关键词: CD48 Contact stability NK-cell therapy NSCLC Susceptibility

Mesh : Blotting, Western CD48 Antigen / immunology metabolism Carcinoma, Non-Small-Cell Lung / immunology metabolism Cell Line, Tumor Flow Cytometry Humans Killer Cells, Natural / immunology physiology Lung Neoplasms / immunology metabolism Polymerase Chain Reaction

来  源:   DOI:10.1007/s12272-021-01365-z

Abstract:
The susceptibility of cancer cells to natural killer (NK) cell-mediated cytotoxicity depends on the balance of activating and inhibitory ligands expressed on their surface. Although many types of cancer cells are killed by NK cells, non-small-cell lung cancer (NSCLC) cells are relatively resistant to NK cell-mediated cytotoxicity. In this study, we showed that several NSCLC cell lines have differential sensitivity to NK cell-mediated cytotoxicity: NCI-H522 cells were highly sensitive, but A549, NCI-H23, NCI-H1915, and NCI-H1299 were resistant. Among activating ligands such as CD48, HLA-A/B/G, ICAM-1, MICA/B, and ULBPs, only CD48 rendered NCI-H522 cells susceptible to NK cell-mediated cytotoxicity, which was proved by using CD48 siRNA and neutralizing antibody. CD48-positive NCI-H522 cells established a more stable contact with NK cells than did CD48-negative A549 and CD48 siRNA cell-transfected NCI-H522 cells. Taken together, these data demonstrate that CD48-positive NSCLC cells might be susceptible to NK cell-mediated cytotoxicity, which provide information on how to stratify NSCLC patients potentially responsive to NK-cell therapy.
摘要:
暂无翻译
公众号