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The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms

BACKGROUND: The mechanisms underlying the non-antimicrobial immunomodulatory properties of macrolides are not well understood. OBJECTIVES: To systematically review the evidence for the immunomodulatory properties of macrolides in humans and to describe the underlying mechanism and extent of their in...

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Autores principales: Zimmermann, Petra, Ziesenitz, Victoria C., Curtis, Nigel, Ritz, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859047/
https://www.ncbi.nlm.nih.gov/pubmed/29593707
http://dx.doi.org/10.3389/fimmu.2018.00302
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author Zimmermann, Petra
Ziesenitz, Victoria C.
Curtis, Nigel
Ritz, Nicole
author_facet Zimmermann, Petra
Ziesenitz, Victoria C.
Curtis, Nigel
Ritz, Nicole
author_sort Zimmermann, Petra
collection PubMed
description BACKGROUND: The mechanisms underlying the non-antimicrobial immunomodulatory properties of macrolides are not well understood. OBJECTIVES: To systematically review the evidence for the immunomodulatory properties of macrolides in humans and to describe the underlying mechanism and extent of their influence on the innate and adaptive immune system. METHODS: A systematic literature search was done in MEDLINE using the OVID interface from 1946 to December 2016 according to the preferred reporting items for systematic reviews and meta-analysis (PRISMA). Original articles investigating the influence of four macrolides (azithromycin, clarithromycin, erythromycin, and roxithromycin) on immunological markers in humans were included. RESULTS: We identified 22 randomized, controlled trials, 16 prospective cohort studies, and 8 case–control studies investigating 47 different immunological markers (186 measurements) in 1,834 participants. The most frequently reported outcomes were a decrease in the number of neutrophils, and the concentrations of neutrophil elastase, interleukin (IL)-8, IL-6, IL-1beta, tumor necrosis factor (TNF)-alpha, eosinophilic cationic protein, and matrix metalloproteinase 9. Inhibition of neutrophil function was reported more frequently than eosinophil function. A decrease in T helper (Th) 2 cells cytokines (IL-4, IL-5, IL-6) was reported more frequently than a decrease in Th1 cytokines (IL-2, INF-gamma). CONCLUSION: Macrolides influence a broad range of immunological mechanisms resulting in immunomodulatory effects. To optimize the treatment of chronic inflammatory diseases by macrolides, further studies are necessary, particularly comparing different macrolides and dose effect relationships.
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spelling pubmed-58590472018-03-28 The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms Zimmermann, Petra Ziesenitz, Victoria C. Curtis, Nigel Ritz, Nicole Front Immunol Immunology BACKGROUND: The mechanisms underlying the non-antimicrobial immunomodulatory properties of macrolides are not well understood. OBJECTIVES: To systematically review the evidence for the immunomodulatory properties of macrolides in humans and to describe the underlying mechanism and extent of their influence on the innate and adaptive immune system. METHODS: A systematic literature search was done in MEDLINE using the OVID interface from 1946 to December 2016 according to the preferred reporting items for systematic reviews and meta-analysis (PRISMA). Original articles investigating the influence of four macrolides (azithromycin, clarithromycin, erythromycin, and roxithromycin) on immunological markers in humans were included. RESULTS: We identified 22 randomized, controlled trials, 16 prospective cohort studies, and 8 case–control studies investigating 47 different immunological markers (186 measurements) in 1,834 participants. The most frequently reported outcomes were a decrease in the number of neutrophils, and the concentrations of neutrophil elastase, interleukin (IL)-8, IL-6, IL-1beta, tumor necrosis factor (TNF)-alpha, eosinophilic cationic protein, and matrix metalloproteinase 9. Inhibition of neutrophil function was reported more frequently than eosinophil function. A decrease in T helper (Th) 2 cells cytokines (IL-4, IL-5, IL-6) was reported more frequently than a decrease in Th1 cytokines (IL-2, INF-gamma). CONCLUSION: Macrolides influence a broad range of immunological mechanisms resulting in immunomodulatory effects. To optimize the treatment of chronic inflammatory diseases by macrolides, further studies are necessary, particularly comparing different macrolides and dose effect relationships. Frontiers Media S.A. 2018-03-13 /pmc/articles/PMC5859047/ /pubmed/29593707 http://dx.doi.org/10.3389/fimmu.2018.00302 Text en Copyright © 2018 Zimmermann, Ziesenitz, Curtis and Ritz. 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 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 Immunology
Zimmermann, Petra
Ziesenitz, Victoria C.
Curtis, Nigel
Ritz, Nicole
The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms
title The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms
title_full The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms
title_fullStr The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms
title_full_unstemmed The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms
title_short The Immunomodulatory Effects of Macrolides—A Systematic Review of the Underlying Mechanisms
title_sort immunomodulatory effects of macrolides—a systematic review of the underlying mechanisms
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859047/
https://www.ncbi.nlm.nih.gov/pubmed/29593707
http://dx.doi.org/10.3389/fimmu.2018.00302
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