Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.

A crucial step in generating de novo immune responses is the polarization of naive cognate CD4+ T cells by pathogen-triggered dendritic cells (DC). In the human setting, standardized DC-dependent systems are lacking to study molecular events during the initiation of a naive CD4+ T cell response. We...

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Main Authors: Tammy Oth, Melanie C A Schnijderberg, Birgit L M G Senden-Gijsbers, Wilfred T V Germeraad, Gerard M J Bos, Joris Vanderlocht
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4140687?pdf=render
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spelling doaj-097864381b9a409aa213b6c43a060f262020-11-25T02:29:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0198e10372510.1371/journal.pone.0103725Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.Tammy OthMelanie C A SchnijderbergBirgit L M G Senden-GijsbersWilfred T V GermeraadGerard M J BosJoris VanderlochtA crucial step in generating de novo immune responses is the polarization of naive cognate CD4+ T cells by pathogen-triggered dendritic cells (DC). In the human setting, standardized DC-dependent systems are lacking to study molecular events during the initiation of a naive CD4+ T cell response. We developed a TCR-restricted assay to compare different pathogen-triggered human DC for their capacities to instruct functional differentiation of autologous, naive CD4+ T cells. We demonstrated that this methodology can be applied to compare differently matured DC in terms of kinetics, direction, and magnitude of the naive CD4+ T cell response. Furthermore, we showed the applicability of this assay to study the T cell polarizing capacity of low-frequency blood-derived DC populations directly isolated ex vivo. This methodology for addressing APC-dependent instruction of naive CD4+ T cells in a human autologous setting will provide researchers with a valuable tool to gain more insight into molecular mechanisms occurring in the early phase of T cell polarization. In addition, it may also allow the study of pharmacological agents on DC-dependent T cell polarization in the human system.http://europepmc.org/articles/PMC4140687?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Tammy Oth
Melanie C A Schnijderberg
Birgit L M G Senden-Gijsbers
Wilfred T V Germeraad
Gerard M J Bos
Joris Vanderlocht
spellingShingle Tammy Oth
Melanie C A Schnijderberg
Birgit L M G Senden-Gijsbers
Wilfred T V Germeraad
Gerard M J Bos
Joris Vanderlocht
Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.
PLoS ONE
author_facet Tammy Oth
Melanie C A Schnijderberg
Birgit L M G Senden-Gijsbers
Wilfred T V Germeraad
Gerard M J Bos
Joris Vanderlocht
author_sort Tammy Oth
title Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.
title_short Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.
title_full Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.
title_fullStr Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.
title_full_unstemmed Monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive CD4+ T cells.
title_sort monitoring the initiation and kinetics of human dendritic cell-induced polarization of autologous naive cd4+ t cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description A crucial step in generating de novo immune responses is the polarization of naive cognate CD4+ T cells by pathogen-triggered dendritic cells (DC). In the human setting, standardized DC-dependent systems are lacking to study molecular events during the initiation of a naive CD4+ T cell response. We developed a TCR-restricted assay to compare different pathogen-triggered human DC for their capacities to instruct functional differentiation of autologous, naive CD4+ T cells. We demonstrated that this methodology can be applied to compare differently matured DC in terms of kinetics, direction, and magnitude of the naive CD4+ T cell response. Furthermore, we showed the applicability of this assay to study the T cell polarizing capacity of low-frequency blood-derived DC populations directly isolated ex vivo. This methodology for addressing APC-dependent instruction of naive CD4+ T cells in a human autologous setting will provide researchers with a valuable tool to gain more insight into molecular mechanisms occurring in the early phase of T cell polarization. In addition, it may also allow the study of pharmacological agents on DC-dependent T cell polarization in the human system.
url http://europepmc.org/articles/PMC4140687?pdf=render
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