| Literature DB >> 29885993 |
Alexander Nelson1, Christina Cunha2, Michael I Nishimura3, Makio Iwashima4.
Abstract
TNF is a multifunctional cytokine that is critical to host defense against pathogens but can also drive the pathophysiology of inflammatory diseases. Inhibition of TNF occasionally causes exacerbation of some autoimmune diseases, suggesting a role for TNF in the regulation of immune homeostasis. Here, we demonstrate that human peripheral blood CD4+CD25+Foxp3+ regulatory T cells (Tregs) express membrane-bound TNF, a potent activator of the type 2 TNF receptor. While the type 1 TNF receptor can cause cell death and is expressed ubiquitously, the type 2 receptor promotes cell growth and its expression is limited mainly to immune and endothelial cells. When autocrine TNF is blocked in an in vitro culture without IL-2, activated Tregs stop proliferating. These data indicate a novel role for TNF as a Treg-derived autocrine growth factor.Entities:
Keywords: Foxp3; IL-2; TNF; Treg
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Year: 2018 PMID: 29885993 PMCID: PMC6281785 DOI: 10.1016/j.cyto.2018.05.036
Source DB: PubMed Journal: Cytokine ISSN: 1043-4666 Impact factor: 3.861