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Early T-bet promotes LFA1 upregulation required for CD8(+) effector and memory T cell development
The T-box transcription factor T-bet is regarded as a “master regulator” of CD4(+) Th1 differentiation and IFN-γ production. However, in multiple models of infection, T-bet appears less critical for CD8(+) T cell expansion and effector function. Here, we show that following vaccination with a replic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712775/ https://www.ncbi.nlm.nih.gov/pubmed/36445307 http://dx.doi.org/10.1084/jem.20191287 |
Sumario: | The T-box transcription factor T-bet is regarded as a “master regulator” of CD4(+) Th1 differentiation and IFN-γ production. However, in multiple models of infection, T-bet appears less critical for CD8(+) T cell expansion and effector function. Here, we show that following vaccination with a replication-deficient strain of Toxoplasma gondii, CD8(+) T cell expression of T-bet is required for optimal expansion of parasite-specific effector CD8(+) T cells. Analysis of the early events associated with T cell activation reveals that the α chain of LFA1, CD11a, is a target of T-bet, and T-bet is necessary for CD8(+) T cell upregulation of this integrin, which influences the initial priming of CD8(+) effector T cells. We propose that the early expression of T-bet represents a T cell–intrinsic factor that optimizes T–DC interactions necessary to generate effector responses. |
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