Your browser doesn't support javascript.
loading
A population of naive-like CD4+ T cells stably polarized to the TH 1 lineage.
Lo, Jonathan W; de Mucha, Maria Vila; Henderson, Stephen; Roberts, Luke B; Constable, Laura E; Garrido-Mesa, Natividad; Hertweck, Arnulf; Stolarczyk, Emilie; Houlder, Emma L; Jackson, Ian; MacDonald, Andrew S; Powell, Nick; Neves, Joana F; Howard, Jane K; Jenner, Richard G; Lord, Graham M.
Affiliation
  • Lo JW; School of Immunology and Microbial Sciences, King's College London, London, UK.
  • de Mucha MV; Division of Digestive Diseases, Faculty of Medicine, Imperial College London, London, UK.
  • Henderson S; UCL Cancer Institute and CRUK UCL Centre, University College London (UCL), London, UK.
  • Roberts LB; UCL Cancer Institute and CRUK UCL Centre, University College London (UCL), London, UK.
  • Constable LE; School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Garrido-Mesa N; School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Hertweck A; Division of Digestive Diseases, Faculty of Medicine, Imperial College London, London, UK.
  • Stolarczyk E; School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Houlder EL; School of Life Sciences, Pharmacy and Chemistry, Kingston University, London, UK.
  • Jackson I; UCL Cancer Institute and CRUK UCL Centre, University College London (UCL), London, UK.
  • MacDonald AS; Abcam Plc., Cambridge Biomedical Campus, Cambridge, UK.
  • Powell N; School of Cardiovascular Medicine and Sciences, Guy's Campus, King's College London, London, UK.
  • Neves JF; Lydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
  • Howard JK; School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Jenner RG; Lydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
  • Lord GM; School of Immunology and Microbial Sciences, King's College London, London, UK.
Eur J Immunol ; 52(4): 566-581, 2022 04.
Article in En | MEDLINE | ID: mdl-35092032
ABSTRACT
T-bet is the lineage-specifying transcription factor for CD4+ TH 1 cells. T-bet has also been found in other CD4+ T cell subsets, including TH 17 cells and Treg, where it modulates their functional characteristics. However, we lack information on when and where T-bet is expressed during T cell differentiation and how this impacts T cell differentiation and function. To address this, we traced the ontogeny of T-bet-expressing cells using a fluorescent fate-mapping mouse line. We demonstrate that T-bet is expressed in a subset of CD4+ T cells that have naïve cell surface markers and transcriptional profile and that this novel cell population is phenotypically and functionally distinct from previously described populations of naïve and memory CD4+ T cells. Naïve-like T-bet-experienced cells are polarized to the TH 1 lineage, predisposed to produce IFN-γ upon cell activation, and resist repolarization to other lineages in vitro and in vivo. These results demonstrate that lineage-specifying factors can polarize T cells in the absence of canonical markers of T cell activation and that this has an impact on the subsequent T-helper response.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Th1 Cells / T-Box Domain Proteins Type of study: Prognostic_studies Limits: Animals Language: En Journal: Eur J Immunol Year: 2022 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Th1 Cells / T-Box Domain Proteins Type of study: Prognostic_studies Limits: Animals Language: En Journal: Eur J Immunol Year: 2022 Type: Article Affiliation country: United kingdom