rational drug design, offer substanti
al hope for the continued development of increasingly potent and specific p
harmacotherapy for treatment of rheumatoid arthritis.