Immunomodulatory role of flagellin in antigen-presenting cells

Toll-like receptors (TLRs) expressed by cells of the immune system play a central role in the generation of immune responses against pathogens. Following TLR ligation, both pro-inflammatory and anti-inflammatory mediators are produced in order to elicit an immune response that controls the microbial...

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Main Author: Vicente-Suarez, Ildefonso
Format: Others
Published: Scholar Commons 2007
Subjects:
DCs
Online Access:http://scholarcommons.usf.edu/etd/2397
http://scholarcommons.usf.edu/cgi/viewcontent.cgi?article=3396&context=etd
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spelling ndltd-USF-oai-scholarcommons.usf.edu-etd-33962015-09-30T04:39:14Z Immunomodulatory role of flagellin in antigen-presenting cells Vicente-Suarez, Ildefonso Toll-like receptors (TLRs) expressed by cells of the immune system play a central role in the generation of immune responses against pathogens. Following TLR ligation, both pro-inflammatory and anti-inflammatory mediators are produced in order to elicit an immune response that controls the microbial infection while limiting tissue damage. Among these mediators, the proinflammatory cytokine IL-12 and the anti-inflammatory cytokine IL-10 are known to play major roles. Here, we show that in vitro or in vivo stimulation with flagellin, the TLR5 ligand, does not result in IL-10 production. Furthermore flagellin inhibits IL-10 production by other specific TLR ligands at the protein and mRNA levels while increasing IL-12p70 production. Several studies have linked the activation of extracellular signal regulated kinases (ERKs) with IL-10 induction by TLRs. Our findings that LPS-induced ERK activation is significantly decreased in flagellin-treated macrophages suggest that this pathway might play a role in the inhibition of IL-10 production by flagellin. Flagellin-mediated IL-10 inhibition was not observed in cells that do not express TLR5 supporting that this effect is TLR5-dependent.Flagellin used as an adjuvant is capable of priming antigen specific T cell responses in an in vivo model of tolerance using high dose peptide. Furthermore, DCs differentiated in tolerogenic conditions (tolerogenic-DCs) express higher levels of TLR5 mRNA than standard BM-DCs and respond more vigorously to flagellin stimulation. Antigen presentation by LPS-matured tolerogenic-DCs results in the differentiation of IL-10 producing T cells with a Tr1-like phenotype. On the contrary, antigen presentation by tolerogenic-DCs that have been stimulated with flagellin results in the differentiation of a typical Th1 responseThis study provides a new insight of the role of flagellin recognition by TLR5 in shaping the immune response elicited by flagellated microorganisms. 2007-06-01T07:00:00Z text application/pdf http://scholarcommons.usf.edu/etd/2397 http://scholarcommons.usf.edu/cgi/viewcontent.cgi?article=3396&context=etd default Graduate Theses and Dissertations Scholar Commons TLR5 Macrophages Toll-like receptors IL-10 DCs American Studies Arts and Humanities
collection NDLTD
format Others
sources NDLTD
topic TLR5
Macrophages
Toll-like receptors
IL-10
DCs
American Studies
Arts and Humanities
spellingShingle TLR5
Macrophages
Toll-like receptors
IL-10
DCs
American Studies
Arts and Humanities
Vicente-Suarez, Ildefonso
Immunomodulatory role of flagellin in antigen-presenting cells
description Toll-like receptors (TLRs) expressed by cells of the immune system play a central role in the generation of immune responses against pathogens. Following TLR ligation, both pro-inflammatory and anti-inflammatory mediators are produced in order to elicit an immune response that controls the microbial infection while limiting tissue damage. Among these mediators, the proinflammatory cytokine IL-12 and the anti-inflammatory cytokine IL-10 are known to play major roles. Here, we show that in vitro or in vivo stimulation with flagellin, the TLR5 ligand, does not result in IL-10 production. Furthermore flagellin inhibits IL-10 production by other specific TLR ligands at the protein and mRNA levels while increasing IL-12p70 production. Several studies have linked the activation of extracellular signal regulated kinases (ERKs) with IL-10 induction by TLRs. Our findings that LPS-induced ERK activation is significantly decreased in flagellin-treated macrophages suggest that this pathway might play a role in the inhibition of IL-10 production by flagellin. Flagellin-mediated IL-10 inhibition was not observed in cells that do not express TLR5 supporting that this effect is TLR5-dependent.Flagellin used as an adjuvant is capable of priming antigen specific T cell responses in an in vivo model of tolerance using high dose peptide. Furthermore, DCs differentiated in tolerogenic conditions (tolerogenic-DCs) express higher levels of TLR5 mRNA than standard BM-DCs and respond more vigorously to flagellin stimulation. Antigen presentation by LPS-matured tolerogenic-DCs results in the differentiation of IL-10 producing T cells with a Tr1-like phenotype. On the contrary, antigen presentation by tolerogenic-DCs that have been stimulated with flagellin results in the differentiation of a typical Th1 responseThis study provides a new insight of the role of flagellin recognition by TLR5 in shaping the immune response elicited by flagellated microorganisms.
author Vicente-Suarez, Ildefonso
author_facet Vicente-Suarez, Ildefonso
author_sort Vicente-Suarez, Ildefonso
title Immunomodulatory role of flagellin in antigen-presenting cells
title_short Immunomodulatory role of flagellin in antigen-presenting cells
title_full Immunomodulatory role of flagellin in antigen-presenting cells
title_fullStr Immunomodulatory role of flagellin in antigen-presenting cells
title_full_unstemmed Immunomodulatory role of flagellin in antigen-presenting cells
title_sort immunomodulatory role of flagellin in antigen-presenting cells
publisher Scholar Commons
publishDate 2007
url http://scholarcommons.usf.edu/etd/2397
http://scholarcommons.usf.edu/cgi/viewcontent.cgi?article=3396&context=etd
work_keys_str_mv AT vicentesuarezildefonso immunomodulatoryroleofflagellininantigenpresentingcells
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