Department of Immunology & Pathology, Monash University, Level 6, The Alfred, Commercial Road, Melbourne 3181, VIC, Australia.
Gynae-oncology Unit, Royal Women's Hospital, 20 Flemington Road, Parkville, Melbourne, Victoria 3052, Australia.
Curr Med Chem. 2018;25(36):4785-4806. doi: 10.2174/0929867324666170712160621.
Interleukin 6 (IL-6), a well-known pro-inflammatory cytokine with pleiotropic activity is a central player in chronic inflammatory diseases including cancers. Therefore, blockade of the IL-6 signalling pathway has become a target for the therapy of diverse cancers such as multicentric Castleman's disease (CD), multiple myeloma and solid tumours including renal, prostate, lung, colorectal and ovarian cancers. Monoclonal antibodies against IL-6 (Siltuximab) and the IL-6 receptor (IL-6R) (Tocilizumab) have emerged as potential immunotherapies, alone or in combination with conventional chemotherapy. Human trials have demonstrated the ability to block IL-6 activity and in multicentric CD lead to durable clinical response and longer disease stabilisation. However, the efficacy of these treatments is still debatable for other cancers. New generation therapeutics in development such as Clazakizumab, Sarilumab, and soluble gp130-Fc have the additional features of improved binding affinity, better specificity with reduced adverse effects. A deeper understanding of the immunological basis of these agents, as well as of the challenges that are faced by immunotherapy-based products in clinical trials, will help select the most promising anti-IL-6/IL-6R therapies for large scale use. Concurrently, current research efforts to personalize treatments may help in the treatment of patients that would greatly benefit from IL-6 blocking therapies.
白细胞介素 6(IL-6)是一种具有多种活性的熟知的促炎细胞因子,是包括癌症在内的慢性炎症性疾病的主要参与者。因此,阻断 IL-6 信号通路已成为治疗多种癌症的靶点,如多发性骨髓瘤、多种中心性 Castleman 病(CD)和实体瘤,包括肾、前列腺、肺、结直肠和卵巢癌。针对 IL-6(西妥昔单抗)和 IL-6 受体(IL-6R)(托珠单抗)的单克隆抗体已成为潜在的免疫疗法,单独或与常规化疗联合使用。人体试验已经证明了阻断 IL-6 活性的能力,并且在多发性骨髓瘤 CD 中导致持久的临床反应和更长的疾病稳定。然而,这些治疗方法在其他癌症中的疗效仍存在争议。新一代治疗药物,如 Clazakizumab、Sarilumab 和可溶性 gp130-Fc,具有改善的结合亲和力、更好的特异性和减少的不良反应等额外特征。更深入地了解这些药物的免疫学基础,以及免疫疗法产品在临床试验中面临的挑战,将有助于为大规模使用选择最有前途的抗 IL-6/IL-6R 治疗方法。同时,目前针对个性化治疗的研究努力可能有助于治疗那些将从 IL-6 阻断治疗中受益最大的患者。