Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/214354
Title: Lineage origin and transcriptional control of autoantigen-specific T-regulatory type 1 cells
Author: Angelats Canals, Edgar
Santamaria Vilanova, Pere
Keywords: Cèl·lules T
Nanomedicina
T cells
Nanomedicine
Issue Date: 25-Sep-2023
Publisher: Frontiers
Abstract: T Regulatory type-1 (TR1) cells represent an immunosuppressive T cell subset, discovered over 25 years ago, that produces high levels of interleukin-10 (IL-10) but, unlike its FoxP3+ T regulatory (Treg) cell counterpart, does not express FoxP3 or CD25. Experimental evidence generated over the last few years has exposed a promising role for TR1 cells as targets of therapeutic intervention in immune-mediated diseases. The discovery of cell surface markers capable of distinguishing these cells from related T cell types and the application of next generation sequencing techniques to defining their transcriptional make-up have enabled a more accurate description of this T cell population. However, the developmental biology of TR1 cells has long remained elusive, in particular the identity of the cell type(s) giving rise to bona fide TR1 cells in vivo. Here, we review the fundamental phenotypic, transcriptional and functional properties of this T cell subset, and summarize recent lines of evidence shedding light into its ontogeny.
Note: Reproducció del document publicat a: https://doi.org/10.3389/fimmu.2023.1267697
It is part of: Frontiers In Immunology, 2023, vol. 14
URI: https://hdl.handle.net/2445/214354
Related resource: https://doi.org/10.3389/fimmu.2023.1267697
ISSN: 1664-3224
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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