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Opposing Development of Cytotoxic and Follicular Helper CD4 T Cells Controlled by the TCF-1-Bcl6 Nexus.


ABSTRACT: CD4+ T cells develop distinct and often contrasting helper, regulatory, or cytotoxic activities. Typically a property of CD8+ T cells, granzyme-mediated cytotoxic T cell (CTL) potential is also exerted by CD4+ T cells. However, the conditions that induce CD4+ CTLs are not entirely understood. Using single-cell transcriptional profiling, we uncover a unique signature of Granzyme B (GzmB)+ CD4+ CTLs, which distinguishes them from other CD4+ T helper (Th) cells, including Th1 cells, and strongly contrasts with the follicular helper T (Tfh) cell signature. The balance between CD4+ CTL and Tfh differentiation heavily depends on the class of infecting virus and is jointly regulated by the Tfh-related transcription factors Bcl6 and Tcf7 (encoding TCF-1) and by the expression of the inhibitory receptors PD-1 and LAG3. This unique profile of CD4+ CTLs offers targets for their study, and its antagonism by the Tfh program separates CD4+ T cells with either helper or killer functions.

SUBMITTER: Donnarumma T 

PROVIDER: S-EPMC5149578 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature

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CD4<sup>+</sup> T cells develop distinct and often contrasting helper, regulatory, or cytotoxic activities. Typically a property of CD8<sup>+</sup> T cells, granzyme-mediated cytotoxic T cell (CTL) potential is also exerted by CD4<sup>+</sup> T cells. However, the conditions that induce CD4<sup>+</sup> CTLs are not entirely understood. Using single-cell transcriptional profiling, we uncover a unique signature of Granzyme B (GzmB)<sup>+</sup> CD4<sup>+</sup> CTLs, which distinguishes them from ot  ...[more]

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