嵌合抗原受体
肿瘤微环境
癌症研究
医学
抗原
免疫学
免疫疗法
肿瘤细胞
免疫系统
作者
Hamid Reza Mirzaei,Jamshid Hadjati
出处
期刊:OncoImmunology
[Landes Bioscience]
日期:2015-10-29
卷期号:5 (3): e1100792-e1100792
被引量:4
标识
DOI:10.1080/2162402x.2015.1100792
摘要
To date, chimeric antigen receptor (CAR) T cells have shown remarkable responses in patients with certain hematological malignancies particularly acute lymphocytic leukemia (ALL), but have led to more limited success with solid tumors probably due to immunosuppressive networks in the tumor environment. To overcome this issue, Koneru et al. have recently demonstrated IL-12-producing CAR T cells, also known as armored CAR T cells, to simultaneously target both ovarian tumor cells and their microenvironment. This commentary challenges the study design of Koneru et al. study and highlights the importance of choosing the most appropriate experimental animal model in preclinical cancer studies.
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