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A population of CD4+ T cells with a naive phenotype stably polarized to the TH1 lineage

Lo, J. W. P.; Vila de Mucha, M.; Roberts, L. B.; Garrido-Mesa, N.; Hertweck, A.; Neves, J. F.; Stolarczyk, E.; Henderson, S.; Jackson, I.; Howard, J. K.; Jenner, R. G.; Lord, G. M.

2020-08-11 immunology
10.1101/2020.07.14.202168 bioRxiv
Show abstract

T-bet is the lineage-specifying transcription factor for CD4+ T helper type 1 (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 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 with naive cell surface markers and that this novel cell population is phenotypically and functionally distinct from conventional naive CD4+ T cells. These cells are also distinct from previously described populations of memory phenotype and stem cell-like T cells. Naive-like T-bet-experienced cells are polarised to the TH1 lineage, predisposed to produce IFN{gamma} upon cell activation, and resist repolarisation to other lineages in vitro and in vivo. These results demonstrate that lineage-specifying factors can function to polarise T cells in the absence of canonical markers of T cell activation and that this has an impact on the subsequent T helper response.

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