Differentiation of natural killer cells from induced pluripotent stem cells under defined, serum- and feeder-free conditions-Reference-Cited by-同舟云学术

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Differentiation of natural killer cells from induced pluripotent stem cells under defined, serum- and feeder-free conditions

Published:2021-10 Issue:10 Volume:23 Page:939-952
ISSN:1465-3249
Container-title:Cytotherapy
language:en
Short-container-title:Cytotherapy

Author:

Lupo Kyle B.,Moon Jung-Il,Chambers Andrea M.,Matosevic Sandro

Publisher

Elsevier BV

Subject

Cancer Research,Transplantation,Cell Biology,Genetics (clinical),Oncology,Immunology,Immunology and Allergy

Reference48 articles.

1. Natural Killer Cells in Cancer Immunotherapy;Miller;Annu Rev Cancer Biol,2019

2. Challenges of NK cell-based immunotherapy in the new era;Fang;Front Med,2018

3. Role of Natural Killer Cell Alloreactivity in HLA-Mismatched Hematopoietic Stem Cell Transplantation;Ruggeri;Blood,1999

4. Effectiveness of donor natural killer cell alloreactivity in mismatched hematopoietic transplants;Ruggeri;Science,2002

5. NK Cells Mediate a Crucial Graft-versus-Leukemia Effect in Haploidentical-HSCT to Cure High-Risk Acute Leukemia;Locatelli;Trends Immunol,2018

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A scalable, spin‐free approach to generate enhanced induced pluripotent stem cell–derived natural killer cells for cancer immunotherapy;Immunology & Cell Biology;2024-09-13

2. Antitumor effects of natural killer cells derived from gene-engineered human induced pluripotent stem cells on hepatocellular carcinoma;2024-08-13

3. Emerging roles of CAR-NK cell therapies in tumor immunotherapy: current status and future directions;Cell Death Discovery;2024-07-10

4. Feeder-free differentiation of human iPSCs into natural killer cells with cytotoxic potential against malignant brain rhabdoid tumor cells;Bioactive Materials;2024-06

5. synNotch-programmed iPSC-derived NK cells usurp TIGIT and CD73 activities for glioblastoma therapy;Nature Communications;2024-03-01

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