Division of Rheumatology and Clinical Immunology, Humanitas Clinical and Research Center - IRCCS, Rozzano (Mi), Italy.
Department of Biomedical Sciences, Humanitas University, Rozzano (Mi), Italy.
Front Immunol. 2021 Jun 2;12:622770. doi: 10.3389/fimmu.2021.622770. eCollection 2021.
The term spondyloarthritis (SpA) encompasses a heterogeneous group of inflammatory musculoskeletal diseases with several common genetic background and clinical features, including the possible involvement of the axial skeleton with peripheral mono- or oligo- arthritis and frequently coexisting skin, eye and intestinal manifestations. When the sacroiliac joints or other parts of the spine or thoracic wall are predominantly affected at magnetic resonance or X-ray imaging with inflammatory back pain, the disease is classified as axial SpA and the therapeutic choices are significantly different compared to cases of peripheral arthritis. Moving from the narrow effectiveness and safety profiles of non-steroidal anti-inflammatory drugs, there has been a significant research effort aimed at identifying new treatments based on our better understanding of the pathogenesis of SpA. Indeed, in parallel with the solid data demonstrating that IL-17 and IL-23 are key cytokines in the development of enthesitis and spondylitis, monoclonal antibodies interfering with this pathway have been developed for the treatment of axial SpA. Furthermore, the IL-17/IL-23 axis is key to extra-articular manifestations such as inflammatory bowel disease, uveitis, and psoriasis which are frequent comorbidities of SpA. Currently available drugs act through these mechanisms recognizing IL-23 and targeting IL-17, such as secukinumab and ixekizumab. These therapeutic approaches are now envisioned in the international treatment recommendations for psoriatic arthritis with an axial phenotype as well as for ankylosing spondylitis (AS). We will provide herein a concise comprehensive overview of the clinical evidence supporting the use of these and other drugs acting on IL-23 and IL-17 in axial SpA.
术语脊柱关节炎(SpA)包含一组具有多种共同遗传背景和临床特征的异质性炎症性肌肉骨骼疾病,包括可能涉及轴骨骼和外周单关节炎或寡关节炎,并经常伴有皮肤、眼睛和肠道表现。当骶髂关节或脊柱或胸壁的其他部位在磁共振成像或 X 射线成像中主要受累,伴有炎症性背痛时,该疾病被归类为轴性 SpA,与外周关节炎相比,治疗选择有显著差异。从非甾体抗炎药的狭窄有效性和安全性特征出发,已经进行了大量研究工作,旨在根据我们对 SpA 发病机制的更好理解来确定新的治疗方法。事实上,随着证明 IL-17 和 IL-23 是附着点炎和脊柱炎发展的关键细胞因子的可靠数据的出现,针对该途径的单克隆抗体已被开发用于治疗轴性 SpA。此外,IL-17/IL-23 轴是关节外表现(如炎症性肠病、葡萄膜炎和银屑病)的关键,这些表现是 SpA 的常见合并症。目前可用的药物通过这些机制作用,识别 IL-23 并靶向 IL-17,例如司库奇尤单抗和依奇珠单抗。这些治疗方法现在被认为是治疗具有轴性表型的银屑病关节炎和强直性脊柱炎(AS)的国际治疗建议的一部分。我们将在此提供对这些和其他作用于 IL-23 和 IL-17 的药物在轴性 SpA 中应用的临床证据的简明综合概述。