Generation and validation of CRISPR-engineered human natural killer cell lines for research and therapeutic applications
Cytotoxic natural killer cells kill tumors and infected cells. We carried out CRISPR-based gene editing and transcriptional regulation in hard-to-manipulate NK-92 cells. NK-92-based therapies were found to be safe and efficacious in preclinical studies of cancers. Here, we have pioneered the generat...
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Veröffentlicht in: | STAR protocols 2021-12, Vol.2 (4), p.100874-100874, Article 100874 |
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Sprache: | eng |
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Zusammenfassung: | Cytotoxic natural killer cells kill tumors and infected cells. We carried out CRISPR-based gene editing and transcriptional regulation in hard-to-manipulate NK-92 cells. NK-92-based therapies were found to be safe and efficacious in preclinical studies of cancers. Here, we have pioneered the generation and validation of NK-92 cells constitutively expressing Cas9 or dCas9 for knockout (CRISPRko), transcriptional activation (CRISPRa), or transcriptional repression (CRISPRi) of genes. Our CRISPR-engineered NK-92 cell platforms can be modified for research and off-the-shelf therapeutic applications.
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•Constitutively repressing or activating genes in human NK cells is difficult•CRISPR-engineered natural killer cells are attractive for therapeutic applications•Our approach generates stable CRISPRko, CRISPRi, and CRISPRa human NK cell lines
Cytotoxic natural killer cells kill tumors and infected cells. We carried out CRISPR-based gene editing and transcriptional regulation in hard-to-manipulate NK-92 cells. NK-92-based therapies were found to be safe and efficacious in preclinical studies of cancers. Here, we have pioneered the generation and validation of NK-92 cells constitutively expressing Cas9 or dCas9 for knockout (CRISPRko), transcriptional activation (CRISPRa), or transcriptional repression (CRISPRi) of genes. Our CRISPR-engineered NK-92 cell platforms can be modified for research and off-the-shelf therapeutic applications. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2021.100874 |