期刊
NATURE BIOTECHNOLOGY
卷 40, 期 12, 页码 -出版社
NATURE PORTFOLIO
DOI: 10.1038/s41587-022-01377-0
关键词
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资金
- H2020 European Research Council [759296 570]
- Israel Science Foundation [1632/16, 2157/16, 2876/21]
- Israeli Health Ministry [0604216191]
- National Institutes of Health [R01 AI167003-01]
- European Research Council [759296, 945674]
- Gertner Institute Scholarship
- Yoran Institute Scholarship
- SAIA Foundation
- SCGC Tel Aviv University
- Israel Cancer Research Foundation Development Award
- Israel Cancer Research Foundation Gesher Award
- Azrieli Faculty Fellowship
- Alon Fellowship for Outstanding Young Scientists
- Israel Council for Higher Education
- Edmond J. Safra Center Fellowship for Bioinformatics at Tel Aviv University
- European Research Council (ERC) [945674, 759296] Funding Source: European Research Council (ERC)
In this study, the outcomes of genome editing in CRISPR-Cas9 transfected primary human T cells were investigated using single-cell RNA sequencing. The study revealed that chromosomal abnormalities and truncations are common outcomes of CRISPR-Cas9 cleavage, and are associated with reduced cell proliferation and cell death.
Multiple clinical trials of allogeneic T cell therapy use site-specific nucleases to disrupt T cell receptor (TCR) and other genes(1-6). In this study, using single-cell RNA sequencing, we investigated genome editing outcomes in primary human T cells transfected with CRISPR-Cas9 and guide RNAs targeting genes for TCR chains and programmed cell death protein 1. Four days after transfection, we found a loss of chromosome 14, harboring the TCR alpha locus, in up to 9% of the cells and a chromosome 14 gain in up to 1.4% of the cells. Chromosome 7, harboring the TCR beta locus, was truncated in 9.9% of the cells. Aberrations were validated using fluorescence in situ hybridization and digital droplet PCR. Aneuploidy was associated with reduced proliferation, induced p53 activation and cell death. However, at 11 days after transfection, 0.9% of T cells still had a chromosome 14 loss. Aneuploidy and chromosomal truncations are, thus, frequent outcomes of CRISPR-Cas9 cleavage that should be monitored and minimized in clinical protocols.
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