摘要In a recent publication in Nature,1Mamedov and colleagues identified pathways that modulateγδT cell killing and BTN3A cellular expression through integrating genome-wide CRISPR screens and tumor organoid culture,deepening our comprehen-sion ofγδT cell stress surveillance and proposing novel pathways to boost γδ T cell's anticancer functions(Fig.1).
作者单位Wenzhou Institute,University of Chinese Academy of Sciences,Wenzhou 325000 Zhejiang,China[1]Wenzhou Institute,University of Chinese Academy of Sciences,Wenzhou 325000 Zhejiang,China;School of Physics,Peking University,100871 Beijing,China[2]