What have we learnt from the inhibition of IL-6 in RA and what are the clinical opportunities for patient outcomes?

IF 3.4 2区 医学 Q2 RHEUMATOLOGY Therapeutic Advances in Musculoskeletal Disease Pub Date : 2024-10-21 eCollection Date: 2024-01-01 DOI:10.1177/1759720X241283340
Peter C Taylor, Eugen Feist, Janet E Pope, Peter Nash, Jean Sibilia, Roberto Caporali, Alejandro Balsa
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Abstract

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.

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我们从抑制 IL-6 在 RA 中的作用中学到了什么?
类风湿性关节炎(RA)是一种自身免疫性疾病,以滑膜关节及其他组织和器官的持续炎症为特征。如不及时治疗,可导致关节损伤、残疾,甚至增加死亡率。这种疾病是由炎性细胞因子引起的,这些细胞因子导致了 RA 中的慢性炎症。白细胞介素-6(IL-6)是一种关键的病理细胞因子,也是旨在缓解局部和全身炎症的治疗目标。尽管人们对RA的认识取得了进展,并引入了新的治疗方法,但实现持续缓解仍具有挑战性。本综述探讨了IL-6在RA发病机制中的作用、其作为治疗靶点的潜力以及个性化医疗在RA管理中的意义。IL-6具有双重信号机制,即经典信号和跨信号,可影响各种细胞内通路。虽然已经出现了几种靶向疗法,但由于疾病的多样性和复杂性,没有一种基于单一机制的疗法是普遍有效的。针对 IL-6 的不同方法已经过测试,包括受体或配体的生物阻断,以及 IL-6 信号的抑制。IL-6受体抑制剂已被证实可作为单独或与其他疗法联合使用的RA疗法。Tocilizumab是首个获批的IL-6抑制剂,它能阻断可溶性和膜结合的IL-6受体,减少炎症级联反应。临床试验证实了托西珠单抗的疗效和安全性,并将其作为对传统疗法无反应患者的一种治疗选择。抑制IL-6的益处不仅在于减轻关节炎症,还能改善贫血、心血管疾病、抑郁症和骨质疏松症等合并症。要想取得最佳疗效,就必须根据患者的情况和并发症量身定制治疗方案。从患者的整体角度出发的 "按特征治疗 "方法可以改善个性化医疗策略。生物仿制药--生物制剂的低成本替代品--进一步提高了治疗的可及性和成本效益。IL-6抑制剂是治疗RA的重要选择,尤其是对有特殊合并症的患者。
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来源期刊
CiteScore
6.80
自引率
4.80%
发文量
132
审稿时长
18 weeks
期刊介绍: Therapeutic Advances in Musculoskeletal Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of musculoskeletal disease.
期刊最新文献
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