增强癌症免疫疗法:纳米技术介导的免疫疗法克服免疫抑制

IF 14.7 1区 医学 Q1 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Sinica. B Pub Date : 2024-09-01 DOI:10.1016/j.apsb.2024.05.032
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摘要

免疫疗法是一种重要的癌症治疗方法,为治愈癌症患者带来了希望。虽然免疫疗法取得了初步成功,但其广泛应用的一个主要障碍是无法使大多数患者受益。免疫疗法的成败与肿瘤的免疫微环境密切相关。最近,在癌症免疫疗法中,调节肿瘤免疫微环境以激发抗肿瘤免疫反应的策略备受关注。纳米药物的独特物理特性和设计灵活性已被广泛用于靶向免疫细胞(包括肿瘤相关巨噬细胞(TAMs)、T 细胞、髓源抑制细胞(MDSCs)和肿瘤相关成纤维细胞(TAFs)),为癌症免疫疗法带来了希望。在本文中,我们回顾了旨在针对各种免疫细胞调节肿瘤免疫微环境的治疗策略。重点是以纳米药物为基础的癌症免疫疗法模式,目的是诱导或增强抗肿瘤免疫反应,从而改善免疫疗法。值得注意的是,将癌症免疫疗法与化疗、放疗和光动力疗法等其他疗法相结合,可以最大限度地提高治疗效果。最后,我们指出了纳米技术介导的免疫疗法需要克服的挑战,以便设计出更有效的纳米系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Enhancing cancer immunotherapy: Nanotechnology-mediated immunotherapy overcoming immunosuppression

Immunotherapy is an important cancer treatment method that offers hope for curing cancer patients. While immunotherapy has achieved initial success, a major obstacle to its widespread adoption is the inability to benefit the majority of patients. The success or failure of immunotherapy is closely linked to the tumor's immune microenvironment. Recently, there has been significant attention on strategies to regulate the tumor immune microenvironment in order to stimulate anti-tumor immune responses in cancer immunotherapy. The distinctive physical properties and design flexibility of nanomedicines have been extensively utilized to target immune cells (including tumor-associated macrophages (TAMs), T cells, myeloid-derived suppressor cells (MDSCs), and tumor-associated fibroblasts (TAFs)), offering promising advancements in cancer immunotherapy. In this article, we have reviewed treatment strategies aimed at targeting various immune cells to regulate the tumor immune microenvironment. The focus is on cancer immunotherapy models that are based on nanomedicines, with the goal of inducing or enhancing anti-tumor immune responses to improve immunotherapy. It is worth noting that combining cancer immunotherapy with other treatments, such as chemotherapy, radiotherapy, and photodynamic therapy, can maximize the therapeutic effects. Finally, we have identified the challenges that nanotechnology-mediated immunotherapy needs to overcome in order to design more effective nanosystems.

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来源期刊
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
22.40
自引率
5.50%
发文量
1051
审稿时长
19 weeks
期刊介绍: The Journal of the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association oversees the peer review process for Acta Pharmaceutica Sinica. B (APSB). Published monthly in English, APSB is dedicated to disseminating significant original research articles, rapid communications, and high-quality reviews that highlight recent advances across various pharmaceutical sciences domains. These encompass pharmacology, pharmaceutics, medicinal chemistry, natural products, pharmacognosy, pharmaceutical analysis, and pharmacokinetics. A part of the Acta Pharmaceutica Sinica series, established in 1953 and indexed in prominent databases like Chemical Abstracts, Index Medicus, SciFinder Scholar, Biological Abstracts, International Pharmaceutical Abstracts, Cambridge Scientific Abstracts, and Current Bibliography on Science and Technology, APSB is sponsored by the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association. Its production and hosting are facilitated by Elsevier B.V. This collaborative effort ensures APSB's commitment to delivering valuable contributions to the pharmaceutical sciences community.
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