Cutting Edge: Expression of Functional CD137 Receptor by Dendritic Cells

Ryan A. Wilcox(Mayo Clinic), Andrei I. Chapoval(Mayo Clinic), Kevin Gorski(Johns Hopkins University), Mizuto Otsuji(Johns Hopkins University), Tahiro Shin(Johns Hopkins University), Dallas B. Flies(Mayo Clinic), Koji Tamada(Mayo Clinic), Robert S. Mittler(Emory University), Haruo Tsuchiya(Johns Hopkins University), Drew M. Pardoll(Johns Hopkins University), Lieping Chen(Mayo Clinic)
The Journal of Immunology
May 1, 2002
Cited by 228Open Access
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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.


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