Challenges of CRISPR-Based Gene Editing in Primary T Cells

Adaptive T-cell immunotherapy holds great promise for the successful treatment of leukemia, as well as other types of cancers. More recently, it was also shown to be an effective treatment option for chronic virus infections in immunosuppressed patients. Autologous or allogeneic T cells used for imm...

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Main Authors: Alaleh Rezalotfi, Lea Fritz, Reinhold Förster, Berislav Bošnjak
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/3/1689
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author Alaleh Rezalotfi
Lea Fritz
Reinhold Förster
Berislav Bošnjak
author_facet Alaleh Rezalotfi
Lea Fritz
Reinhold Förster
Berislav Bošnjak
author_sort Alaleh Rezalotfi
collection DOAJ
description Adaptive T-cell immunotherapy holds great promise for the successful treatment of leukemia, as well as other types of cancers. More recently, it was also shown to be an effective treatment option for chronic virus infections in immunosuppressed patients. Autologous or allogeneic T cells used for immunotherapy are usually genetically modified to express novel T-cell or chimeric antigen receptors. The production of such cells was significantly simplified with the CRISPR/Cas system, allowing for the deletion or insertion of novel genes at specific locations within the genome. In this review, we describe recent methodological breakthroughs that were important for the conduction of these genetic modifications, summarize crucial points to be considered when conducting such experiments, and highlight the potential pitfalls of these approaches.
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spelling doaj.art-c78344b7a7f941db8c24699cc35c6e352023-11-23T16:44:54ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-02-01233168910.3390/ijms23031689Challenges of CRISPR-Based Gene Editing in Primary T CellsAlaleh Rezalotfi0Lea Fritz1Reinhold Förster2Berislav Bošnjak3Institute of Immunology, Hannover Medical School, 30625 Hannover, GermanyInstitute of Immunology, Hannover Medical School, 30625 Hannover, GermanyInstitute of Immunology, Hannover Medical School, 30625 Hannover, GermanyInstitute of Immunology, Hannover Medical School, 30625 Hannover, GermanyAdaptive T-cell immunotherapy holds great promise for the successful treatment of leukemia, as well as other types of cancers. More recently, it was also shown to be an effective treatment option for chronic virus infections in immunosuppressed patients. Autologous or allogeneic T cells used for immunotherapy are usually genetically modified to express novel T-cell or chimeric antigen receptors. The production of such cells was significantly simplified with the CRISPR/Cas system, allowing for the deletion or insertion of novel genes at specific locations within the genome. In this review, we describe recent methodological breakthroughs that were important for the conduction of these genetic modifications, summarize crucial points to be considered when conducting such experiments, and highlight the potential pitfalls of these approaches.https://www.mdpi.com/1422-0067/23/3/1689adoptive T-cell therapyCAR T cellsCRISPR/Cas9gene modificationsT cells
spellingShingle Alaleh Rezalotfi
Lea Fritz
Reinhold Förster
Berislav Bošnjak
Challenges of CRISPR-Based Gene Editing in Primary T Cells
International Journal of Molecular Sciences
adoptive T-cell therapy
CAR T cells
CRISPR/Cas9
gene modifications
T cells
title Challenges of CRISPR-Based Gene Editing in Primary T Cells
title_full Challenges of CRISPR-Based Gene Editing in Primary T Cells
title_fullStr Challenges of CRISPR-Based Gene Editing in Primary T Cells
title_full_unstemmed Challenges of CRISPR-Based Gene Editing in Primary T Cells
title_short Challenges of CRISPR-Based Gene Editing in Primary T Cells
title_sort challenges of crispr based gene editing in primary t cells
topic adoptive T-cell therapy
CAR T cells
CRISPR/Cas9
gene modifications
T cells
url https://www.mdpi.com/1422-0067/23/3/1689
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AT leafritz challengesofcrisprbasedgeneeditinginprimarytcells
AT reinholdforster challengesofcrisprbasedgeneeditinginprimarytcells
AT berislavbosnjak challengesofcrisprbasedgeneeditinginprimarytcells