CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Therapeutic application of IL-12 for cancer therapy.
Therapeutic application of IL-12 for cancer therapy.
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白细胞介素-12(IL-12)是一种具有强效抗肿瘤活性的多效性促炎细胞因子,已被广泛探索为癌症免疫治疗的候选药物。然而,由于全身给予重组IL-12后观察到显著的全身毒性,其临床开发受到严重限制。尽管如此,IL-12通过增强免疫效应细胞的活化、增殖和浸润,以及将抑制性免疫细胞向促炎表型转变,从而重塑免疫抑制性肿瘤微环境(TME)的能力,凸显了设计安全递送策略以将细胞因子活性局限于肿瘤部位的必要性。本文综述了靶向IL-12递送至肿瘤的多种策略的广泛且最新的概述。
具体而言,我们聚焦于免疫细胞因子、过继性T细胞疗法和可生物降解聚合物微球,同时也简要涉及蛋白质工程和基于纳米技术的策略。通过回顾其作用方式并比较其优势与挑战,我们阐明了现代工程方法如何有潜力克服IL-12治疗的历史性障碍,同时保留其强效且多效的抗肿瘤功能。尽管近期涌现了大量基于IL-12的平台,但一个连接不同工程模式进展的整合性框架一直缺失。
最后,我们探讨了包含多种治疗组分的联合策略如何能够在安全部署IL-12的同时充分实现其抗肿瘤潜力。
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.
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