CD33
髓系白血病
细胞因子释放综合征
医学
耐火材料(行星科学)
急性白血病
不利影响
白血病
癌症研究
临床试验
白细胞介素12
免疫学
癌症
内科学
肿瘤科
嵌合抗原受体
免疫疗法
干细胞
细胞毒性T细胞
体外
川地34
生物
天体生物学
生物化学
遗传学
作者
Xiaowen Tang,Lin Yang,Zheng Li,Ansel P. Nalin,Haiping Dai,Tao Xu,Jia Yin,Fengming You,Mingqing Zhu,Weihua Shen,Guanghua Chen,Xiaofan Zhu,Depei Wu,Jianhua Yu
出处
期刊:PubMed
日期:2018-01-01
卷期号:8 (6): 1083-1089
被引量:177
摘要
CAR T cells have shown clinical efficacy for acute lymphoblastic leukemia, but this therapy has not been effective for acute myeloid leukemia (AML), and other treatment options are needed. Theoretically, CAR-NK cells have a more favorable toxicity profile compared to CAR T cells, especially in avoiding adverse effects such as cytokine release syndrome. However, the clinical evidence for this has not yet been reported. In the current study, we tested the safety of CD33-CAR NK cells in patients with relapsed and refractory AML. At doses up to 5 × 109 (5 billion) cells per patient, no significant adverse effects were observed. CAR NK-92 cells can be produced at much lower cost compared to CAR T cells, and we believe after being optimized, they will be widely accessible for the treatment of cancer.
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