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Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis

OBJECTIVES: The pathophysiological mechanisms of chronic rhinosinusitis with nasal polyposis (CRSwNP) still are discussed controversially. Regulatory B cells (B(reg)) are responsible for the suppression of T cell activity: deficiencies for B(reg) have been demonstrated to contribute to autoimmune di...

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Autores principales: Ickrath, Pascal, Kleinsasser, Norbert, Ding, Xin, Ginzkey, Christian, Beyersdorf, Niklas, Kerkau, Thomas, Hagen, Rudolf, Hackenberg, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Otorhinolaryngology-Head and Neck Surgery 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951070/
https://www.ncbi.nlm.nih.gov/pubmed/29409312
http://dx.doi.org/10.21053/ceo.2017.01389
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author Ickrath, Pascal
Kleinsasser, Norbert
Ding, Xin
Ginzkey, Christian
Beyersdorf, Niklas
Kerkau, Thomas
Hagen, Rudolf
Hackenberg, Stephan
author_facet Ickrath, Pascal
Kleinsasser, Norbert
Ding, Xin
Ginzkey, Christian
Beyersdorf, Niklas
Kerkau, Thomas
Hagen, Rudolf
Hackenberg, Stephan
author_sort Ickrath, Pascal
collection PubMed
description OBJECTIVES: The pathophysiological mechanisms of chronic rhinosinusitis with nasal polyposis (CRSwNP) still are discussed controversially. Regulatory B cells (B(reg)) are responsible for the suppression of T cell activity: deficiencies for B(reg) have been demonstrated to contribute to autoimmune disorders, e.g., systemic lupus erythematosus. In order to evaluate the influence of B cell subpopulations, especially B(reg), on the etiology of this disease, the aim of this study was to characterize subpopulations of peripheral and edaphic B cells in CRSwNP. METHODS: Polypoid tissue and blood samples were collected from 10 patients undergoing paranasal sinus surgery and lymphocytes were analyzed by multicolor flow cytometry. RESULTS: There was a significantly lower frequency of B cells in nasal polyps compared to peripheral blood mononuclear cells (PBMC) in patients with CRSwNP. Mature resting B cells were the main population within B cells in PBMC, and memory B cells in nasal polyps. Remarkably, B(reg) and mature B cells significantly decreased in nasal polyps compared to PBMC. Memory B cells significantly increased and represented the main subpopulation in nasal polyps in patients with CRSwNP. CONCLUSION: In this study a detailed contemporary characterization of B cell subpopulations in patients with CRSwNP is presented. The influence of edaphic B cells could play a key role in the maintenance of this chronic infectious disease.
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spelling pubmed-59510702018-06-01 Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis Ickrath, Pascal Kleinsasser, Norbert Ding, Xin Ginzkey, Christian Beyersdorf, Niklas Kerkau, Thomas Hagen, Rudolf Hackenberg, Stephan Clin Exp Otorhinolaryngol Original Article OBJECTIVES: The pathophysiological mechanisms of chronic rhinosinusitis with nasal polyposis (CRSwNP) still are discussed controversially. Regulatory B cells (B(reg)) are responsible for the suppression of T cell activity: deficiencies for B(reg) have been demonstrated to contribute to autoimmune disorders, e.g., systemic lupus erythematosus. In order to evaluate the influence of B cell subpopulations, especially B(reg), on the etiology of this disease, the aim of this study was to characterize subpopulations of peripheral and edaphic B cells in CRSwNP. METHODS: Polypoid tissue and blood samples were collected from 10 patients undergoing paranasal sinus surgery and lymphocytes were analyzed by multicolor flow cytometry. RESULTS: There was a significantly lower frequency of B cells in nasal polyps compared to peripheral blood mononuclear cells (PBMC) in patients with CRSwNP. Mature resting B cells were the main population within B cells in PBMC, and memory B cells in nasal polyps. Remarkably, B(reg) and mature B cells significantly decreased in nasal polyps compared to PBMC. Memory B cells significantly increased and represented the main subpopulation in nasal polyps in patients with CRSwNP. CONCLUSION: In this study a detailed contemporary characterization of B cell subpopulations in patients with CRSwNP is presented. The influence of edaphic B cells could play a key role in the maintenance of this chronic infectious disease. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2018-06 2018-02-08 /pmc/articles/PMC5951070/ /pubmed/29409312 http://dx.doi.org/10.21053/ceo.2017.01389 Text en Copyright © 2018 by Korean Society of Otorhinolaryngology-Head and Neck Surgery This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ickrath, Pascal
Kleinsasser, Norbert
Ding, Xin
Ginzkey, Christian
Beyersdorf, Niklas
Kerkau, Thomas
Hagen, Rudolf
Hackenberg, Stephan
Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis
title Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis
title_full Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis
title_fullStr Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis
title_full_unstemmed Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis
title_short Impact and Modulations of Peripheral and Edaphic B Cell Subpopulations in Chronic Rhinosinusitis With Nasal Polyposis
title_sort impact and modulations of peripheral and edaphic b cell subpopulations in chronic rhinosinusitis with nasal polyposis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951070/
https://www.ncbi.nlm.nih.gov/pubmed/29409312
http://dx.doi.org/10.21053/ceo.2017.01389
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