Taylor Peter C, Feist Eugen, Pope Janet E, Nash Peter, Sibilia Jean, Caporali Roberto, Balsa Alejandro
Botnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Windmill Road, Oxford OX3 7LD, UK.
Department of Rheumatology, Helios Clinic Vogelsang-Gommern, Cooperation Partner of the Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
Ther Adv Musculoskelet Dis. 2024 Oct 21;16:1759720X241283340. doi: 10.1177/1759720X241283340. eCollection 2024.
Rheumatoid arthritis (RA) is an autoimmune disease characterised by persistent inflammation of the synovial joints as well as other tissues and organs. Left untreated, it can lead to joint damage, disability and even increased mortality. The disease is driven by inflammatory cytokines that contribute to the chronic inflammation seen in RA. Interleukin-6 (IL-6) is a key pathological cytokine and a target for treatments aiming to alleviate local and systemic inflammation. Despite advances in understanding RA and the introduction of new treatments, achieving sustained remission remains challenging. This review explores the role of IL-6 in RA pathogenesis, its potential as a treatment target and the significance of personalised medicine in RA management. IL-6 has a dual signalling mechanism, classical and trans-signalling, which influences various intracellular pathways. While several targeted therapies have emerged, no single mechanism-based therapy is universally effective due to the diversity and complexity of the disease. Different approaches to targeting IL-6 have been tested, including biologic blockade of receptors or ligands, and inhibition of IL-6 signalling. IL-6 receptor inhibitors have been validated as RA therapeutics, either alone or in combination with other treatments. Tocilizumab, the first approved IL-6 inhibitor, blocks both soluble and membrane-bound IL-6 receptors, reducing the inflammatory cascade. Clinical trials confirm the efficacy and safety of tocilizumab and its role as a treatment option for patients unresponsive to conventional therapies. The benefits of IL-6 inhibition extend beyond reduced joint inflammation to the amelioration of comorbidities like anaemia, cardiovascular disease, depression and osteoporosis. Tailoring treatment to patients' profiles and comorbidities is essential for optimal outcomes. A 'treat-to-profile' approach, focusing on a holistic view of the patient, could improve personalised medicine strategies. Biosimilars - lower-cost alternatives to biologics - further enhance the accessibility and cost-effectiveness of treatment. IL-6 inhibitors present a valuable treatment option for RA management, particularly for patients with specific comorbidities.
类风湿性关节炎(RA)是一种自身免疫性疾病,其特征是滑膜关节以及其他组织和器官持续发炎。若不治疗,它会导致关节损伤、残疾甚至死亡率增加。该疾病由炎症细胞因子驱动,这些细胞因子导致了类风湿性关节炎中出现的慢性炎症。白细胞介素-6(IL-6)是一种关键的病理细胞因子,也是旨在减轻局部和全身炎症的治疗靶点。尽管在理解类风湿性关节炎和引入新治疗方法方面取得了进展,但实现持续缓解仍然具有挑战性。本综述探讨了IL-6在类风湿性关节炎发病机制中的作用、其作为治疗靶点的潜力以及个性化医学在类风湿性关节炎管理中的意义。IL-6具有经典和转信号两种双重信号传导机制,影响各种细胞内途径。虽然已经出现了几种靶向治疗方法,但由于疾病的多样性和复杂性,没有一种基于单一机制的治疗方法是普遍有效的。已经测试了针对IL-6的不同方法,包括受体或配体的生物阻断以及IL-6信号传导的抑制。IL-6受体抑制剂已被验证为类风湿性关节炎的治疗药物,可单独使用或与其他治疗方法联合使用。托珠单抗是首个获批的IL-6抑制剂,可阻断可溶性和膜结合的IL-6受体,减少炎症级联反应。临床试验证实了托珠单抗的疗效和安全性及其作为对传统疗法无反应患者的治疗选择的作用。IL-6抑制的益处不仅限于减轻关节炎症,还包括改善贫血、心血管疾病、抑郁症和骨质疏松症等合并症。根据患者的病情和合并症调整治疗方案对于获得最佳治疗效果至关重要。一种“根据病情治疗”的方法,注重患者的整体情况,可以改善个性化医学策略。生物类似药——生物制品的低成本替代品——进一步提高了治疗的可及性和成本效益。IL-6抑制剂为类风湿性关节炎的管理提供了一种有价值的治疗选择,特别是对于患有特定合并症的患者。