Literature DB >> 22333879

Plasmacytoid dendritic cells and Th17 immune response contribution in gastrointestinal acute graft-versus-host disease.

C Bossard1, F Malard, J Arbez, P Chevallier, T Guillaume, J Delaunay, J-F Mosnier, P Tiberghien, P Saas, M Mohty, B Gaugler.   

Abstract

The contribution of Th17 cells in acute graft-versus-host disease (aGVHD) has been demonstrated in aGVHD mouse models. However, their contribution in human gastrointestinal aGVHD remains unclear. We evaluated Th17 cells in a cohort of 23 patients at diagnosis of aGVHD. In this study, we have shown that the absolute number of Th17 cells using the CCR6 and CD161 markers were significantly higher in the intestinal mucosa of patients with aGVHD compared with intestinal mucosa of patients without aGVHD. Moreover, in keeping with the increase of CCR6+ and CD161+ T cells, RORγt the key transcription factor that orchestrates the differentiation of Th17 cells, was significantly increased in the intestinal mucosa of patients with aGVHD compared with intestinal mucosa of patients without aGVHD (P=0.01). Since plasmacytoid dendritic cells (PDCs) have been reported to drive the differentiation of the Th17 subset, we quantified PDCs in these patients. PDC CD123+ cells were increased in the intestinal mucosa of patients with aGVHD. Furthermore, the number of CD123+ PDCs paralleled the histological grade of aGVHD, providing evidence for a role of Th17-mediated responses and a potential new pathophysiological link between PDCs and Th17 in human aGVHD.

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Year:  2012        PMID: 22333879     DOI: 10.1038/leu.2012.41

Source DB:  PubMed          Journal:  Leukemia        ISSN: 0887-6924            Impact factor:   11.528


  21 in total

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4.  The Notch Ligand DLL4 Defines a Capability of Human Dendritic Cells in Regulating Th1 and Th17 Differentiation.

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5.  Proteomics analysis reveals a Th17-prone cell population in presymptomatic graft-versus-host disease.

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Review 8.  Translational opportunities for targeting the Th17 axis in acute graft-vs.-host disease.

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Journal:  Mucosal Immunol       Date:  2016-01-27       Impact factor: 7.313

9.  Rejection of intestinal allotransplants is driven by memory T helper type 17 immunity and responds to infliximab.

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10.  Tolerogenic and activatory plasmacytoid dendritic cells in autoimmunity.

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Journal:  Front Immunol       Date:  2013-03-06       Impact factor: 7.561

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