| Literature DB >> 31017652 |
Jingxia Wu1, Sicong Ma1,2, Agnes Hotz-Wagenblatt3, Peter Angel4, Kerstin Mohr1, Tilo Schlimbach1, Michael Schmitt2,5, Guoliang Cui1,6.
Abstract
To maintain immune tolerance, effector T-cell (Teff) responses must be checked by the regulatory T cells (Tregs) in time. It remains incompletely understood how Tregs sense real-time Teff activation. Here, we report that the AP-1 transcription factor JunB, which is induced in Teffs upon T-cell receptor (TCR) activation, is also increased in Tregs by TCR stimuli. Treg-specific deletion of Junb impairs Treg identity, causes uncontrolled inflammatory cytokine production by Teffs and leads to the T-box transcription factor T-bet-dependent spontaneous inflammation. Furthermore, JunB deficiency in Tregs unleashes antitumor Teff responses in a mouse model of melanoma. We conclude that JunB alarms Tregs of the emerging Teff activation and synchronizes immune regulation with the immune reaction in autoimmunity and cancer.Entities:
Keywords: JunB; Tregs; antitumor T cells; autoimmunity; effector T cells
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Year: 2019 PMID: 31017652 DOI: 10.1002/1873-3468.13393
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124