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Genre/Form: | Thèses et écrits académiques |
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Material Type: | Document, Thesis/dissertation |
Document Type: | Computer File |
All Authors / Contributors: |
Adeline Crinier; Éric Vivier, biologiste).; Émilie Narni-Mancinelli; Franck Galland; Anne Caignard; Nadine Cerf-Bensussan; Aix-Marseille Université.; Ecole Doctorale Sciences de la Vie et de la Santé (Marseille).; Centre d'Immunologie Marseille-Luminy (CIML). |
OCLC Number: | 1229950516 |
Notes: | Titre provenant de l'écran-titre. |
Description: | 1 online resource |
Responsibility: | Adeline Crinier ; sous la direction de Éric Vivier et de Émilie Narni-Mancinelli. |
Abstract:
NK cells and helper-like ILCs (ILC1, ILC2, ILC3) are part of the family of innate lymphoid cells (ILC). Single-cell RNAseq (scRNAseq) is emerging as a powerful tool whose applications will have meaningful implications for both basic and clinical research.Through the use of scRNAseq, we identified the existence of several subpopulations of splenic NK cells, 4 in human, 3 in the mouse and 2 subsets in the blood of both human and mouse blood. The transcriptomic profiles of the two major subsets, NK1 (resembling CD56dim NK cells in human and CD27-CD11b+ NK cells in mouse) and NK2 (resembling CD56bright NK cells human and CD27-CD11b+ NK cells in mouse), were similar across organs and species.In human bone marrow, our second study confirmed the presence of NK1 and NK2 and characterized a second subset of CD56bright NK cells subset (NK0) as the precursor of both circulating CD56bright NK2-like and CD56dim NK1-like NK cells. In patients with acute myeloid leukemia (AML), transcriptomic profiles of NK cells are altered, with a stress-induced repression of NK cell effector functions relative to healthy NK cells. In tumors of patients suffering from colorectal cancer (CRC), we identified an additional ILC1-like subsets and infiltrating ILC2, both absent from healthy tissue. Moreover, we found that tumor-infiltrating and blood ILC from CRC patients exhibited higher levels of SLAMF1 on. Lastly, SLAMF1-high group of rectal cancer patients has a significantly higher survival rate than the SLAMF1-low patients. SLAMF1 is therefore a biomarker of CRC.
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