| Literature DB >> 27793593 |
Andrew Jones1, Jessica Bourque1, Lindsey Kuehm1, Adeleye Opejin1, Ryan M Teague1, Cindy Gross1, Daniel Hawiger2.
Abstract
Dendritic cells (DCs) initiate immunity and also antigen-specific tolerance mediated by extrathymic regulatory T (Treg) cells, yet it remains unclear how DCs regulate induction of such tolerance. Here, we report that efficient induction of Treg cells was instructed by BTLA+DEC205+CD8+CD11c+ DCs and the immunomodulatory functions of BTLA. In contrast, T cell activation in steady state by total CD11c+ DCs that include a majority of DCs that do not express BTLA did not induce Treg cells and had no lasting impact on subsequent immune responses. Engagement of HVEM, a receptor of BTLA, promoted Foxp3 expression in T cells through upregulation of CD5. In contrast, T cells activated in the absence of BTLA and HVEM-mediated functions remained CD5lo and therefore failed to resist the inhibition of Foxp3 expression in response to effector cell-differentiating cytokines. Thus, DCs require BTLA and CD5-dependent mechanisms to actively adjust tolerizing T cell responses under steady-state conditions.Entities:
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Year: 2016 PMID: 27793593 PMCID: PMC5112132 DOI: 10.1016/j.immuni.2016.10.008
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745