医学
免疫疗法
多发性骨髓瘤
细胞疗法
颗粒酶B
颗粒酶
归巢(生物学)
移植
离体
免疫学
癌症研究
自体干细胞移植
干细胞
骨髓
白细胞介素21
穿孔素
体内
免疫系统
T细胞
内科学
生物
CD8型
细胞生物学
生物技术
生态学
作者
Hareth Nahi,Michael Chrobok,Stephan Meinke,Charlotte Gran,Nicole Marquardt,Gabriel Afram,Tolga Sütlü,Mari Gilljam,Birgitta Stellan,Arnika Kathleen Wagner,Pontus Blomberg,Per-Henrik Holmqvist,Lilian Walther–Jallow,Karin Mellström,Johan Liwing,Charlotte Gustafsson,Robert Månsson,Monika Klimkowska,Gösta Gahrton,Johan Lund
标识
DOI:10.1016/j.xcrm.2022.100508
摘要
Few approaches have been made toward exploring autologous NK cells in settings of cancer immunotherapy. Here, we demonstrate the feasibility of infusing multiple doses of ex vivo activated and expanded autologous NK cells in patients with multiple myeloma (MM) post-autologous stem cell transplantation. Infused NK cells were detected in circulation up to 4 weeks after the last infusion. Elevations in plasma granzyme B levels were observed following each consecutive NK cell infusion. Moreover, increased granzyme B levels were detected in bone marrow 4 weeks after the last infusion. All measurable patients had objective, detectable responses after NK cell infusions in terms of reduction in M-component and/or minimal residual disease. The present study demonstrates that autologous NK cell-based immunotherapy is feasible in a setting of MM consolidation therapy. It opens up the possibility for usage of autologous NK cells in clinical settings where patients are not readily eligible for allogeneic NK cell-based immunotherapies.
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