嵌合抗原受体
癌症研究
肿瘤细胞
实体瘤
渗透(HVAC)
肿瘤微环境
内皮
医学
免疫疗法
免疫学
免疫系统
癌症
材料科学
内科学
复合材料
作者
Parvin Akbari,Afroditi Katsarou,Roxanna Daghighian,Lotte W.H.G. van Mil,Elisabeth J. M. Huijbers,Arjan W. Griffioen,Judy R. van Beijnum
标识
DOI:10.1016/j.bbcan.2022.188701
摘要
For successful application of chimeric antigen receptor (CAR) T cell therapy in solid tumors, major hurdles have to be overcome. CAR T cells have to cross the vascular barrier, which is hampered by the anergic state of the tumor vasculature, characterized by suppressed levels of leukocyte adhesion molecules on the endothelium. Additional immunosuppressive mechanisms in the solid tumor microenvironment can affect infiltration, activity and persistence of CAR T cells. Redirecting CAR T cells towards the tumor vasculature poses a possible solution, as molecular targets of tumor endothelial cells can be directly engaged from within the blood. In this review, we discuss recent advances in CAR T cell therapy against solid tumors, with a focus on targeting the tumor vasculature. Furthermore, we discuss opportunities to overcome challenges and barriers through engineering of CAR T cells to enhance trafficking, safety and efficacy.
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