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@ARTICLE{Bexte:277341,
author = {T. Bexte and L. M. Reindl and E. Ullrich$^*$},
title = {{N}on-viral technologies can pave the way for {CAR}-{NK}
cell therapy.},
journal = {Journal of leukocyte biology},
volume = {114},
number = {5},
issn = {0741-5400},
address = {Hoboken, NJ},
publisher = {Wiley},
reportid = {DKFZ-2023-01349},
pages = {475-486},
year = {2023},
note = {2023 Oct 26;114(5):475-486},
abstract = {Natural killer (NK) cells are a promising platform for
cancer immunotherapy. NK cells have high intrinsic killing
capability, and the insertion of a chimeric antigen receptor
(CAR) can further enhance their anti-tumor potential. In
first human trials, CAR-NK cells demonstrated strong
clinical activity without therapy-induced side effects. The
applicability of NK cells as an 'off-the-shelf' product
makes them highly attractive for gene-engineered
cell-therapies. Traditionally, viral transduction has been
used for gene-editing; however, the use of viral vectors
remains a safety concern and is associated with high costs
and regulatory requirements. Here, we review the current
landscape of non-viral approaches for CAR-NK cell
generation, which include transfection of vector particles
and electroporation of mRNA and DNA vectors resulting in
transient gene-modification and CAR expression. In addition,
using non-viral transposon technologies, NK cells can be
stably modified ensuring long-lasting CAR expression.
Finally, we discuss CRISPR/Cas9 tools to edit key genes for
NK cell functionality.},
subtyp = {Review Article},
keywords = {CAR (Other) / CRISPR (Other) / electroporation (Other) /
mRNA (Other) / natural killer cell (Other) / non-viral
(Other) / transposon (Other)},
cin = {FM01},
ddc = {570},
cid = {I:(DE-He78)FM01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:37403203},
doi = {10.1093/jleuko/qiad074},
url = {https://inrepo02.dkfz.de/record/277341},
}