异柠檬酸脱氢酶
胶质瘤
免疫疗法
免疫系统
肿瘤微环境
癌症研究
IDH1
生物
突变体
免疫学
酶
基因
遗传学
生物化学
作者
Dongming Yan,Weicheng Li,Qibing Liu,Kun Yang
标识
DOI:10.3389/fimmu.2022.914618
摘要
The tumor immune microenvironment and immunotherapy have become current important tumor research concerns. The unique immune microenvironment plays a crucial role in the malignant progression of isocitrate dehydrogenase (IDH) mutant gliomas. IDH mutations in glioma can inhibit tumor-associated immune system evasion of NK cell immune surveillance. Meanwhile, mutant IDH can inhibit classical and alternative complement pathways and directly inhibit T-cell responses by metabolizing isocitrate to D-2-Hydroxyglutaric acid (2-HG). IDH has shown clinically relevant efficacy as a potential target for immunotherapy. This article intends to summarize the research progress in the immunosuppressive microenvironment and immunotherapy of IDH-mutant glioma in recent years in an attempt to provide new ideas for the study of occurrence, progression, and treatment of IDH-mutant glioma.
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