Dataset related to the article "Single- cell profiling defines the prognostic benefit of CD39hi tissue resident memory CD8+ T cells in lumina-like breast cancer"
- 1. Laboratory of Translational Immunology IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan AND Medical Oncology and Hematology Unit; IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan
- 2. Laboratory of Translational Immunology; IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan
- 3. Breast Surgery Unit; IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan
- 4. Department of Pathology; IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan AND Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, 20090 Pieve Emanuele – Milan, Italy
- 5. Humanitas Flow Cytometry Core; IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Mila
- 6. Department of Pathology; IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan
- 7. Genomic Unit, IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan, Italy AND Institute of Genetic and Biomedical Research, UoS Milan, National Research Council, Rozzano, Milan, Italy
- 8. Medical Oncology and Hematology Unit; IRCSS Humanitas Research Hospital, via Manzoni 56, 20089, Rozzano, Milan AND Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, 20090 Pieve Emanuele – Milan, Italy
Description
This record contains data related to the article " Single- cell profiling defines the prognostic benefit of CD39hi tissue resident memory CD8+ T cells in lumina-like breast cancer ".
Luminal-like breast cancer (BC) constitutes the majority of BC subtypes, but, differently from highly aggressive triple negative BC, is poorly infiltrated by the immune system. The quality of the immune infiltrate in luminal-like BCs has been poorly studied, thereby limiting further investigation of immunotherapeutic strategies. By using high-dimensional single-cell technologies, we identify heterogeneous behavior within the tissue-resident memory CD8+ T (Trm) cells infiltrating luminal-like tumors. A subset of CD127- CD39hi Trm cells, preferentially present in the tumor compared to the adjacent normal breast tissue or peripheral blood, retains enhanced degranulation capacity compared to the CD127+ CD39lo Trm counterpart ex vivo, and is specifically associated with positive prognosis. Nevertheless, such prognostic benefit is lost in the presence of highly-suppressive CCR8hi ICOShi IRF4+ effector Tregs. Thus, combinatorial strategies aiming at boosting Trm function and infiltration while relieving from Treg-mediated immunosuppression should be investigated to achieve proper tumor control in luminal-like BCs.
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- Is supplement to
- 10.1038/s42003-021-02595-z (DOI)
- 34552178 (PMID)