First Trial of CRISPR-Edited T cells in Lung Cancer

The clinical application of CRISPR-Cas9 gene editing has been eagerly awaited since the first description of the technique in 2013. Lu and colleagues now describe the treatment of 12 patients with nonsmall-cell lung cancer (NSCLC) with PD-1 gene-edited bulk autologous T cells, with results supportin...

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Veröffentlicht in:Trends in molecular medicine 2020-08, Vol.26 (8), p.713-715
Hauptverfasser: Lacey, Simon F., Fraietta, Joseph A.
Format: Artikel
Sprache:eng
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Zusammenfassung:The clinical application of CRISPR-Cas9 gene editing has been eagerly awaited since the first description of the technique in 2013. Lu and colleagues now describe the treatment of 12 patients with nonsmall-cell lung cancer (NSCLC) with PD-1 gene-edited bulk autologous T cells, with results supporting both the feasibility and safety of gene editing in cell therapy.
ISSN:1471-4914
1471-499X
DOI:10.1016/j.molmed.2020.06.001