Antigen selection and off-tumor toxicity |
Using tumor-associated antigens (TAAs) as target antigens in CAR T cell therapy |
[183,185,187] |
Control of CAR T cell therapy associated toxicity, including: iCARs, multivalent CARs, and implementation of suicide genes |
[190,191,192] |
Tumor heterogeneity and antigen loss |
Using armored CAR T cells |
[198] |
Using bystander killing approach |
[197] |
Using drugs, especially epigenetic drugs to up-regulate TAAs |
[202] |
Using multivalent CAR T cells |
[194] |
Insufficient infiltration and penetration |
Using CAR T cells that express corresponding chemokine receptors (Suggestion) |
[210] |
Using engineered CAR T cells expressing heparinase or other enzymes that can degrade ECM components |
[212] |
Immunosuppressive tumor microenvironment |
Using CAR T cells resistant to immunosuppressive molecules including adenosine |
[216,217] |
Using inhibitory receptor knock out/down CAR T cells |
[215] |