The NK-92 cell line-30 years later: its impact on natural killer cell research and treatment of cancer

被引:72
作者
Klingemann, Hans [1 ,2 ]
机构
[1] ImmunityBio Inc, Culver City, CA USA
[2] ImmunityBio Inc, 9920 Jefferson Blvd, Culver City, CA 90232 USA
关键词
ADCC; CAR; Cytotoxicity; NK-92; NK cell lines; NK cells; IMMUNOTHERAPY; TRIAL; MELANOMA;
D O I
10.1016/j.jcyt.2022.12.003
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The NK-92 cell line, established in 1992, mirrors all the characteristics of highly active blood natural killer (NK) cells but with much broader and greater cytotoxicity. The cell line was established from the blood cells of a patient with lymphoma and has been made widely available for research since it was deposited into the American Type Culture Collection in 1998. The worldwide distribution of NK-92 cells has led to a plethora of scientific discoveries that have greatly increased the understanding of NK-cell biology. NK-92 cells also have been developed for clinical use, overcoming the challenges of obtaining and expanding NK cells from donor or patient blood. More than 100 patients with cancer have now been treated all over the world with unmodified or genetically engineered NK-92 cells. Modified cells include high-affinity Fc-receptor expressing NK-92 cells (haNKR) and various chimeric antigen receptor targeted haNK cells (t-haNKTM). Infusions of either unmodified or modified NK-92 cells have been reported to be safe and efficacious, leading in some cases to disease remission even in patients who had failed multiple previous lines of therapy. It is the purpose of this review to distill the plethora of scientific data on NK-92 cells and its genetic variants, highlighting relevant experimental findings that have contributed to a better understanding of NK cell biology and summarize the therapeutic potential of these cells for treatment of cancer and infections. (c) 2022 International Society for Cell & Gene Therapy. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:451 / 457
页数:7
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