Abstract
T-bet is the lineage-specifying transcription factor for CD4+ TH1 cells. T-bet has also been found in other CD4+ T cell subsets, including TH17 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 TH1 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.
| Original language | English |
|---|---|
| Pages (from-to) | 566-581 |
| Journal | European Journal of Immunology |
| Volume | 52 |
| Issue number | 4 |
| Early online date | 28 Jan 2022 |
| DOIs | |
| Publication status | Published - 30 Apr 2022 |
Keywords
- Immunology
- Immunology and Allergy
- Infection and immunology
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