Qi Zhiqing, Maher John
King's College London, Department of Precision and Population Oncology, School of Cancer and Pharmaceutical Sciences, Guy's Hospital, London, UK.
Department of Immunology, Eastbourne Hospital, Eastbourne, East Sussex, UK.
Transl Cancer Res. 2026 Jan 31;15(1):67. doi: 10.21037/tcr-2025-1806. Epub 2026 Jan 27.
Interleukin-12 (IL-12) is a pleiotropic pro-inflammatory cytokine with potent antitumour activity and has been extensively explored as a candidate for cancer immunotherapy. However, its clinical development has been severely limited by the substantial systemic toxicities observed following systemic administration of recombinant IL-12. Nevertheless, the capacity of IL-12 to remodel the immunosuppressive tumour microenvironment (TME) by enhancing immune effector cell activation, proliferation, and infiltration, as well as by shifting suppressive immune cells toward a proinflammatory phenotype, underscores the need to engineer safe delivery strategies that confine cytokine activity to the tumour site. Herein, this review provides a broad and updated overview of diverse strategies for targeted IL-12 delivery to tumours. Specifically, we focus on immunocytokines, adoptive T-cell therapies, and biodegradable polymeric microspheres, while also briefly touching on protein-engineering and nanotechnology-based approaches. By reviewing their modes of action and comparing their benefits and challenges, we illustrate how modern engineering approaches have the potential to overcome the historical barriers to IL-12 therapy while preserving its potent and pleiotropic antitumour functions. Although numerous IL-12-based platforms have recently emerged, an integrative framework that connects advances across diverse engineering modalities has been lacking. Finally, we consider how combination strategies incorporating multiple therapeutic components may enable the safe deployment of IL-12 while fully realising its antitumour potential.
白细胞介素-12(IL-12)是一种具有多种功能的促炎细胞因子,具有强大的抗肿瘤活性,已被广泛探索作为癌症免疫治疗的候选药物。然而,重组IL-12全身给药后观察到的严重全身毒性严重限制了其临床开发。尽管如此,IL-12通过增强免疫效应细胞的激活、增殖和浸润,以及将抑制性免疫细胞转变为促炎表型来重塑免疫抑制性肿瘤微环境(TME)的能力,凸显了设计将细胞因子活性限制在肿瘤部位的安全递送策略的必要性。在此,本综述提供了针对肿瘤靶向递送IL-12的多种策略的广泛且最新的概述。具体而言,我们重点关注免疫细胞因子、过继性T细胞疗法和可生物降解的聚合物微球,同时也简要提及基于蛋白质工程和纳米技术的方法。通过回顾它们的作用方式并比较它们的优点和挑战,我们说明了现代工程方法如何有潜力克服IL-12治疗的历史障碍,同时保留其强大且多效的抗肿瘤功能。尽管最近出现了许多基于IL-12的平台,但缺乏一个连接不同工程模式进展的综合框架。最后,我们考虑结合多种治疗成分的联合策略如何能够在充分实现其抗肿瘤潜力的同时安全地部署IL-12。