Frailty in Old Age Is Associated with Decreased Interleukin-12/23 Production in Response to Toll-Like Receptor Ligation
Aging is associated with progressive alterations of immune functions, leading to higher susceptibility to bacterial and viral infections and reduced vaccine responses. Data concerning cytokine production in response to Toll-like receptor (TLR) ligands are highly variable in old people, reflecting th...
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Published in | PloS one Vol. 8; no. 6; p. e65325 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Public Library of Science
05.06.2013
Public Library of Science (PLoS) |
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Abstract | Aging is associated with progressive alterations of immune functions, leading to higher susceptibility to bacterial and viral infections and reduced vaccine responses. Data concerning cytokine production in response to Toll-like receptor (TLR) ligands are highly variable in old people, reflecting the heterogeneity of the geriatric population. The aim of our study was to define the relative contribution of age and clinical status on TLR-induced interleukin (IL)-12p70 and IL-23 production as these cytokines play an important role in the protection against intracellular and extracellular pathogens, respectively. For this purpose, we recruited 100 subjects (aged 23-96 years) in the general population or hospitalized for chronic diseases. We collected information on clinical status (medical history, ongoing comorbidities, treatments and geriatric scales), biological parameters (biochemical and hematological tests, telomere length determination, cytomegalovirus serology). Whole blood samples were stimulated with a combination of TLR4 and TLR7/8 ligands. We performed univariate and stepwise backward multivariate analyses regression to define which set of clinical variables could be predictive for IL-12p70 and IL-23 production in these conditions. Our results indicated that age was not correlated with TLR-mediated IL-12p70 and IL-23 production. In contrast, poor nutritional status and frailty in subjects >75 years were associated with decreased IL-12p70 and IL-23 production. By intracytoplasmic staining, we confirmed that production of IL-12/23p40 by conventional dendritic cells (DCs) upon TLR ligation was decreased in frail patients. However, proportion of DCs and monocytes subsets, phenotypic maturation and proximal signaling events were found to be comparable in frail and healthy old subjects. These results suggest the importance of age-associated clinical parameters and not age by itself in the alteration of innate immune responses in old individuals and emphasis the importance of innate immune responses in the susceptibility of frail geriatric patients to infections. |
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AbstractList | Aging is associated with progressive alterations of immune functions, leading to higher susceptibility to bacterial and viral infections and reduced vaccine responses. Data concerning cytokine production in response to Toll-like receptor (TLR) ligands are highly variable in old people, reflecting the heterogeneity of the geriatric population. The aim of our study was to define the relative contribution of age and clinical status on TLR-induced interleukin (IL)-12p70 and IL-23 production as these cytokines play an important role in the protection against intracellular and extracellular pathogens, respectively. For this purpose, we recruited 100 subjects (aged 23-96 years) in the general population or hospitalized for chronic diseases. We collected information on clinical status (medical history, ongoing comorbidities, treatments and geriatric scales), biological parameters (biochemical and hematological tests, telomere length determination, cytomegalovirus serology). Whole blood samples were stimulated with a combination of TLR4 and TLR7/8 ligands. We performed univariate and stepwise backward multivariate analyses regression to define which set of clinical variables could be predictive for IL-12p70 and IL-23 production in these conditions. Our results indicated that age was not correlated with TLR-mediated IL-12p70 and IL-23 production. In contrast, poor nutritional status and frailty in subjects >75 years were associated with decreased IL-12p70 and IL-23 production. By intracytoplasmic staining, we confirmed that production of IL-12/23p40 by conventional dendritic cells (DCs) upon TLR ligation was decreased in frail patients. However, proportion of DCs and monocytes subsets, phenotypic maturation and proximal signaling events were found to be comparable in frail and healthy old subjects. These results suggest the importance of age-associated clinical parameters and not age by itself in the alteration of innate immune responses in old individuals and emphasis the importance of innate immune responses in the susceptibility of frail geriatric patients to infections.Aging is associated with progressive alterations of immune functions, leading to higher susceptibility to bacterial and viral infections and reduced vaccine responses. Data concerning cytokine production in response to Toll-like receptor (TLR) ligands are highly variable in old people, reflecting the heterogeneity of the geriatric population. The aim of our study was to define the relative contribution of age and clinical status on TLR-induced interleukin (IL)-12p70 and IL-23 production as these cytokines play an important role in the protection against intracellular and extracellular pathogens, respectively. For this purpose, we recruited 100 subjects (aged 23-96 years) in the general population or hospitalized for chronic diseases. We collected information on clinical status (medical history, ongoing comorbidities, treatments and geriatric scales), biological parameters (biochemical and hematological tests, telomere length determination, cytomegalovirus serology). Whole blood samples were stimulated with a combination of TLR4 and TLR7/8 ligands. We performed univariate and stepwise backward multivariate analyses regression to define which set of clinical variables could be predictive for IL-12p70 and IL-23 production in these conditions. Our results indicated that age was not correlated with TLR-mediated IL-12p70 and IL-23 production. In contrast, poor nutritional status and frailty in subjects >75 years were associated with decreased IL-12p70 and IL-23 production. By intracytoplasmic staining, we confirmed that production of IL-12/23p40 by conventional dendritic cells (DCs) upon TLR