Dataset related to article "Two subsets of stem-like CD8+ memory T cell progenitors with distinct fate commitments in humans".
Authors/Creators
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Galletti, Giovanni1
- De Simone, Gabriele1
- Mazza, Emilia1
- Puccio, Simone1
- Mezzanotte, Claudia2
- Bi, Timothy3
- Davydov, Alexey4
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Metsger, Maria4
- Scamardella, Eloise1
- Alvisi, Giorgia1
- De Paoli, Federica1
- Zanon, Veronica1
- Scarpa, Alice1
- Camisa, Barbara2
- Colombo, Federico5
- Anselmo, Achille5
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Peano, Clelia6
- Polletti, Sara7
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Mavilio, Domenico8
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Gattinoni, Luca9
- Boi, Shannon10
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Youngblood, Benjamin10
- Jones, Rhiannon11
- Baird, Duncan11
- Gostick, Emma12
- Llewellyn-Lacey, Sian12
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Ladell, Kristin12
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Price, David13
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Chudakov, Dmitriy14
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Newell, Evan3
- Casucci, Monica2
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Lugli, Enrico15
- 1. Laboratory of Translational Immunology, Humanitas Clinical and Research Center – IRCCS, Rozzano, Milan, Italy
- 2. Innovative Immunotherapies Unit, Division of Immunology, Transplantation, and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy
- 3. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
- 4. Central European Institute of Technology, Brno, Czech Republic
- 5. Humanitas Flow Cytometry Core, Humanitas Clinical and Research Center – IRCCS, Rozzano, Milan, Italy
- 6. Institute of Genetic and Biomedical Research, UoS Milan, National Research Council, Rozzano, Milan, Italy AND Genomic Unit, Humanitas Clinical and Research Center – IRCCS, Rozzano, Milan, Italy
- 7. Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy
- 8. Unit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center – IRCCS, Rozzano, Milan, Italy AND Department of Medical Biotechnologies and Translational Medicine, University of Milan, Milan, Italy
- 9. Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA AND Regensburg Center for Interventional Immunology, Regensburg, Germany AND University of Regensburg, Regensburg, Germany
- 10. St. Jude Children's Research Hospital, Memphis, TN, USA
- 11. Division of Cancer and Genetics, Cardiff University School of Medicine, Cardiff, UK
- 12. Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK
- 13. Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK AND Systems Immunity Research Institute, Cardiff University School of Medicine, Cardiff, UK
- 14. Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Moscow, Russia AND Pirogov Russian National Research Medical University, Moscow, Russia AND Center of Life Sciences, Skolkovo Institute of Science and Technology, Moscow, Russia
- 15. Laboratory of Translational Immunology, Humanitas Clinical and Research Center – IRCCS, Rozzano, Milan, Italy AND Humanitas Flow Cytometry Core, Humanitas Clinical and Research Center – IRCCS, Rozzano, Milan, Italy
Description
This record contains data related to article “Two subsets of stem-like CD8+ memory T cell progenitors with distinct fate commitments in humans”.
ABSTRACT
T cell memory relies on the generation of antigen-specific progenitors with stem-like properties. However, the identity of these progenitors has remained unclear, precluding a full understanding of the differentiation trajectories that underpin the hetero- geneity of antigen-experienced T cells. We used a systematic approach guided by single-cell RNA-sequencing data to map the organizational structure of the human CD8+ memory T cell pool under physiological conditions. We identified two previously unrecognized subsets of clonally, epigenetically, functionally, phenotypically and transcriptionally distinct stem-like CD8+ memory T cells. Progenitors lacking the inhibitory receptors programmed death-1 (PD-1) and T cell immunoreceptor with Ig and ITIM domains (TIGIT) were committed to a functional lineage, whereas progenitors expressing PD-1 and TIGIT were committed to a dysfunctional, exhausted-like lineage. Collectively, these data reveal the existence of parallel differentiation programs in the human CD8+ memory Tcell pool, with potentially broad implications for the development of immunotherapies and vaccines.
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- Is supplement to
- 10.1038/s41590-020-0791-5 (DOI)
- 33046887 (PMID)