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Given the seminal discovery of the critical and non-redundant immunosuppressive role of A2AR (24) and the therapeutic potential of A2AR blockade for T cellbased immunotherapy (25), our study demonstrates a viable strategy by targeting A2AR in combination with inhibition of lipid peroxidation to improve persistence and functionality of ACT against cancer

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30 Watson JC, Stratakis CA, Bryant-Greenwood PK, et al

B) Bar graph representing the percent correlation of treatment-induced postsynaptic spines to the general presynaptic marker Synapsin

(PDF) Acknowledgments We are grateful to Antonio Velzquez for his generous support and helpful discussions