A unique dermal dendritic cell subset that skews the immune response toward Th2.

Dendritic cell (DC) subsets in the skin and draining lymph nodes (LNs) are likely to elicit distinct immune response types. In skin and skin-draining LNs, a dermal DC subset expressing macrophage galactose-type C-type lectin 2 (MGL2/CD301b) was found distinct from migratory Langerhans cells (LCs) or...

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Main Authors: Ryuichi Murakami, Kaori Denda-Nagai, Shin-ichi Hashimoto, Shigenori Nagai, Masahira Hattori, Tatsuro Irimura
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3767795?pdf=render
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spelling doaj-03619517c0ee4c6cb48ebe089e50e80f2020-11-24T21:54:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7327010.1371/journal.pone.0073270A unique dermal dendritic cell subset that skews the immune response toward Th2.Ryuichi MurakamiKaori Denda-NagaiShin-ichi HashimotoShigenori NagaiMasahira HattoriTatsuro IrimuraDendritic cell (DC) subsets in the skin and draining lymph nodes (LNs) are likely to elicit distinct immune response types. In skin and skin-draining LNs, a dermal DC subset expressing macrophage galactose-type C-type lectin 2 (MGL2/CD301b) was found distinct from migratory Langerhans cells (LCs) or CD103(+) dermal DCs (dDCs). Lower expression levels of Th1-promoting and/or cross-presentation-related molecules were suggested by the transcriptome analysis and verified by the quantitative real-time PCR analysis in MGL2(+) dDCs than in CD103(+) dDCs. Transfer of MGL2(+) dDCs but not CD103(+) dDCs from FITC-sensitized mice induced a Th2-type immune response in vivo in a model of contact hypersensitivity. Targeting MGL2(+) dDCs with a rat monoclonal antibody against MGL2 efficiently induced a humoral immune response with Th2-type properties, as determined by the antibody subclass. We propose that the properties of MGL2(+) dDCs, are complementary to those of CD103(+) dDCs and skew the immune response toward a Th2-type response.http://europepmc.org/articles/PMC3767795?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ryuichi Murakami
Kaori Denda-Nagai
Shin-ichi Hashimoto
Shigenori Nagai
Masahira Hattori
Tatsuro Irimura
spellingShingle Ryuichi Murakami
Kaori Denda-Nagai
Shin-ichi Hashimoto
Shigenori Nagai
Masahira Hattori
Tatsuro Irimura
A unique dermal dendritic cell subset that skews the immune response toward Th2.
PLoS ONE
author_facet Ryuichi Murakami
Kaori Denda-Nagai
Shin-ichi Hashimoto
Shigenori Nagai
Masahira Hattori
Tatsuro Irimura
author_sort Ryuichi Murakami
title A unique dermal dendritic cell subset that skews the immune response toward Th2.
title_short A unique dermal dendritic cell subset that skews the immune response toward Th2.
title_full A unique dermal dendritic cell subset that skews the immune response toward Th2.
title_fullStr A unique dermal dendritic cell subset that skews the immune response toward Th2.
title_full_unstemmed A unique dermal dendritic cell subset that skews the immune response toward Th2.
title_sort unique dermal dendritic cell subset that skews the immune response toward th2.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Dendritic cell (DC) subsets in the skin and draining lymph nodes (LNs) are likely to elicit distinct immune response types. In skin and skin-draining LNs, a dermal DC subset expressing macrophage galactose-type C-type lectin 2 (MGL2/CD301b) was found distinct from migratory Langerhans cells (LCs) or CD103(+) dermal DCs (dDCs). Lower expression levels of Th1-promoting and/or cross-presentation-related molecules were suggested by the transcriptome analysis and verified by the quantitative real-time PCR analysis in MGL2(+) dDCs than in CD103(+) dDCs. Transfer of MGL2(+) dDCs but not CD103(+) dDCs from FITC-sensitized mice induced a Th2-type immune response in vivo in a model of contact hypersensitivity. Targeting MGL2(+) dDCs with a rat monoclonal antibody against MGL2 efficiently induced a humoral immune response with Th2-type properties, as determined by the antibody subclass. We propose that the properties of MGL2(+) dDCs, are complementary to those of CD103(+) dDCs and skew the immune response toward a Th2-type response.
url http://europepmc.org/articles/PMC3767795?pdf=render
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