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mRNA 递送在肿瘤免疫治疗中的应用

英文原题:Applications of mRNA Delivery in Cancer Immunotherapy.

PubMed 2025/03/17(内容时间) Int J Nanomedicine Q1 · IF 8.7(JCR 2025)

研究概要

癌症治疗不断进步,免疫治疗作为一种标准模式日益突出,已显著改善多种恶性肿瘤的治疗。

中文摘要

癌症治疗持续进步,免疫治疗日益成为标准治疗方式,并显著改善了多种恶性肿瘤的管理。尽管取得这些进展,免疫治疗疗效仍不一致:某些癌症应答有限,不同患者的结局也存在显著差异。因此,提高免疫治疗疗效至关重要。一个有前景的方向是 mRNA 递送:使用脂质体、肽纳米颗粒、无机纳米颗粒和外泌体等载体,将编码肿瘤抗原、免疫刺激或免疫调节分子的 mRNA 载荷递送至肿瘤免疫微环境(TIME),以激活免疫系统并靶向清除肿瘤细胞。本综述介绍这些载体的特征与局限,并总结目前常见 mRNA 载荷在肿瘤治疗中的应用和机制。此外,考虑到免疫检查点抑制剂(ICI)和嵌合抗原受体(CAR)细胞疗法已在包括黑色素瘤、非小细胞肺癌、头颈部鳞状细胞癌、三阴性乳腺癌、胃癌在内的实体瘤以及白血病中实现重要临床应用,并成为一线治疗,本文重点讨论 mRNA 递送与 ICI、CAR-T、CAR-NK 及 CAR-巨噬细胞疗法联合的最新进展。联合策略可增强 ICI 和 CAR 细胞疗法的靶向能力及疗效,同时减少传统方法相关的长期脱靶毒性。最后,本文分析当前 mRNA 递送系统的局限,例如核酸酶导致的 mRNA 不稳定、免疫原性风险、载体制备复杂,以及剂量和安全性方面的知识缺口。解决这些挑战对于释放 mRNA 在癌症免疫治疗中的潜力至关重要。总体而言,探索 mRNA 递送可加深对癌症免疫治疗的理解,并有望开发个体化、有效的治疗策略,增强癌症患者免疫应答并延长生存时间。

展开英文摘要原文

Cancer treatment is continually advancing, with immunotherapy gaining prominence as a standard modality that has markedly improved the management of various malignancies. Despite these advancements, the efficacy of immunotherapy remains variable, with certain cancers exhibiting limited response and patient outcomes differing considerably. Thus, enhancing the effectiveness of immunotherapy is imperative. A promising avenue is mRNA delivery, employing carriers such as liposomes, peptide nanoparticles, inorganic nanoparticles, and exosomes to introduce mRNA cargos encoding tumor antigens, immune-stimulatory, or immune-modulatory molecules into the tumor immune microenvironment (TIME). This method aims to activate the immune system to target and eradicate tumor cells. In this review, we introduce the characteristics and limitations of these carriers and summarize the application and mechanisms of currently prevalent cargos in mRNA-based tumor treatment. Additionally, given the significant clinical application of immune checkpoint inhibitors (ICIs) and chimeric antigen receptor (CAR)-based cell therapies in solid tumors (including melanoma, non-small-cell lung cancer, head and neck squamous cell carcinoma, triple-negative breast cancer, gastric cancer) and leukemia, which have become first-line treatments, we highlight and discuss recent progress in combining mRNA delivery with ICIs, CAR-T, CAR-NK, and CAR-macrophage therapies. This combination enhances the targeting capabilities and efficacy of ICIs and CAR-cell-based therapies, while also mitigating the long-term off-target toxicities associated with conventional methods. Finally, we analyze the limitations of current mRNA delivery systems, such as nuclease-induced mRNA instability, immunogenicity risks, complex carrier production, and knowledge gaps concerning dosing and safety. Addressing these challenges is crucial for unlocking the potential of mRNA in cancer immunotherapy. Overall, exploring mRNA delivery enriches our comprehension of cancer immunotherapy and holds promise for developing personalized and effective treatment strategies, potentially enhancing the immune responses of cancer patients and extending their survival time.

论文信息

作者
Pan X、Zhang YW、Dai C、Zhang J、Zhang M、Chen X
单位
Department of Hepatobiliary & Pancreatic Surgery, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.China
文献类型
综述
期刊
International journal of nanomedicine2025
原文标识
PubMed 40125430 · DOI 10.2147/IJN.S500520