Abstract

Elevated levels of systemic IL-10 have been associated with several chronic viral infections, including HCV, EBV, HCMV and LCMV. In the chronic LCMV infection model, both elevated IL-10 and enhanced infection of dendritic cells (DCs) are important for viral persistence. This report highlights the relationship between enhanced viral tropism for DCs and the induction of IL-10 in CD4 T cells, which we identify as the most frequent IL-10-expressing cell type in chronic LCMV infection. Here we report that infected CD8αneg DCs express elevated IL-10, induce IL-10 expression in LCMV specific CD4 T cells, and suppress LCMV-specific T cell proliferation. DCs exposed in vivo to persistent LCMV retain the capacity to stimulate CD4 T cell proliferation but induce IL-10 production by both polyclonal and LCMV-specific CD4 T cells. Our study delineates the unique effects of direct infection versus viral exposure on DCs. Collectively these data point to enhanced infection of DCs as a key trigger of the IL-10 induction cascade resulting in maintenance of elevated IL-10 expression in CD4 T cells and inhibition of LCMV-specific CD4 and CD8 T cell proliferation.

Highlights

  • The host-pathogen relationship in chronic viral infections requires the establishment of equilibrium between the host immune response and viral replication

  • In this study we set out to determine which cell types would produce IL-10 in response to Clone 13 (Cl13) infection in vivo, and what role enhanced viral tropism for dendritic cells (DCs) may play in the induction and maintenance of elevated IL-10 levels during Cl13 infection

  • We report that directly infected, in contrast to virally exposed, CD8aneg DCs from Cl13-infected mice express elevated IL-10 and suppress CD4 and CD8 T cell proliferation in vitro

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Summary

Introduction

The host-pathogen relationship in chronic viral infections requires the establishment of equilibrium between the host immune response and viral replication. While this balance of competing interests aids in protecting the host from the immunopathologic consequences of continuous inflammation, such a truce can result in the prolonged persistence of the virus within its host. Enhanced dendritic cell (DC) infection, elevated IL-10 expression and rapid T cell exhaustion (a state of diminished effector function, increased inhibitory receptor expression and altered transcriptional profiles), are hallmarks of chronic, but not acute, lymphocytic choriomeningitis (LCMV) infection [3,5,10,11,12,13,14,15,16]

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