| Literature DB >> 11970964 |
Ryan A Wilcox1, Andrei I Chapoval, Kevin S Gorski, Mizuto Otsuji, Tahiro Shin, Dallas B Flies, Koji Tamada, Robert S Mittler, Haruo Tsuchiya, Drew M Pardoll, Lieping Chen.
Abstract
Interaction between dendritic cells (DCs) and T cells is a prerequisite for the initiation of a T cell response. The molecular nature of this interaction remains to be fully characterized. We report in this work that freshly isolated mouse splenic DCs and bone marrow-derived DCs express CD137 on the cell surface and in soluble form. Triggering CD137 increased the secretion of IL-6 and IL-12 from DCs. More importantly, infusion of an agonistic mAb to CD137 into naive mice enhanced the ability of DCs to stimulate T cell proliferation in response to both alloantigens and a nominal Ag in vitro. This enhancement of DC function is not mediated through activation of T cells, because the effect was also observed in RAG-1 knockout mice that lack T cells. Our findings implicate CD137 as an important receptor involved in the modulation of DC function.Entities:
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Year: 2002 PMID: 11970964 DOI: 10.4049/jimmunol.168.9.4262
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422