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Defective Granuloma Formation in Elderly Infected Patients

Granulomas are compact structures formed in tissues by the immune system in response to aggressions. The in vitro formation of granulomas using circulating mononuclear cells is an innovative method to easily assess the immune response of patients. Monitoring the efficiency of mononuclear cells from...

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Autores principales: Daumas, Aurélie, Coiffard, Benjamin, Chartier, Céline, Ben amara, Amira, Alingrin, Julie, Villani, Patrick, Mege, Jean-Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201002/
https://www.ncbi.nlm.nih.gov/pubmed/32411623
http://dx.doi.org/10.3389/fcimb.2020.00189
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author Daumas, Aurélie
Coiffard, Benjamin
Chartier, Céline
Ben amara, Amira
Alingrin, Julie
Villani, Patrick
Mege, Jean-Louis
author_facet Daumas, Aurélie
Coiffard, Benjamin
Chartier, Céline
Ben amara, Amira
Alingrin, Julie
Villani, Patrick
Mege, Jean-Louis
author_sort Daumas, Aurélie
collection PubMed
description Granulomas are compact structures formed in tissues by the immune system in response to aggressions. The in vitro formation of granulomas using circulating mononuclear cells is an innovative method to easily assess the immune response of patients. Monitoring the efficiency of mononuclear cells from patients to form granulomas in vitro would help improve their therapeutic management. Circulating mononuclear cells from 23 elderly patients with sepsis and 24 elderly controls patients were incubated with Sepharose beads coated with either BCG or Coxiella burnetii extracts. The formation of granulomas was measured over 9 days. Most healthy elderly patients (92%) were able to form granulomas in response to BCG and Coxiella burnetii extracts compared to only 48% of infected elderly patients. Undernutrition was significantly associated with impaired granuloma formation in healthy and infected patients. Granulomas typically comprise epithelioid cells and multinucleated giant cells, however, these cells were not detected in samples obtained from patients unable to form granulomas. We also found that the impairment of granuloma formation was associated with reduced production of tumor necrosis factor without overproduction of interleukin-10. Finally, all genes specifically modulated in granulomatous cells were down-modulated in patients with defective granuloma formation. TNFSF10 was the only M1 gene markedly upregulated in patients who did not form granulomas. Our study suggest that defective granuloma formation may be a measurement of altered activation of immune cells which can predispose to nosocomial infections in elderly patients.
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spelling pubmed-72010022020-05-14 Defective Granuloma Formation in Elderly Infected Patients Daumas, Aurélie Coiffard, Benjamin Chartier, Céline Ben amara, Amira Alingrin, Julie Villani, Patrick Mege, Jean-Louis Front Cell Infect Microbiol Cellular and Infection Microbiology Granulomas are compact structures formed in tissues by the immune system in response to aggressions. The in vitro formation of granulomas using circulating mononuclear cells is an innovative method to easily assess the immune response of patients. Monitoring the efficiency of mononuclear cells from patients to form granulomas in vitro would help improve their therapeutic management. Circulating mononuclear cells from 23 elderly patients with sepsis and 24 elderly controls patients were incubated with Sepharose beads coated with either BCG or Coxiella burnetii extracts. The formation of granulomas was measured over 9 days. Most healthy elderly patients (92%) were able to form granulomas in response to BCG and Coxiella burnetii extracts compared to only 48% of infected elderly patients. Undernutrition was significantly associated with impaired granuloma formation in healthy and infected patients. Granulomas typically comprise epithelioid cells and multinucleated giant cells, however, these cells were not detected in samples obtained from patients unable to form granulomas. We also found that the impairment of granuloma formation was associated with reduced production of tumor necrosis factor without overproduction of interleukin-10. Finally, all genes specifically modulated in granulomatous cells were down-modulated in patients with defective granuloma formation. TNFSF10 was the only M1 gene markedly upregulated in patients who did not form granulomas. Our study suggest that defective granuloma formation may be a measurement of altered activation of immune cells which can predispose to nosocomial infections in elderly patients. Frontiers Media S.A. 2020-04-29 /pmc/articles/PMC7201002/ /pubmed/32411623 http://dx.doi.org/10.3389/fcimb.2020.00189 Text en Copyright © 2020 Daumas, Coiffard, Chartier, Ben amara, Alingrin, Villani and Mege. http://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 Cellular and Infection Microbiology
Daumas, Aurélie
Coiffard, Benjamin
Chartier, Céline
Ben amara, Amira
Alingrin, Julie
Villani, Patrick
Mege, Jean-Louis
Defective Granuloma Formation in Elderly Infected Patients
title Defective Granuloma Formation in Elderly Infected Patients
title_full Defective Granuloma Formation in Elderly Infected Patients
title_fullStr Defective Granuloma Formation in Elderly Infected Patients
title_full_unstemmed Defective Granuloma Formation in Elderly Infected Patients
title_short Defective Granuloma Formation in Elderly Infected Patients
title_sort defective granuloma formation in elderly infected patients
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201002/
https://www.ncbi.nlm.nih.gov/pubmed/32411623
http://dx.doi.org/10.3389/fcimb.2020.00189
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