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IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients
BACKGROUND: Cytomegalovirus seropositivity is an independent risk factor for atherosclerosis in patients with ESRD. Donor CMV seropositivity is associated with higher graft loss. Dendritic cells, macrophages and Th17 lymphocytes are defined as producers of IL-23. IL-23 is thought to be involved in t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048605/ https://www.ncbi.nlm.nih.gov/pubmed/27716059 http://dx.doi.org/10.1186/s12865-016-0175-7 |
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author | Sadeghi, Mahmoud Lahdou, Imad Opelz, Gerhard Mehrabi, Arianeb Zeier, Martin Schnitzler, Paul Daniel, Volker |
author_facet | Sadeghi, Mahmoud Lahdou, Imad Opelz, Gerhard Mehrabi, Arianeb Zeier, Martin Schnitzler, Paul Daniel, Volker |
author_sort | Sadeghi, Mahmoud |
collection | PubMed |
description | BACKGROUND: Cytomegalovirus seropositivity is an independent risk factor for atherosclerosis in patients with ESRD. Donor CMV seropositivity is associated with higher graft loss. Dendritic cells, macrophages and Th17 lymphocytes are defined as producers of IL-23. IL-23 is thought to be involved in the promotion of Th17 cell polarization. Latent CMV-induced Th17 might be involved in the pathogenesis of CMV infection in patients with ESRD. We aimed to evaluate associations of Th17-dependent cytokines with ESRD, CMV status and post-transplant outcome in kidney transplantation. RESULTS: IL-21 plasma levels were similar in patients and healthy controls (p = 0.47), whereas IL-9 (p = 0.02) and IL-23 (p < 0.0001) levels were significantly higher in ESRD patients. CMV-seronegative (p = 0.002) and –seropositive (p < 0.001) patients had significantly higher IL-23 plasma levels than controls. CMV-seropositive patients showed excessively higher IL-23 (p < 0.001) plasma levels than CMV-seronegative patients. Patients with post-transplant CMV reactivation had higher IL-23 plasma levels than patients without CMV reactivation (p = 0.025). CONCLUSIONS: Our results indicate that latent CMV induces IL-23. IL-23 might be an inflammatory mediator of latent CMV infection in patients with ESRD and predisposes patients for post-transplant CMV reactivation. |
format | Online Article Text |
id | pubmed-5048605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50486052016-10-11 IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients Sadeghi, Mahmoud Lahdou, Imad Opelz, Gerhard Mehrabi, Arianeb Zeier, Martin Schnitzler, Paul Daniel, Volker BMC Immunol Research Article BACKGROUND: Cytomegalovirus seropositivity is an independent risk factor for atherosclerosis in patients with ESRD. Donor CMV seropositivity is associated with higher graft loss. Dendritic cells, macrophages and Th17 lymphocytes are defined as producers of IL-23. IL-23 is thought to be involved in the promotion of Th17 cell polarization. Latent CMV-induced Th17 might be involved in the pathogenesis of CMV infection in patients with ESRD. We aimed to evaluate associations of Th17-dependent cytokines with ESRD, CMV status and post-transplant outcome in kidney transplantation. RESULTS: IL-21 plasma levels were similar in patients and healthy controls (p = 0.47), whereas IL-9 (p = 0.02) and IL-23 (p < 0.0001) levels were significantly higher in ESRD patients. CMV-seronegative (p = 0.002) and –seropositive (p < 0.001) patients had significantly higher IL-23 plasma levels than controls. CMV-seropositive patients showed excessively higher IL-23 (p < 0.001) plasma levels than CMV-seronegative patients. Patients with post-transplant CMV reactivation had higher IL-23 plasma levels than patients without CMV reactivation (p = 0.025). CONCLUSIONS: Our results indicate that latent CMV induces IL-23. IL-23 might be an inflammatory mediator of latent CMV infection in patients with ESRD and predisposes patients for post-transplant CMV reactivation. BioMed Central 2016-10-03 /pmc/articles/PMC5048605/ /pubmed/27716059 http://dx.doi.org/10.1186/s12865-016-0175-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Sadeghi, Mahmoud Lahdou, Imad Opelz, Gerhard Mehrabi, Arianeb Zeier, Martin Schnitzler, Paul Daniel, Volker IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients |
title | IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients |
title_full | IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients |
title_fullStr | IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients |
title_full_unstemmed | IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients |
title_short | IL-23 plasma level is strongly associated with CMV status and reactivation of CMV in renal transplant recipients |
title_sort | il-23 plasma level is strongly associated with cmv status and reactivation of cmv in renal transplant recipients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048605/ https://www.ncbi.nlm.nih.gov/pubmed/27716059 http://dx.doi.org/10.1186/s12865-016-0175-7 |
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