Since 1999, the treatment of juvenile idiopathic arthritis (JIA) has been extended with a new category of drugs: biologic agents (also known as biologicals or biologic disease modifying anti-rheumatic drugs). Biologic agents consist of natural proteins, like antibodies and cytokines, and have been developed to target one or more steps of the immune response. Elucidation of many of the cellular and molecular mechanisms of the immune system involved in inflammatory arthritis has resulted in an increasing development of different biologic agents and, in the future, this number will expand even further. Tumour necrosis factor (TNF) is a proinflammatory cytokine that plays a central role in the pathogenesis of juvenile idiopathic arthritis. In systemic disease, interleukin (IL)-1 (a proinflammatory cytokine synthesised by fibroblasts in the synovium and macrophages) and IL-6 (concentrations of which correlate with fever, disease activity, and platelet counts) are also thought to be important. If inhibition of these cytokines is not sufficient, other drugs that aim at T cell blockade and B cell depletion are available. Only etanercept (TNF-alpha receptor antagonist), adalimumab (anti-TNF-alpha antibody), abatacept (selective T-cell co-stimulation modulator) and tocilizumab (IL-6 receptor antibody) have been approved by the European Medicines Agency and the Food and Drug Administration for the treatment of JIA. Until now, also infliximab (anti-TNF-alpha antibody), anakinra (IL-1 receptor antagonist), canakinumab (anti-IL-1 antibody) and rilonacept (IL-1 receptor antagonist), though not approved, are available options or under investigation for the treatment of JIA. All of the above mentioned agents have been studied in randomized controlled clinical trials with inclusion of JIA patients.But after approval and sometimes off-label use in daily clinical practice, prospective observational studies are crucial to evaluate the longterm effectiveness and safety in a non-selected patient group. Furthermore, additional ...