| Literature DB >> 32536469 |
Simon F Lacey1, Joseph A Fraietta2.
Abstract
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.Entities:
Mesh:
Year: 2020 PMID: 32536469 DOI: 10.1016/j.molmed.2020.06.001
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951