CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunometabolism, a new therapeutic development for immunotherapies of high-grade gliomas: a narrative review.
Immunometabolism, a new therapeutic development for immunotherapies of high-grade gliomas: a narrative review.
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这里所呈现的免疫代谢研究的意义,应在未来高级别胶质瘤的研究和免疫治疗开发中加以考虑,以最大程度提高患者生存率。
免疫治疗已显著改善多种癌症类型的生存率,但其对胶质母细胞瘤(GBM)的影响相对有限。人们越来越关注理解癌症代谢的作用及其在肿瘤生长和治疗反应中的作用。因此,同样重要的是考虑免疫细胞代谢对癌症进展的临床意义以及对治疗开发的影响。我们的目标是介绍与高级别胶质瘤免疫治疗开发相关的免疫代谢研究新进展。
进行了文献检索和综述,涉及研究高级别胶质瘤中免疫细胞代谢通路的原创研究文章。检索于2022年5月15日和6月13日在PubMed和Embase数据库中进行。选择英文原创研究文章,并根据其是否包含与胶质瘤肿瘤微环境中髓系和淋系细胞代谢变化相关的研究结果进行优先排序。关键内容与发现:高级别胶质瘤(如GBM)中的免疫细胞通过免疫抑制和高治疗耐药性促进肿瘤生长和持续存在,涉及许多代谢机制。代谢优化也已通过多种方式被证明可改善已在临床试验中或已投入使用的免疫疗法,包括树突状细胞疫苗和CAR-T 细胞。
Immunotherapy has yielded significant improvements in survival for many cancer types, but its impact on glioblastoma (GBM) has been relatively muted. There is a growing interest in understanding the role of cancer metabolism and its role in tumor growth and therapeutic response. Thus, it is equally important to consider the clinical implications of immune cell metabolism on cancer progression and implications for therapeutic development. Our objective is to present new developments in immunometabolic research that are relevant to immunotherapy development for high-grade gliomas.
A literature search and review was conducted, regarding original research articles studying metabolic pathways of immune cells in high-grade gliomas. Searches were conducted in PubMed and Embase databases on May 15 and June 13, 2022. English-language original research articles were selected and prioritized based on their inclusion of findings related to metabolic changes in myeloid and lymphoid cells in the glioma tumor microenvironment. KEY CONTENT AND FINDINGS: There are many metabolic mechanisms by which immune cells in high-grade gliomas, like GBM, contribute to tumor growth and persistence via immunosuppression and high therapeutic resistance. There are also several ways that metabolic optimization has already been shown to improve immunotherapies already in clinical trials or in use, including dendritic cell vaccines and chimeric antigen receptor T cells.
The implications of immunometabolic research presented here should be taken into consideration in future research and immunotherapy development of high-grade gliomas for our best chances at improving patient survival.
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