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工程纳米颗粒调控肿瘤微环境中的细胞外基质和免疫组分以用于癌症免疫治疗

英文原题:Engineering Nanoparticles to Modulate Extracellular Matrix and Immune Components of the Tumor Microenvironment in Cancer Immunotherapy.

查看英文原题

Engineering Nanoparticles to Modulate Extracellular Matrix and Immune Components of the Tumor Microenvironment in Cancer Immunotherapy.

PubMed 2025/12/09(内容时间) Biomater Res Q1 · IF 9.8(JCR 2025)

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中文摘要

癌症免疫治疗已成为一种通过利用机体免疫系统治疗恶性肿瘤的变革性策略。然而,其临床疗效往往受到肿瘤微环境(TME)复杂且免疫抑制性质的限制,这对治疗成功构成了重大障碍。TME包含多种组分,包括免疫细胞、癌症相关成纤维细胞、异常血管系统、细胞外基质和可溶性介质,它们共同支持肿瘤进展、抑制免疫监视,并导致治疗耐药和不良预后。纳米技术的最新进展引入了工程化纳米材料,作为调节TME并增强癌症免疫治疗结局的有前景工具。这些纳米材料可被精确设计以与TME的特定元素相互作用,从而实现局部递送、降低全身毒性并提高治疗疗效。本综述全面概述了工程化纳米颗粒在靶向TME细胞组分和非细胞组分中的作用。它重点介绍了纳米载体重编程肿瘤相关免疫细胞(包括T细胞、树突状细胞、NK 细胞和肿瘤相关巨噬细胞)的能力,以及它们靶向癌症相关成纤维细胞、重塑肿瘤血管系统、降解细胞外基质和调节免疫抑制介质的能力。通过探索这些多方面的相互作用,我们阐明了合理设计的纳米材料如何重塑肿瘤格局以恢复免疫功能并增强免疫治疗疗效。

最后,本综述讨论了当前挑战、安全性考量以及将这些创新转化为临床可行疗法所必需的未来方向。

展开英文摘要原文

Cancer immunotherapy has emerged as a transformative strategy for treating malignancies by harnessing the body's immune system.

However, its clinical efficacy is often limited by the complex and immunosuppressive nature of the tumor microenvironment (TME), which poses substantial barriers to therapeutic success. The TME comprises a variety of components, including immune cells, cancer-associated fibroblasts, abnormal vasculature, extracellular matrix, and soluble mediators that collectively support tumor progression, suppress immune surveillance, and contribute to treatment resistance and poor prognosis. Recent advances in nanotechnology have introduced engineered nanomaterials as promising tools to modulate the TME and enhance the outcomes of cancer immunotherapy. These nanomaterials can be precisely engineered to interact with specific elements of the TME, enabling localized delivery, reduced systemic toxicity, and improved therapeutic efficacy.

This review provides a comprehensive overview of the role of engineered nanoparticles in targeting both cellular and noncellular components of the TME. It highlights the capacity of nanocarriers to reprogram tumor-associated immune cells, including T cells, dendritic cells, natural killer cells, and tumor-associated macrophages, as well as their ability to target cancer-associated fibroblasts, remodel tumor vasculature, degrade the extracellular matrix, and modulate immunosuppressive mediators.

By exploring these multifaceted interactions, we illuminate how rationally designed nanomaterials can reshape the tumor landscape to restore immune function and enhance immunotherapeutic efficacy.

Finally, the review addresses current challenges, safety considerations, and future directions necessary to translate these innovations into clinically viable therapies.

论文信息

作者
Dang BT、Pham KY、Nguyen AH、Park J、Kwon TK、Kang JS、Jeong JH、Yook S
第一作者单位
Department of Precision Medicine, School of Medicine, Sungkyunkwan University, Suwon 16419, Republic of Korea.South Korea
通讯作者单位
School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.South Korea
文献类型
综述
期刊
Biomaterials research2025
原文标识
PubMed 41376820 · DOI 10.34133/bmr.0289