Next generation natural killer cells for cancer immunotherapy: the promise of genetic engineering

被引:166
作者
Daher, May [1 ]
Rezvani, Katayoun [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
关键词
CHIMERIC ANTIGEN RECEPTOR; BETA SIGNALING PATHWAY; OFF-THE-SHELF; TUMOR-CELLS; NK CELLS; T-CELL; IMMUNE EVASION; STEM-CELLS; LINE NK-92; IN-VITRO;
D O I
10.1016/j.coi.2018.03.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent advances in the field of cellular therapy have focused on autologous T cells engineered to express a chimeric antigen receptor (CAR) against tumor antigens. Remarkable responses have been observed in patients receiving autologous CD19-redirected T cells for the treatment of B-lymphoid malignancies. However, the generation of autologous products for each patient is logistically challenging and expensive. Extensive research efforts are ongoing to generate an off-theshelf cellular product for the treatment of cancer patients. Natural killer (NK) cells are attractive contenders since they have potent anti-tumor activity, and their safety in the allogeneic setting expands the cell sources for NK cell therapy beyond an autologous one. In this review, we discuss advantages and limitations of NK cellular therapy, and novel genetic engineering strategies that may be applied to overcome some of the limitations. Next-generation engineered NK cells are showing great promise in the preclinical setting and it is likely that in the next few years CAR-engineered NK cells will be incorporated into the current armamentarium of cell-based cancer therapeutics.
引用
收藏
页码:146 / 153
页数:8
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