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A distinct subset of intestinal dendritic cells responds selectively to oral TLR7/8 stimulation.

Journal article
Authors Ulf Yrlid
Vuk Cerovic
Simon Milling
Christopher D Jenkins
Linda S Klavinskis
G Gordon MacPherson
Published in European journal of immunology
Volume 36
Issue 10
Pages 2639-48
ISSN 0014-2980
Publication year 2006
Published at Institute of Biomedicine, Department of Microbiology and Immunology
Pages 2639-48
Language en
Links dx.doi.org/10.1002/eji.200636426
Keywords Adjuvants, Immunologic, administration & dosage, Administration, Oral, Animals, Chemotaxis, drug effects, immunology, Dendritic Cells, cytology, drug effects, immunology, Enzyme-Linked Immunosorbent Assay, Flow Cytometry, Imidazoles, administration & dosage, Interleukin-12 Subunit p40, secretion, Interleukin-6, secretion, Intestines, cytology, immunology, Liver, cytology, immunology, Lymph, cytology, drug effects, Membrane Glycoproteins, drug effects, immunology, Rats, Reverse Transcriptase Polymerase Chain Reaction, Toll-Like Receptor 7, drug effects, immunology, Toll-Like Receptor 8, drug effects, immunology
Subject categories Microbiology in the medical area

Abstract

The intestinal innate immune system continually interacts with commensal bacteria, thus oral vaccines should induce extra/alternative activation of DC, potentially through TLR. To examine this we collected intestinal lymph DC (iL-DC) under steady-state conditions and after feeding resiquimod (R-848), a synthetic TLR7/8 ligand, which we showed induces complete emptying of gut DC into lymph. iL-DC are heterogeneous with subset-specific functions. In this study we determined the kinetics of iL-DC subset release, activation and cytokine secretion induced by R-848. We show that L-DC comprise three distinct subsets (CD172ahigh, CD172aint and CD172alow) present with similar frequencies in intestinal but not hepatic lymph. No iL-DC express TLR7 mRNA, and only CD172a+ iL-DC express TLR8. However, after oral R-848 administration, output of all three subsets increases dramatically. CD172ahigh DC release precedes that of CD172alow DC, and the increased frequency of CD25high iL-DC is restricted to the two CD172a+ subsets. After feeding R-848 only CD172ahigh iL-DC secrete IL-6 and IL-12p40. However, CD172aint and CD172ahigh DC secrete similar but markedly lower amounts when stimulated in vitro. These results highlight the importance of in vivo approaches to assess adjuvant effects on DC and give novel insights into the subset-specific effects of an oral TLR ligand on intestinal DC.

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