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@ARTICLE{Poorebrahim:144380,
author = {M. Poorebrahim and S. Sadeghi and E. Fakhr$^*$ and M. F.
Abazari and V. Poortahmasebi and A. Kheirollahi and H.
Askari and A. Rajabzadeh and M. Rastegarpanah and A. Linē
and A. Cid-Arregui$^*$},
title = {{P}roduction of {CAR} {T}-cells by {GMP}-grade lentiviral
vectors: {L}atest advances and future prospects.},
journal = {Critical reviews in clinical laboratory sciences},
volume = {nn},
issn = {1549-781X},
address = {London},
publisher = {Informa Healthcare56466},
reportid = {DKFZ-2019-01833},
pages = {1 - 27},
year = {2019},
abstract = {Chimeric antigen receptor (CAR) T-cells represent a
paradigm shift in cancer immunotherapy and a new milestone
in the history of oncology. In 2017, the Food and Drug
Administration approved two CD19-targeted CAR T-cell
therapies (Kymriah™, Novartis, and Yescarta™, Kite
Pharma/Gilead Sciences) that have remarkable efficacy in
some B-cell malignancies. The CAR approach is currently
being evaluated in multiple pivotal trials designed for the
immunotherapy of hematological malignancies as well as solid
tumors. To generate CAR T-cells ex vivo, lentiviral vectors
(LVs) are particularly appealing due to their ability to
stably integrate relatively large DNA inserts, and to
efficiently transduce both dividing and nondividing cells.
This review discusses the latest advances and challenges in
the design and production of CAR T-cells, and the good
manufacturing practices (GMP)-grade production process of
LVs used as a gene transfer vehicle. New developments in the
application of CAR T-cell therapy are also outlined with
particular emphasis on next-generation allogeneic CAR
T-cells.},
subtyp = {Review Article},
cin = {D015 / D122},
ddc = {570},
cid = {I:(DE-He78)D015-20160331 / I:(DE-He78)D122-20160331},
pnm = {314 - Tumor immunology (POF3-314)},
pid = {G:(DE-HGF)POF3-314},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:31314617},
doi = {10.1080/10408363.2019.1633512},
url = {https://inrepo02.dkfz.de/record/144380},
}