嵌合抗原受体
免疫疗法
肿瘤微环境
癌症研究
医学
细胞疗法
T细胞
癌症免疫疗法
癌症
免疫学
细胞
免疫系统
肿瘤细胞
生物
内科学
遗传学
作者
Yuna Jo,Laraib Amir Ali,Joongpyo Shim,Byung Ha Lee,Changwan Hong
出处
期刊:Cancers
[MDPI AG]
日期:2020-07-28
卷期号:12 (8): 2087-2087
被引量:12
标识
DOI:10.3390/cancers12082087
摘要
Novel engineered T cells containing chimeric antigen receptors (CAR-T cells) that combine the benefits of antigen recognition and T cell response have been developed, and their effect in the anti-tumor immunotherapy of patients with relapsed/refractory leukemia has been dramatic. Thus, CAR-T cell immunotherapy is rapidly emerging as a new therapy. However, it has limitations that prevent consistency in therapeutic effects in solid tumors, which accounts for over 90% of all cancer patients. Here, we review the literature regarding various obstacles to CAR-T cell immunotherapy for solid tumors, including those that cause CAR-T cell dysfunction in the immunosuppressive tumor microenvironment, such as reactive oxygen species, pH, O2, immunosuppressive cells, cytokines, and metabolites, as well as those that impair cell trafficking into the tumor microenvironment. Next-generation CAR-T cell therapy is currently undergoing clinical trials to overcome these challenges. Therefore, novel approaches to address the challenges faced by CAR-T cell immunotherapy in solid tumors are also discussed here.
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