达拉图穆马
抗体依赖性细胞介导的细胞毒性
NK-92
多发性骨髓瘤
CD38
白细胞介素21
细胞毒性T细胞
生物
癌症研究
白细胞介素12
脱颗粒
淋巴因子激活杀伤细胞
免疫学
免疫系统
单克隆抗体
抗体
T细胞
细胞生物学
干细胞
川地34
硼替佐米
体外
受体
生物化学
作者
Hyunsoo Cho,Kyung Hwan Kim,Hoyoung Lee,Chang Gon Kim,Haerim Chung,Yoon Seok Choi,Su‐Hyung Park,June‐Won Cheong,Yoo Hong Min,Eui‐Cheol Shin,Jin Seok Kim
标识
DOI:10.1158/1078-0432.ccr-20-3418
摘要
To investigate the different roles of heterogeneous natural killer (NK)-cell subpopulations in multiple myeloma and to identify NK-cell subsets that support the robust anti-myeloma activity of daratumumab via antibody-dependent cellular cytotoxicity (ADCC).We performed single-cell RNA sequencing of NK cells from patients with newly diagnosed multiple myeloma (NDMM) and delineated adaptive NK cells in their bone marrow (BM). We further characterized the distinct immunophenotypic features and functions of adaptive NK cells by multicolor flow cytometry in 157 patients with NDMM.Adaptive NK cells exhibit a significantly lower level of CD38 expression compared with conventional NK cells, suggesting that they may evade daratumumab-induced fratricide. Moreover, adaptive NK cells exert robust daratumumab-mediated effector functions ex vivo, including cytokine production and degranulation, compared with conventional NK cells. The composition of adaptive NK cells in BM determines the daratumumab-mediated ex vivo functional activity of BM NK cells in patients with NDMM. Unlike conventional NK cells, sorted adaptive NK cells from the BM of patients with NDMM exert substantial cytotoxic activity against myeloma cells in the presence of daratumumab.Our findings indicate that adaptive NK cells are an important mediator of ADCC in multiple myeloma and support direct future efforts to better predict and improve the treatment outcome of daratumumab by selectively employing adaptive NK cells.
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