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纳米材料介导的肿瘤相关巨噬细胞重编程用于抗肿瘤治疗。

Nanomaterials-Involved Tumor-Associated Macrophages' Reprogramming for Antitumor Therapy.

机构信息

State Key Laboratory of Separation Membrane and Membrane Process, School of Chemistry & School of Electronic and Information Engineering, Tiangong University, Tianjin 300387, P. R. China.

School of Materials Science and Engineering & School of Chemical Engineering and Technology, Tiangong University, Tianjin 300387, P. R. China.

出版信息

ACS Nano. 2024 Mar 19;18(11):7769-7795. doi: 10.1021/acsnano.3c12387. Epub 2024 Feb 29.

Abstract

Tumor-associated macrophages (TAMs) play pivotal roles in tumor development. As primary contents of tumor environment (TME), TAMs secrete inflammation-related substances to regulate tumoral occurrence and development. There are two kinds of TAMs: the tumoricidal M1-like TAMs and protumoral M2-like TAMs. Reprogramming TAMs from immunosuppressive M2 to immunocompetent M1 phenotype is considered a feasible way to improve immunotherapeutic efficiency. Notably, nanomaterials show great potential for biomedical fields due to their controllable structures and properties. There are many types of nanomaterials that exhibit great regulatory activities for TAMs' reprogramming. In this review, the recent progress of nanomaterials-involved TAMs' reprogramming is comprehensively discussed. The various nanomaterials for TAMs' reprogramming and the reprogramming strategies are summarized and introduced. Additionally, the challenges and perspectives of TAMs' reprogramming for efficient therapy are discussed, aiming to provide inspiration for TAMs' regulator design and promote the development of TAMs-mediated immunotherapy.

摘要

肿瘤相关巨噬细胞(TAMs)在肿瘤发展中起着关键作用。作为肿瘤微环境(TME)的主要成分,TAMs 分泌炎症相关物质来调节肿瘤的发生和发展。有两种 TAMs:杀伤性 M1 样 TAMs 和促肿瘤性 M2 样 TAMs。将具有免疫抑制作用的 M2 型 TAMs 重编程为具有免疫能力的 M1 表型被认为是提高免疫治疗效率的一种可行方法。值得注意的是,由于其可控的结构和性质,纳米材料在生物医学领域具有巨大的潜力。有许多类型的纳米材料对 TAMs 的重编程表现出巨大的调节活性。本文全面讨论了纳米材料介导的 TAMs 重编程的最新进展。总结并介绍了用于 TAMs 重编程的各种纳米材料和重编程策略。此外,还讨论了 TAMs 重编程用于有效治疗的挑战和前景,旨在为 TAMs 调节剂的设计提供启示,并促进 TAMs 介导的免疫治疗的发展。

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