Advances in Nanotechnology-Based Immunotherapy for Glioblastoma

被引:13
作者
Tang, Lin [1 ,2 ]
Zhang, Ming [3 ]
Liu, Chaoyong [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing, Peoples R China
[2] Beijing Univ Chem Technol, Coll Life Sci & Technol, Beijing, Peoples R China
[3] Peking Univ Int Hosp, Dept Pathol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
immunotherapy; nanotechnology; blood-brain barrier; nanomaterial; glioblastoma; TUMOR-ASSOCIATED MACROPHAGES; IMMUNOGENIC CELL-DEATH; CENTRAL-NERVOUS-SYSTEM; MANNOSYLATED LIPOSOMES; TARGETED DELIVERY; DRUG; POLARIZATION; MICROGLIA;
D O I
10.3389/fimmu.2022.882257
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Glioblastoma (GBM) is the most aggressive type of brain tumor. Despite the multimodal therapies, the effectiveness of traditional treatments is not much satisfying. In recent years, immunotherapy has become the focus of tumor treatment. Unlike traditional treatments that directly target tumor cells, immunotherapy uses the body's immune system to kill tumors. However, due to the severe immunosuppressive microenvironment of GBM, it generally has a poor response to immunotherapy. In addition, the existence of the blood-brain barrier (BBB) also compromises the immunotherapeutic efficacy. Therefore, effective immunotherapy of GBM requires the therapeutic agents to not only efficiently cross the BBB but also relieve the strong immunosuppression of the tumor microenvironment of GBM. In this review, we will first introduce the CNS immune system, immunosuppressive mechanism of GBM, and current GBM immunotherapy strategies. Then, we will discuss the development of nanomaterials for GBM immunotherapy based on different strategies, roughly divided into four parts: immune checkpoint therapy, targeting tumor-associated immune cells, activating immune cells through immunogenic cell death, and combination therapy, to provide new insights for future GBM immunotherapy.
引用
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页数:8
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