Katsicas María Martha, Russo Ricardo
Service of Immunology & Rheumatology, Hospital de Pediatría Juan P. Garrahan, Combate de los Pozos 1881, 1245, Buenos Aires, Argentina.
Pediatr Rheumatol Online J. 2016 Mar 12;14(1):17. doi: 10.1186/s12969-016-0076-6.
The juvenile spondyloarthropathies (JSpA) are a group of related rheumatic diseases characterized by involvement of peripheral large joints, axial joints, and entheses (enthesitis) that begin in the early years of life (prior to 16(th) birthday).The nomenclature and concept of spondyloarthropathies has changed during the last few decades. Although there is not any specific classification of JSpA, diseases under the spondyloarthropathy nomenclature umbrella in the younger patients include: the seronegative enthesitis and arthropathy (SEA) syndrome, juvenile ankylosing spondylitis, reactive arthritis, and inflammatory bowel disease-associated arthritis. Moreover, the ILAR criteria for Juvenile Idiopathic Arthritis includes two categories closely related to spondyloarthritis: Enthesitis-related arthritis and psoriatic arthritis.We review the pathophysiology and the use of biological agents in JSpA. JSpA are idiopathic inflammatory diseases driven by an altered balance in the proinflammatory cytokines. There is ample evidence on the role of tumor necrosis factor (TNF) and interleukin-17 in the physiopathology of these entities. Several non-biologic and biologic agents have been used with conflicting results in the treatment of these complex diseases. The efficacy and safety of anti-TNF agents, such as etanercept, infliximab and adalimumab, have been analysed in controlled and uncontrolled trials, usually showing satisfactory outcomes. Other biologic agents, such as abatacept, tocilizumab and rituximab, have been insufficiently studied and their role in the therapy of SpA is uncertain. Interleukin-17-blocking agents are promising alternatives for the treatment of JSpA patients in the near future. Recommendations for the treatment of patients with JSpA have recently been proposed and are discussed in the present review.
青少年脊柱关节炎(JSpA)是一组相关的风湿性疾病,其特征为外周大关节、中轴关节和附着点(附着点炎)受累,发病于早年(16岁生日之前)。在过去几十年中,脊柱关节炎的命名和概念发生了变化。尽管JSpA没有任何特定的分类,但在年轻患者中,属于脊柱关节炎命名范畴的疾病包括:血清阴性附着点炎和关节病(SEA)综合征、青少年强直性脊柱炎、反应性关节炎以及炎症性肠病相关关节炎。此外,青少年特发性关节炎的国际风湿病联盟(ILAR)标准包括与脊柱关节炎密切相关的两类:附着点炎相关关节炎和银屑病关节炎。我们综述了JSpA的病理生理学以及生物制剂的应用。JSpA是由促炎细胞因子平衡改变驱动的特发性炎症性疾病。有充分证据表明肿瘤坏死因子(TNF)和白细胞介素-17在这些疾病的病理生理学中发挥作用。几种非生物制剂和生物制剂在治疗这些复杂疾病时效果不一。抗TNF药物,如依那西普、英夫利昔单抗和阿达木单抗的疗效和安全性已在对照和非对照试验中进行了分析,通常显示出令人满意的结果。其他生物制剂,如阿巴西普、托珠单抗和利妥昔单抗,研究尚不充分,它们在脊柱关节炎治疗中的作用尚不确定。白细胞介素-17阻断剂在不久的将来有望成为治疗JSpA患者的替代药物。最近有人提出了JSpA患者的治疗建议,并在本综述中进行了讨论。