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The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status

HLA-B27 is the allele most frequently associated with human anterior uveitis. The majority of HLA-B27-positive [acute anterior uveitis (AAU)] patients develop clinically distinct symptoms with acute symptomatic onset of flare and a recurrent disease course characterized by a massive cellular ocular...

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Autores principales: Kasper, Maren, Walscheid, Karoline, Laffer, Björn, Bauer, Dirk, Busch, Martin, Wildschütz, Lena, Wang, Bo, Loser, Karin, Vogl, Thomas, Grajewski, Rafael S., Langmann, Thomas, Heiligenhaus, Arnd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077321/
https://www.ncbi.nlm.nih.gov/pubmed/30105034
http://dx.doi.org/10.3389/fimmu.2018.01773
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author Kasper, Maren
Walscheid, Karoline
Laffer, Björn
Bauer, Dirk
Busch, Martin
Wildschütz, Lena
Wang, Bo
Loser, Karin
Vogl, Thomas
Grajewski, Rafael S.
Langmann, Thomas
Heiligenhaus, Arnd
author_facet Kasper, Maren
Walscheid, Karoline
Laffer, Björn
Bauer, Dirk
Busch, Martin
Wildschütz, Lena
Wang, Bo
Loser, Karin
Vogl, Thomas
Grajewski, Rafael S.
Langmann, Thomas
Heiligenhaus, Arnd
author_sort Kasper, Maren
collection PubMed
description HLA-B27 is the allele most frequently associated with human anterior uveitis. The majority of HLA-B27-positive [acute anterior uveitis (AAU)] patients develop clinically distinct symptoms with acute symptomatic onset of flare and a recurrent disease course characterized by a massive cellular ocular infiltrate during uveitis relapse. By contrast, uveitis in HLA-B27-negative [idiopathic anterior uveitis (IAU)] patients tends to develop a clinically less fulminant, more chronic, and typically asymptomatic disease course. To analyze systemic immune responses in the different uveitis entities, we analyzed peripheral blood cells by flow cytometry. In addition, as a pro-inflammatory biomarker serum, S100A8/A9 levels were quantified by ELISA from patients with AAU (n = 27) and IAU (n = 21), and in healthy controls (n = 30). Data were obtained either during active uveitis flare or after 3 months of inactivity. IAU patients showed a transiently increased frequency of CD56- and CD163-positive monocytes and of both granulocytic myeloid-derived suppressor cells and Th17 cells during active uveitis. By contrast, AAU patients showed an elevated frequency of monocytes, activated T cells, and elevated S100A8/A9 serum levels during clinically quiescent disease. The differentially regulated response of both innate and adaptive immune cells in the blood may be related to the clinically distinct characteristics of the two different uveitis entities.
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spelling pubmed-60773212018-08-13 The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status Kasper, Maren Walscheid, Karoline Laffer, Björn Bauer, Dirk Busch, Martin Wildschütz, Lena Wang, Bo Loser, Karin Vogl, Thomas Grajewski, Rafael S. Langmann, Thomas Heiligenhaus, Arnd Front Immunol Immunology HLA-B27 is the allele most frequently associated with human anterior uveitis. The majority of HLA-B27-positive [acute anterior uveitis (AAU)] patients develop clinically distinct symptoms with acute symptomatic onset of flare and a recurrent disease course characterized by a massive cellular ocular infiltrate during uveitis relapse. By contrast, uveitis in HLA-B27-negative [idiopathic anterior uveitis (IAU)] patients tends to develop a clinically less fulminant, more chronic, and typically asymptomatic disease course. To analyze systemic immune responses in the different uveitis entities, we analyzed peripheral blood cells by flow cytometry. In addition, as a pro-inflammatory biomarker serum, S100A8/A9 levels were quantified by ELISA from patients with AAU (n = 27) and IAU (n = 21), and in healthy controls (n = 30). Data were obtained either during active uveitis flare or after 3 months of inactivity. IAU patients showed a transiently increased frequency of CD56- and CD163-positive monocytes and of both granulocytic myeloid-derived suppressor cells and Th17 cells during active uveitis. By contrast, AAU patients showed an elevated frequency of monocytes, activated T cells, and elevated S100A8/A9 serum levels during clinically quiescent disease. The differentially regulated response of both innate and adaptive immune cells in the blood may be related to the clinically distinct characteristics of the two different uveitis entities. Frontiers Media S.A. 2018-07-30 /pmc/articles/PMC6077321/ /pubmed/30105034 http://dx.doi.org/10.3389/fimmu.2018.01773 Text en Copyright © 2018 Kasper, Walscheid, Laffer, Bauer, Busch, Wildschütz, Wang, Loser, Vogl, Grajewski, Langmann and Heiligenhaus. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Kasper, Maren
Walscheid, Karoline
Laffer, Björn
Bauer, Dirk
Busch, Martin
Wildschütz, Lena
Wang, Bo
Loser, Karin
Vogl, Thomas
Grajewski, Rafael S.
Langmann, Thomas
Heiligenhaus, Arnd
The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status
title The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status
title_full The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status
title_fullStr The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status
title_full_unstemmed The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status
title_short The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 Status
title_sort phenotype of monocytes in anterior uveitis depends on the hla-b27 status
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077321/
https://www.ncbi.nlm.nih.gov/pubmed/30105034
http://dx.doi.org/10.3389/fimmu.2018.01773
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