PMID- 17424701 OWN - NLM STAT- MEDLINE DCOM- 20070517 LR - 20151119 IS - 0041-4131 (Print) IS - 0041-4131 (Linking) VI - 85 IP - 1 DP - 2007 Jan TI - [Rheumatoid arthritis: current status of therapy]. PG - 1-8 AB - Rheumatoid Arthritis (RA) is a frequent chronic inflammatory disease characterized by distal, bilateral and symmetrical lesions, leading to joint distortions and articular destructions. RA can also cause severe extra-articular manifestations associated with a poor prognosis. Recent advances in the field of immunopathology of RA have oriented treatment targeting the pro-inflammatory cytokines like tumor necrosis factor-alpha (TNF alpha), interleukin (IL) and IL6. These biotherapies are considered as an important therapeutic progress in the treatment of RA acting at the level of cellular processes responsible for rheumatoid disease. These new therapies are active not only in controlling the disease inflammatory processes but also to stop the radiological course of RA. These new therapies are however efficient as long as prescribed, their interruption being rapidly followed by a flare-up of RA. Multiple adverse events attributed to anti-TNF-alpha have been described especially severe opportunistic infections and tuberculosis. B cells playing a critical role in sustaining the chronic inflammatory process in RA, targeted depleting B cells therapies have been developed in refractory forms of RA giving promising results. However, before any biotherapy prescription especially of anti-TNF-alpha, an initial screening should be achieved to exclude patients with history of untreated tuberculosis, solid cancers, malignant hemopathies or demyelinating disorders. It is also essential to assure a strict follow-up in patients under biotherapy to detect adverse events that can be sometimes severe. Thus, the ratio benefit/risk must be evaluated before any biotherapy prescription. FAU - El Bahri, Dalila Mrabet AU - El Bahri DM AD - Service de Rhumatologie, Hopital La Rabta, Tunis, Tunisie. FAU - Meddeb, Nihel AU - Meddeb N FAU - Sellami, Slaheddine AU - Sellami S LA - fre PT - Comparative Study PT - English Abstract PT - Journal Article PT - Review TT - Actualites therapeutiques de la polyarthrite rhumatoide. PL - Tunisia TA - Tunis Med JT - La Tunisie medicale JID - 0413766 RN - 0 (Adrenal Cortex Hormones) RN - 0 (Anti-Inflammatory Agents) RN - 0 (Anti-Inflammatory Agents, Non-Steroidal) RN - 0 (Antibodies, Monoclonal) RN - 0 (Antibodies, Monoclonal, Humanized) RN - 0 (Antirheumatic Agents) RN - 0 (Immunoglobulin G) RN - 0 (Interleukin 1 Receptor Antagonist Protein) RN - 0 (Interleukin-1) RN - 0 (Receptors, Tumor Necrosis Factor) RN - 0 (Tumor Necrosis Factor-alpha) RN - B72HH48FLU (Infliximab) RN - FYS6T7F842 (Adalimumab) RN - OP401G7OJC (Etanercept) SB - IM MH - Adalimumab MH - Adrenal Cortex Hormones/administration & dosage/therapeutic use MH - Adult MH - Animals MH - Anti-Inflammatory Agents/administration & dosage/adverse effects/therapeutic use MH - Anti-Inflammatory Agents, Non-Steroidal/administration & dosage/adverse effects/therapeutic use MH - Antibodies, Monoclonal/administration & dosage/adverse effects/therapeutic use MH - Antibodies, Monoclonal, Humanized MH - Antirheumatic Agents/administration & dosage/adverse effects/therapeutic use MH - Arthritis, Rheumatoid/complications/drug therapy/physiopathology/*therapy MH - Biological Therapy/adverse effects/methods MH - Controlled Clinical Trials as Topic MH - Disease Models, Animal MH - Etanercept MH - Follow-Up Studies MH - Humans MH - Immunoglobulin G/administration & dosage/adverse effects/therapeutic use MH - Infliximab MH - Interleukin 1 Receptor Antagonist Protein/administration & dosage/adverse effects/therapeutic use MH - Interleukin-1/antagonists & inhibitors MH - Receptors, Tumor Necrosis Factor/administration & dosage/therapeutic use MH - Risk Assessment MH - Spondylarthropathies/drug therapy MH - Tumor Necrosis Factor-alpha/antagonists & inhibitors RF - 66 EDAT- 2007/04/12 09:00 MHDA- 2007/05/18 09:00 CRDT- 2007/04/12 09:00 PHST- 2007/04/12 09:00 [pubmed] PHST- 2007/05/18 09:00 [medline] PHST- 2007/04/12 09:00 [entrez] PST - ppublish SO - Tunis Med. 2007 Jan;85(1):1-8.