Journal
CELL
Volume 175, Issue 7, Pages 1958-+Publisher
CELL PRESS
DOI: 10.1016/j.cell.2018.10.024
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Funding
- Parker Institute for Cancer Immunotherapy (PICI)
- Career Award for Medical Scientists from the Burroughs Wellcome Fund
- Innovative Genomics Institute (IGI)
- Damon Runyon Physician-Scientist Training Award [PST-08-16]
- Diabetes Research Center [NIH P30 DK063720]
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Human T cells are central effectors of immunity and cancer immunotherapy. CRISPR-based functional studies in T cells could prioritize novel targets for drug development and improve the design of genetically reprogrammed cell-based therapies. However, large-scale CRISPR screens have been challenging in primary human cells. We developed a new method, single guide RNA (sgRNA) lentiviral infection with Cas9 protein electroporation (SLICE), to identify regulators of stimulation responses in primary human T cells. Genome-wide loss-of-function screens identified essential T cell receptor signaling components and genes that negatively tune proliferation following stimulation. Targeted ablation of individual candidate genes characterized hits and identified perturbations that enhanced cancer cell killing. SLICE coupled with single-cell RNA sequencing (RNA-seq) revealed signature stimulation-response gene programs altered by key genetic perturbations. SLICE genome-wide screening was also adaptable to identify mediators of immunosuppression, revealing genes controlling responses to adenosine signaling. The SLICE platform enables unbiased discovery and characterization of functional gene targets in primary cells.
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