机译:来自HCV感染患者的肝内Vγ9Vδ2T细胞显示出耗尽的表型,但可以抑制HCV复制
IRCCS L Spallanzani INMI Lab Cellular Immunol &
Pharmacol Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Lab Cellular Immunol &
Pharmacol Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Lab Cellular Immunol &
Pharmacol Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Clin Dept Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Clin Dept Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Clin Dept Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Lab Cellular Immunol &
Pharmacol Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Virol Lab Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Clin Dept Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Virol Lab Via Portuense 292 I-00149 Rome Italy;
IRCCS L Spallanzani INMI Lab Cellular Immunol &
Pharmacol Via Portuense 292 I-00149 Rome Italy;
V gamma 9V delta 2 T-cells; HCV infection; Liver tissue; PhAg;
机译:来自HCV感染患者的肝内Vγ9Vδ2T细胞显示出耗尽的表型,但可以抑制HCV复制
机译:HCV感染的肝细胞通过Umicon表达的上调抑制自噬助焊剂并抑制HCV复制。
机译:预防Vγ9VDelta 2 T细胞活化由Vγ9Vdelta 2 TCR纳米谱(Vol 198,PG 308,2017)
机译:基于表型的具有构象特异性抑制剂的筛选显示P38γ和δ作为肝细胞癌的治疗靶标。
机译:表达Th1表型的Vdelta1 T淋巴细胞是浸入HCV感染者肝脏的主要gammadelta T细胞亚群。
机译:V伽玛9V三角洲2 T细胞无能和互补决定区域3非传染性疟疾发作期间特异性耗竭
机译:Gamma Delta T细胞调节创伤 - 出血后肺部炎症细胞浸润。