CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Mesoporous Silica Nanoparticles as an Ideal Platform for Cancer Immunotherapy: Recent Advances and Future Directions.
Mesoporous Silica Nanoparticles as an Ideal Platform for Cancer Immunotherapy: Recent Advances and Future Directions.
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癌症免疫治疗最近改变了针对各种癌症恶性肿瘤的传统方法。免疫治疗包括全身和局部治疗,以增强针对癌症的免疫反应,并涉及免疫检查点、癌症疫苗、免疫调节剂、模拟抗原呈递细胞和过继细胞治疗等策略。尽管结果令人鼓舞,但这些方法仍然存在若干局限性,包括缺乏将免疫调节剂精准递送至靶细胞以及脱靶毒性等,而这些问题可以通过纳米技术克服。介孔二氧化硅纳米颗粒(MSNs)因其有利的结构特征而被研究用于改善癌症免疫治疗的各个方面。MSNs可以被工程化改造以改变其性质,如大小、形状、孔隙率、表面功能性和佐剂性。本综述探讨了MSNs的免疫学特性,以及MSNs作为免疫佐剂、疫苗和模拟抗原呈递细胞(APCs)递送载体的应用。本综述还详细介绍了当前重塑肿瘤微环境以使其正向响应抗肿瘤免疫细胞的策略,以及MSNs用于免疫治疗并与其他抗肿瘤疗法(包括光动力/热疗法)联合以增强抗癌治疗效果的应用。最后,讨论了MSNs用于癌症免疫治疗的当前需求和未来前景。
Cancer immunotherapy recently transforms the traditional approaches against various cancer malignancies. Immunotherapy includes systemic and local treatments to enhance immune responses against cancer and involves strategies such as immune checkpoints, cancer vaccines, immune modulatory agents, mimetic antigen-presenting cells, and adoptive cell therapy. Despite promising results, these approaches still suffer from several limitations including lack of precise delivery of immune-modulatory agents to the target cells and off-target toxicity, among others, that can be overcome using nanotechnology. Mesoporous silica nanoparticles (MSNs) are investigated to improve various aspects of cancer immunotherapy attributed to the advantageous structural features of this nanomaterial.
MSNs can be engineered to alter their properties such as size, shape, porosity, surface functionality, and adjuvanticity. This review explores the immunological properties of MSNs and the use of MSNs as delivery vehicles for immune-adjuvants, vaccines, and mimetic antigen-presenting cells (APCs).
The review also details the current strategies to remodel the tumor microenvironment to positively reciprocate toward the anti-tumor immune cells and the use of MSNs for immunotherapy in combination with other anti-tumor therapies including photodynamic/thermal therapies to enhance the therapeutic effect against cancer. Last, the present demands and future scenarios for the use of MSNs for cancer immunotherapy are discussed.
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