Montepaone Monica, Lubrano Ennio, Carboni Alessia, Spadaro Antonio
Unità Operativa Complessa di Reumatologia, Dipartimento di Medicina Interna e Specialità Mediche, Sapienza Università di Roma, Rome.
Academic Rheumatology Unit, Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
Open Access Rheumatol. 2014 Feb 20;6:7-13. doi: 10.2147/OARRR.S56048. eCollection 2014.
Psoriatic arthritis (PsA) is a chronic inflammatory arthritis and considered to be a less severe condition than rheumatoid arthritis. PsA patients have been treated for a long time with a number of different agents, from non-steroidal anti-inflammatory drugs to one or more disease-modifying antirheumatic drugs. In the last decade, recognition of the central role of tumor necrosis factor-alpha (TNFα) in the immunopathogenesis of many rheumatic diseases, including PsA, has led to the development of TNFα blockers. In PsA, these agents are uniquely efficacious in the treatment of different patterns of the disease, as well as slowing progression of erosive damage in the peripheral joints. However, a significant number of patients withdraw from therapy because of failure or poor tolerability. Among the novel therapeutic targets, interleukin (IL)-23/IL-12 has been investigated for the treatment of chronic inflammatory disease. In particular, ustekinumab is a human monoclonal antibody that prevents human IL-12 and IL-23 from binding to the IL-12Rβ1 receptor chain of IL-12 (IL-12Rβ1/β2) and IL-23 (IL-12Rβ1/23R) receptor complexes on the surface of natural killer cells and T-cells. Ustekinumab has been approved only for treatment of chronic plaque psoriasis, but also represents an interesting agent for treatment of PsA.
银屑病关节炎(PsA)是一种慢性炎症性关节炎,被认为是一种比类风湿性关节炎病情较轻的病症。PsA患者长期以来一直使用多种不同药物进行治疗,从非甾体类抗炎药到一种或多种改善病情的抗风湿药物。在过去十年中,认识到肿瘤坏死因子-α(TNFα)在包括PsA在内的许多风湿性疾病的免疫发病机制中的核心作用,导致了TNFα阻滞剂的开发。在PsA中,这些药物在治疗该疾病的不同模式以及减缓外周关节侵蚀性损伤的进展方面具有独特的疗效。然而,相当数量的患者因治疗失败或耐受性差而退出治疗。在新的治疗靶点中,白细胞介素(IL)-23/IL-12已被研究用于治疗慢性炎症性疾病。特别是,优特克单抗是一种人单克隆抗体,可阻止人IL-12和IL-23与自然杀伤细胞和T细胞表面的IL-12(IL-12Rβ1/β2)和IL-23(IL-12Rβ1/23R)受体复合物的IL-12Rβ1受体链结合。优特克单抗仅被批准用于治疗慢性斑块状银屑病,但它也是一种治疗PsA的有趣药物。