| Literature DB >> 27346349 |
Junjie Zhang1, Hao Feng2, Jun Zhao1, Emily R Feldman3, Si-Yi Chen1, Weiming Yuan1, Canhua Huang4, Omid Akbari1, Scott A Tibbetts3, Pinghui Feng5.
Abstract
Activation of nuclear factor of activated T cells (NFAT) is crucial for immune responses. IKKε is an IκB kinase (IKK)-related kinase, and the function of IKKε remains obscure in T cells, despite its abundant expression. We report that IKKε inhibits NFAT activation and T cell responses by promoting NFATc1 phosphorylation. During T cell activation, IKKε was transiently activated to phosphorylate NFATc1. Loss of IKKε elevated T cell antitumor and antiviral immunity and, therefore, reduced tumor development and persistent viral infection. IKKε was activated in CD8(+) T cells of mice bearing melanoma or persistently infected with a model herpesvirus. These results collectively show that IKKε promotes NFATc1 phosphorylation and inhibits T cell responses, identifying IKKε as a crucial negative regulator of T cell activation and a potential target for immunotherapy.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27346349 PMCID: PMC5293007 DOI: 10.1016/j.celrep.2016.05.083
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423