Department of Rheumatology, St James' Hospital, Ushers Quay, Dublin D08 NHY1, Ireland.
Royal National Hospital for Rheumatic Diseases, Royal United Hospitals, Combe Park, Bath BA1 3NG, UK.
Rheum Dis Clin North Am. 2020 May;46(2):357-365. doi: 10.1016/j.rdc.2020.01.014.
Axial spondyloathritis (axSpA) treatment with biologic DMARDs was previously focused around anti-TNF agents. Significant advances in research have led to new therapeutic options, such as secukinumab, an IL-17 inhibitor, which has been approved for the treatment of axSpA. Two other biologic agents that are already licensed for rheumatoid and psoriatic arthritis, tofacitinib and ixekizumab, have demonstrated improved outcomes in axSpA. Several newer agents have been developed to inhibit IL-17, IL-23, and JAK. Early trials are promising; however, further research is needed. Rapid expansion of therapies available to treat axSpA could lead to improved disease control and decreased disease burden.
生物 DMARDs 治疗中轴型脊柱关节炎(axSpA)以前主要集中在抗 TNF 药物上。研究的重大进展带来了新的治疗选择,如 IL-17 抑制剂司库奇尤单抗,已被批准用于 axSpA 的治疗。另外两种已批准用于类风湿关节炎和银屑病关节炎的生物制剂,托法替布和依奇珠单抗,在 axSpA 中也显示出了更好的疗效。还有几种新型药物被开发出来以抑制 IL-17、IL-23 和 JAK。早期试验结果很有前景,但仍需要进一步的研究。可用于治疗 axSpA 的治疗方法的快速扩展可能会改善疾病控制并降低疾病负担。