Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipients

Immune characteristics distinguishing tolerant lung transplant recipients (LTR) from patients with Bronchiolitis obliterans syndrome (BOS) are largely unknown. We compared the effect of dendritic cells (DC) on T-cell activation in healthy LTR (non BOS) and in BOS patients. 30 Non BOS and 14 BOS reci...

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Main Authors: K. Botturi, Y. Lacoeuille, P. Thomas, M. Reynaud-Gaubert, A. Magnan
Format: Article
Language:English
Published: European Respiratory Society 2008-04-01
Series:European Respiratory Review
Online Access:http://err.ersjournals.com/cgi/content/full/17/107/51
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spelling doaj-edd21fd86f1040028054c99e369a31a12020-11-25T01:25:00ZengEuropean Respiratory SocietyEuropean Respiratory Review0905-91801600-06172008-04-01171075152Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipientsK. BotturiY. LacoeuilleP. ThomasM. Reynaud-GaubertA. MagnanImmune characteristics distinguishing tolerant lung transplant recipients (LTR) from patients with Bronchiolitis obliterans syndrome (BOS) are largely unknown. We compared the effect of dendritic cells (DC) on T-cell activation in healthy LTR (non BOS) and in BOS patients. 30 Non BOS and 14 BOS recipients were studied. Mature dendritic cells were derived from blood monocytes and co-cultured with autologous T cells at various ratios. T cell CD69, CD25, CD28, ICOS and CTLA-4 expression and IL-4, IL-13, IFN-, and IL-10 production were assessed by flow cytometry. Dendritic cell expression of surface markers and indoleamine 2,3 dioxygenase was also studied. Experiments were repeated in presence of P. aeruginosa or anti-CTLA-4 antibodies. In dendritic cell/LT co-cultures, T cell CD69, CD28 and ICOS decreased in non BOS (p<0.03). By contrast, CD4+CD25+high T regulatory cells (Treg), CTLA4 expression and IL-10 production increased (p<0.05). Il-13 and IL-4 decreased in non BOS only (p<0.03), whereas IFN- did not vary. The increase in dendritic cell/LT ratio induced a decrease in T-cell activation in non BOS, with inverse result in BOS. Compared to BOS, dendritic cells from non BOS displayed a down-modulation of CD83, CD80 and higher levels of IDO (p<0.05). Stimulation by P. aeruginosa did not remove tolerogenic effect of dendritic cells on non BOS T-cells. Finally, decreased Treg and expression of IL-10 were detected when adding anti-CTLA-4 in non BOS (p<0.05) but not in BOS. In contrast with BOS recipients, dendritic cells from non BOS induce a tolerant T cell phenotype, by using CD80/CD86-CTLA4 axis. http://err.ersjournals.com/cgi/content/full/17/107/51
collection DOAJ
language English
format Article
sources DOAJ
author K. Botturi
Y. Lacoeuille
P. Thomas
M. Reynaud-Gaubert
A. Magnan
spellingShingle K. Botturi
Y. Lacoeuille
P. Thomas
M. Reynaud-Gaubert
A. Magnan
Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipients
European Respiratory Review
author_facet K. Botturi
Y. Lacoeuille
P. Thomas
M. Reynaud-Gaubert
A. Magnan
author_sort K. Botturi
title Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipients
title_short Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipients
title_full Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipients
title_fullStr Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipients
title_full_unstemmed Dendritic cells commit T-cells to a tolerant phenotype in tolerant lung transplant recipients
title_sort dendritic cells commit t-cells to a tolerant phenotype in tolerant lung transplant recipients
publisher European Respiratory Society
series European Respiratory Review
issn 0905-9180
1600-0617
publishDate 2008-04-01
description Immune characteristics distinguishing tolerant lung transplant recipients (LTR) from patients with Bronchiolitis obliterans syndrome (BOS) are largely unknown. We compared the effect of dendritic cells (DC) on T-cell activation in healthy LTR (non BOS) and in BOS patients. 30 Non BOS and 14 BOS recipients were studied. Mature dendritic cells were derived from blood monocytes and co-cultured with autologous T cells at various ratios. T cell CD69, CD25, CD28, ICOS and CTLA-4 expression and IL-4, IL-13, IFN-, and IL-10 production were assessed by flow cytometry. Dendritic cell expression of surface markers and indoleamine 2,3 dioxygenase was also studied. Experiments were repeated in presence of P. aeruginosa or anti-CTLA-4 antibodies. In dendritic cell/LT co-cultures, T cell CD69, CD28 and ICOS decreased in non BOS (p<0.03). By contrast, CD4+CD25+high T regulatory cells (Treg), CTLA4 expression and IL-10 production increased (p<0.05). Il-13 and IL-4 decreased in non BOS only (p<0.03), whereas IFN- did not vary. The increase in dendritic cell/LT ratio induced a decrease in T-cell activation in non BOS, with inverse result in BOS. Compared to BOS, dendritic cells from non BOS displayed a down-modulation of CD83, CD80 and higher levels of IDO (p<0.05). Stimulation by P. aeruginosa did not remove tolerogenic effect of dendritic cells on non BOS T-cells. Finally, decreased Treg and expression of IL-10 were detected when adding anti-CTLA-4 in non BOS (p<0.05) but not in BOS. In contrast with BOS recipients, dendritic cells from non BOS induce a tolerant T cell phenotype, by using CD80/CD86-CTLA4 axis.
url http://err.ersjournals.com/cgi/content/full/17/107/51
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