Finally, in a highly significant paper in 2018 this group obtained evidence that tumor-reactive CD8(+) T cells can be liberated from tumor-induced immunosuppression by A2AR antagonists and by A2AR but not A2BR gene deletion ( 18 ).
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Can Allosteric Receptor-Protein Interactions in Receptor Complexes Be a Molecular Mechanism Involved in Cancer Immune Therapy?
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