工程化益生菌用于肿瘤靶向联合化学免疫治疗
Engineered probiotics for tumor-targeted combination chemoimmunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Lipid-based nanosystems: the next generation of cancer immune therapy.
Lipid-based nanosystems: the next generation of cancer immune therapy.
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免疫疗法已成为肿瘤治疗武器库中的重要组成部分。其在多种癌症类型中的适用性令人瞩目,且利用内源性机制来实现预期目标。然而,脱靶或靶向非肿瘤毒性、活性有限、联合治疗中缺乏控制,以及尤其是对实体瘤而言局部蓄积量低,这些因素共同限制了其临床应用。递送系统部分缓解了这些局限。基于脂质的纳米颗粒(NPs)因其良好的理化特性而成为革命性载体,其特定应用和优势在免疫治疗药物递送中尤为有用。本综述旨在强调免疫治疗所面临的挑战,以及基于脂质的NPs如何已经并可能进一步用于应对这些挑战。
我们讨论了NPs在一系列领域中的近期基础与临床应用,并详细探讨了免疫检查点抑制疗法、过继细胞疗法和细胞因子疗法中的主要障碍。
我们重点阐述了基于脂质的纳米系统如何通过递送、直接调节免疫系统或靶向免疫抑制性肿瘤微环境来应对这些障碍。我们探索了用于核酸递送的先进和新兴脂质体及脂质纳米颗粒(LNP)系统、内在和外在刺激响应型制剂,以及免疫治疗中的仿生基于脂质的纳米系统。
最后,我们讨论脂质基NP免疫疗法临床应用中面临的关键挑战,并提出近期未来的研究方向,以实现这些创新性脂质基纳米系统的潜力,因为它们正成为必要提升免疫疗法疗效的关键垫脚石。
Immunotherapy has become an important part of the oncotherapy arsenal. Its applicability in various cancer types is impressive, as well as its use of endogenous mechanisms to achieve desired ends.
However, off-target or on-target-off-tumor toxicity, limited activity, lack of control in combination treatments and, especially for solid tumors, low local accumulation, have collectively limited clinical use thereof. These limitations are partially alleviated by delivery systems.
Lipid-based nanoparticles (NPs) have emerged as revolutionary carriers due to favorable physicochemical characteristics, with specific applications and strengths particularly useful in immunotherapeutic agent delivery. The aim of this review is to highlight the challenges faced by immunotherapy and how lipid-based NPs have been, and may be further utilized to address such challenges.
We discuss recent fundamental and clinical applications of NPs in a range of areas and provide a detailed discussion of the main obstacles in immune checkpoint inhibition therapies, adoptive cellular therapies, and cytokine therapies.
We highlight how lipid-based nanosystems could address these through either delivery, direct modulation of the immune system, or targeting of the immunosuppressive tumor microenvironment.
We explore advanced and emerging liposomal and lipid nanoparticle (LNP) systems for nucleic acid delivery, intrinsic and extrinsic stimulus-responsive formulations, and biomimetic lipid-based nanosystems in immunotherapy.
Finally, we discuss the key challenges relating to the clinical use of lipid-based NP immunotherapies, suggesting future research directions for the near term to realize the potential of these innovative lipid-based nanosystems, as they become the crucial steppingstone towards the necessary enhancement of the efficacy of immunotherapy.
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