ligation was decreased in frail patients. However, proportion of DCs and monocytes subsets, phenotypic maturation and proximal signaling events were found to be comparable in frail and healthy old subjects. These results suggest the importance of age-associated clinical parameters and not age by itself in the alteration of innate immune responses in old individuals and emphasis the importance of innate immune responses in the susceptibility of frail geriatric patients to infections. Aging is associated with progressive alterations of immune functions, leading to higher susceptibility to bacterial and viral infections and reduced vaccine responses. Data concerning cytokine production in response to Toll-like receptor (TLR) ligands are highly variable in old people, reflecting the heterogeneity of the geriatric population. The aim of our study was to define the relative contribution of age and clinical status on TLR-induced interleukin (IL)-12p70 and IL-23 production as these cytokines play an important role in the protection against intracellular and extracellular pathogens, respectively. For this purpose, we recruited 100 subjects (aged 23-96 years) in the general population or hospitalized for chronic diseases. We collected information on clinical status (medical history, ongoing comorbidities, treatments and geriatric scales), biological parameters (biochemical and hematological tests, telomere length determination, cytomegalovirus serology). Whole blood samples were stimulated with a combination of TLR4 and TLR7/8 ligands. We performed univariate and stepwise backward multivariate analyses regression to define which set of clinical variables could be predictive for IL-12p70 and IL-23 production in these conditions. Our results indicated that age was not correlated with TLR-mediated IL-12p70 and IL-23 production. In contrast, poor nutritional status and frailty in subjects >75 years were associated with decreased IL-12p70 and IL-23 production. By intracytoplasmic staining, we confirmed that production of IL-12/23p40 by conventional dendritic cells (DCs) upon TLR ligation was decreased in frail patients. However, proportion of DCs and monocytes subsets, phenotypic maturation and proximal signaling events were found to be comparable in frail and healthy old subjects. These results suggest the importance of age-associated clinical parameters and not age by itself in the alteration of innate immune responses in old individuals and emphasis the importance of innate immune responses in the susceptibility of frail geriatric patients to infections. |
Audience | Academic |
Author | Compté, Nathalie Zouaoui Boudjeltia, Karim Pepersack, Thierry Vanhaeverbeek, Michel De Breucker, Sandra Trelcat, Anne Tassignon, Joel Goriely, Stanislas |
AuthorAffiliation | University of Medicine and Dentistry of New Jersey - New Jersey Medical School, United States of America 3 Service de gériatrie, Hôpital Erasme, Bruxelles, Belgium 2 Experimental Medicine Laboratory (Unit 222), Université Libre de Bruxelles, Hôpital A. Vésale, Montigny-Le-Tilleul, Belgium 4 ImmuneHealth, Charleroi, Belgium 1 Institute for Medical Immunology (IMI), Université Libre de Bruxelles, Charleroi, Belgium |
AuthorAffiliation_xml | – name: 3 Service de gériatrie, Hôpital Erasme, Bruxelles, Belgium – name: University of Medicine and Dentistry of New Jersey - New Jersey Medical School, United States of America – name: 2 Experimental Medicine Laboratory (Unit 222), Université Libre de Bruxelles, Hôpital A. Vésale, Montigny-Le-Tilleul, Belgium – name: 1 Institute for Medical Immunology (IMI), Université Libre de Bruxelles, Charleroi, Belgium – name: 4 ImmuneHealth, Charleroi, Belgium |
Author_xml | – sequence: 1 givenname: Nathalie surname: Compté fullname: Compté, Nathalie – sequence: 2 givenname: Karim surname: Zouaoui Boudjeltia fullname: Zouaoui Boudjeltia, Karim – sequence: 3 givenname: Michel surname: Vanhaeverbeek fullname: Vanhaeverbeek, Michel – sequence: 4 givenname: Sandra surname: De Breucker fullname: De Breucker, Sandra – sequence: 5 givenname: Joel surname: Tassignon fullname: Tassignon, Joel – sequence: 6 givenname: Anne surname: Trelcat fullname: Trelcat, Anne – sequence: 7 givenname: Thierry surname: Pepersack fullname: Pepersack, Thierry – sequence: 8 givenname: Stanislas surname: Goriely fullname: Goriely, Stanislas |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23755218$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2013 Public Library of Science 2013 Compté et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2013 Compté et al 2013 Compté et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Competing Interests: The work was partly supported by a commercial source (GlaxoSmithKline Biologicals) and two authors are employed by a non-profit company (ImmuneHealth, Charleroi, Belgium). This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials. Conceived and designed the experiments: NC MV SG JT TP. Performed the experiments: NC AT. Analyzed the data: NC KZB TP. Contributed reagents/materials/analysis tools: SD. Wrote the paper: NC SG TP MV. |
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SubjectTerms | Activities of daily living Adult Age Aged Aged, 80 and over Aging Analysis Bacteria Blood & organ donations Cells, Cultured Chronic diseases Chronic illnesses Comorbidity Cytokines Cytomegalovirus Dendritic cells Dendritic Cells - immunology Dendritic Cells - metabolism Disease susceptibility Family medical history Female Frail Elderly Frailty Geriatrics Health aspects Health care Hematology Heterogeneity Hospitals Humans Imidazoles - pharmacology Immune response Immune system Immunity, Innate Immunology Infections Influenza Innate immunity Intercellular Adhesion Molecule-1 - metabolism Interleukin 12 Interleukin 23 Interleukin-12 - biosynthesis Interleukin-23 - biosynthesis Interleukins Laboratories Ligands Lipopolysaccharides - pharmacology Male Medicine Middle Aged Monocytes Nosocomial infections Nutritional status Nutritional Status - immunology Older people Patients Production management Proteins Recruitment Regression analysis Rodents Serology Signal Transduction Signaling Telomeres TLR4 protein TLR7 protein Toll-like receptors Toll-Like Receptors - agonists Toll-Like Receptors - metabolism Type 2 diabetes Vaccines Viral infections Womens health Young Adult |
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Title | Frailty in Old Age Is Associated with Decreased Interleukin-12/23 Production in Response to Toll-Like Receptor Ligation |
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