The past, present, and future of non-viral CAR T cells

A Moretti, M Ponzo, CA Nicolette… - Frontiers in …, 2022 - frontiersin.org
Adoptive transfer of chimeric antigen receptor (CAR) T lymphocytes is a powerful technology
that has revolutionized the way we conceive immunotherapy. The impressive clinical results …

Comprehensive review of CRISPR-based gene editing: mechanisms, challenges, and applications in cancer therapy

M Chehelgerdi, M Chehelgerdi… - Molecular cancer, 2024 - Springer
The CRISPR system is a revolutionary genome editing tool that has the potential to
revolutionize the field of cancer research and therapy. The ability to precisely target and edit …

High-yield genome engineering in primary cells using a hybrid ssDNA repair template and small-molecule cocktails

BR Shy, VS Vykunta, A Ha, A Talbot, TL Roth… - Nature …, 2023 - nature.com
Enhancing CRISPR-mediated site-specific transgene insertion efficiency by homology-
directed repair (HDR) using high concentrations of double-stranded DNA (dsDNA) with …

Lipid Nanoparticle-Mediated Hit-and-Run Approaches Yield Efficient and Safe In Situ Gene Editing in Human Skin

J Bolsoni, D Liu, F Mohabatpour, R Ebner… - ACS …, 2023 - ACS Publications
Despite exciting advances in gene editing, the efficient delivery of genetic tools to
extrahepatic tissues remains challenging. This holds particularly true for the skin, which …

A highly efficient transgene knock-in technology in clinically relevant cell types

AG Allen, SQ Khan, CM Margulies… - Nature …, 2024 - nature.com
Inefficient knock-in of transgene cargos limits the potential of cell-based medicines. In this
study, we used a CRISPR nuclease that targets a site within an exon of an essential gene …

Homology-independent targeted insertion (HITI) enables guided CAR knock-in and efficient clinical scale CAR-T cell manufacturing

H Balke-Want, V Keerthi, N Gkitsas, AG Mancini… - Molecular Cancer, 2023 - Springer
Abstract Background Chimeric Antigen Receptor (CAR) T cells are now standard of care
(SOC) for some patients with B cell and plasma cell malignancies and could disrupt the …

sustainable clinical development of CAR-T cells–switching from viral transduction towards CRISPR-Cas gene editing

DL Wagner, U Koehl, M Chmielewski… - Frontiers in …, 2022 - frontiersin.org
T cells modified for expression of Chimeric Antigen Receptors (CARs) were the first gene-
modified cell products approved for use in cancer immunotherapy. CAR-T cells engineered …

Combining different CRISPR nucleases for simultaneous knock-in and base editing prevents translocations in multiplex-edited CAR T cells

V Glaser, C Flugel, J Kath, W Du, V Drosdek, C Franke… - Genome Biology, 2023 - Springer
Background Multiple genetic modifications may be required to develop potent off-the-shelf
chimeric antigen receptor (CAR) T cell therapies. Conventional CRISPR-Cas nucleases …

A review on CRISPR/Cas: a versatile tool for cancer screening, diagnosis, and clinic treatment

X Yang, B Zhang - Functional & Integrative Genomics, 2023 - Springer
Cancer is one of the leading causes of death worldwide and it has the trend of increase
incidence. However, in the past decades, as quickly developed new technologies and …

[HTML][HTML] Production and characterization of virus-free, CRISPR-CAR T cells capable of inducing solid tumor regression

KP Mueller, NJ Piscopo, MH Forsberg… - … for immunotherapy of …, 2022 - ncbi.nlm.nih.gov
Background Chimeric antigen receptor (CAR) T cells have demonstrated high clinical
response rates against hematological malignancies (eg, CD19+ cancers) but have shown …