Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Pritchard, Gretchen Harms, Phan, Anthony T., Christian, David A., Blain, Trevor J., Fang, Qun, Johnson, John, Roy, Nathan H., Shallberg, Lindsey, Kedl, Ross M., Hunter, Christopher A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
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
Descripción
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.