Cargando…

Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae

Chlamydophila pneumoniae (CPn) is a common respiratory pathogen that causes a chronic and persistent airway infection. The elderly display an increased susceptibility and severity to this infection. However, the underlying mechanisms are not well understood. Dendritic cells (DCs) are the initiators...

Descripción completa

Detalles Bibliográficos
Autores principales: Prakash, Sangeetha, Agrawal, Sudhanshu, Ma, Dandan, Gupta, Sudhir, Peterson, Ellena M., Agrawal, Anshu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165882/
https://www.ncbi.nlm.nih.gov/pubmed/25253920
http://dx.doi.org/10.1155/2014/436438
_version_ 1782335154269716480
author Prakash, Sangeetha
Agrawal, Sudhanshu
Ma, Dandan
Gupta, Sudhir
Peterson, Ellena M.
Agrawal, Anshu
author_facet Prakash, Sangeetha
Agrawal, Sudhanshu
Ma, Dandan
Gupta, Sudhir
Peterson, Ellena M.
Agrawal, Anshu
author_sort Prakash, Sangeetha
collection PubMed
description Chlamydophila pneumoniae (CPn) is a common respiratory pathogen that causes a chronic and persistent airway infection. The elderly display an increased susceptibility and severity to this infection. However, the underlying mechanisms are not well understood. Dendritic cells (DCs) are the initiators and regulators of immune responses. Therefore, we investigated the role of DCs in the age-associated increased CPn infection in vitro in humans. Though the expression of activation markers was comparable between the two age groups, DCs from aged subjects secreted enhanced levels of proinflammatory mediators such as TNF-α and CXCL-10 in response to CPn. In contrast, the secretion of IL-10 and innate interferons, IFN-α and IFN-λ, was severely impaired in DCs from aged donors. The increased activation of DCs from aged subjects to CPn also resulted in enhanced proliferation of CD4 and CD8 T cells in a DC-T coculture. Furthermore, T cells primed with CPn-stimulated DCs from aged subjects secreted increased levels of IFN-γ and reduced levels of IL-10 compared to DCs obtained from young subjects. In summary, DCs from the elderly displayed enhanced inflammatory response to CPn which may result in airway remodeling and increase the susceptibility of the elderly to respiratory diseases such as asthma.
format Online
Article
Text
id pubmed-4165882
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-41658822014-09-24 Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae Prakash, Sangeetha Agrawal, Sudhanshu Ma, Dandan Gupta, Sudhir Peterson, Ellena M. Agrawal, Anshu Mediators Inflamm Research Article Chlamydophila pneumoniae (CPn) is a common respiratory pathogen that causes a chronic and persistent airway infection. The elderly display an increased susceptibility and severity to this infection. However, the underlying mechanisms are not well understood. Dendritic cells (DCs) are the initiators and regulators of immune responses. Therefore, we investigated the role of DCs in the age-associated increased CPn infection in vitro in humans. Though the expression of activation markers was comparable between the two age groups, DCs from aged subjects secreted enhanced levels of proinflammatory mediators such as TNF-α and CXCL-10 in response to CPn. In contrast, the secretion of IL-10 and innate interferons, IFN-α and IFN-λ, was severely impaired in DCs from aged donors. The increased activation of DCs from aged subjects to CPn also resulted in enhanced proliferation of CD4 and CD8 T cells in a DC-T coculture. Furthermore, T cells primed with CPn-stimulated DCs from aged subjects secreted increased levels of IFN-γ and reduced levels of IL-10 compared to DCs obtained from young subjects. In summary, DCs from the elderly displayed enhanced inflammatory response to CPn which may result in airway remodeling and increase the susceptibility of the elderly to respiratory diseases such as asthma. Hindawi Publishing Corporation 2014 2014-09-01 /pmc/articles/PMC4165882/ /pubmed/25253920 http://dx.doi.org/10.1155/2014/436438 Text en Copyright © 2014 Sangeetha Prakash et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Prakash, Sangeetha
Agrawal, Sudhanshu
Ma, Dandan
Gupta, Sudhir
Peterson, Ellena M.
Agrawal, Anshu
Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae
title Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae
title_full Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae
title_fullStr Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae
title_full_unstemmed Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae
title_short Dendritic Cells from Aged Subjects Display Enhanced Inflammatory Responses to Chlamydophila pneumoniae
title_sort dendritic cells from aged subjects display enhanced inflammatory responses to chlamydophila pneumoniae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165882/
https://www.ncbi.nlm.nih.gov/pubmed/25253920
http://dx.doi.org/10.1155/2014/436438
work_keys_str_mv AT prakashsangeetha dendriticcellsfromagedsubjectsdisplayenhancedinflammatoryresponsestochlamydophilapneumoniae
AT agrawalsudhanshu dendriticcellsfromagedsubjectsdisplayenhancedinflammatoryresponsestochlamydophilapneumoniae
AT madandan dendriticcellsfromagedsubjectsdisplayenhancedinflammatoryresponsestochlamydophilapneumoniae
AT guptasudhir dendriticcellsfromagedsubjectsdisplayenhancedinflammatoryresponsestochlamydophilapneumoniae
AT petersonellenam dendriticcellsfromagedsubjectsdisplayenhancedinflammatoryresponsestochlamydophilapneumoniae
AT agrawalanshu dendriticcellsfromagedsubjectsdisplayenhancedinflammatoryresponsestochlamydophilapneumoniae