Cargando…

The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study

RATIONALE: To prevent or combat infection, increasing the effectiveness of the immune response is highly desirable, especially in case of compromised immune system function. However, immunostimulatory therapies are scarce, expensive, and often have unwanted side-effects. β-glucans have been shown to...

Descripción completa

Detalles Bibliográficos
Autores principales: Leentjens, Jenneke, Quintin, Jessica, Gerretsen, Jelle, Kox, Matthijs, Pickkers, Peter, Netea, Mihai G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182605/
https://www.ncbi.nlm.nih.gov/pubmed/25268806
http://dx.doi.org/10.1371/journal.pone.0108794
_version_ 1782337565856104448
author Leentjens, Jenneke
Quintin, Jessica
Gerretsen, Jelle
Kox, Matthijs
Pickkers, Peter
Netea, Mihai G.
author_facet Leentjens, Jenneke
Quintin, Jessica
Gerretsen, Jelle
Kox, Matthijs
Pickkers, Peter
Netea, Mihai G.
author_sort Leentjens, Jenneke
collection PubMed
description RATIONALE: To prevent or combat infection, increasing the effectiveness of the immune response is highly desirable, especially in case of compromised immune system function. However, immunostimulatory therapies are scarce, expensive, and often have unwanted side-effects. β-glucans have been shown to exert immunostimulatory effects in vitro and in vivo in experimental animal models. Oral β-glucan is inexpensive and well-tolerated, and therefore may represent a promising immunostimulatory compound for human use. METHODS: We performed a randomized open-label intervention pilot-study in 15 healthy male volunteers. Subjects were randomized to either the β -glucan (n = 10) or the control group (n = 5). Subjects in the β-glucan group ingested β-glucan 1000 mg once daily for 7 days. Blood was sampled at various time-points to determine β-glucan serum levels, perform ex vivo stimulation of leukocytes, and analyze microbicidal activity. RESULTS: β-glucan was barely detectable in serum of volunteers at all time-points. Furthermore, neither cytokine production nor microbicidal activity of leukocytes were affected by orally administered β-glucan. CONCLUSION: The present study does not support the use of oral β-glucan to enhance innate immune responses in humans. TRIAL REGISTRATION: ClinicalTrials.gov NCT01727895
format Online
Article
Text
id pubmed-4182605
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-41826052014-10-07 The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study Leentjens, Jenneke Quintin, Jessica Gerretsen, Jelle Kox, Matthijs Pickkers, Peter Netea, Mihai G. PLoS One Research Article RATIONALE: To prevent or combat infection, increasing the effectiveness of the immune response is highly desirable, especially in case of compromised immune system function. However, immunostimulatory therapies are scarce, expensive, and often have unwanted side-effects. β-glucans have been shown to exert immunostimulatory effects in vitro and in vivo in experimental animal models. Oral β-glucan is inexpensive and well-tolerated, and therefore may represent a promising immunostimulatory compound for human use. METHODS: We performed a randomized open-label intervention pilot-study in 15 healthy male volunteers. Subjects were randomized to either the β -glucan (n = 10) or the control group (n = 5). Subjects in the β-glucan group ingested β-glucan 1000 mg once daily for 7 days. Blood was sampled at various time-points to determine β-glucan serum levels, perform ex vivo stimulation of leukocytes, and analyze microbicidal activity. RESULTS: β-glucan was barely detectable in serum of volunteers at all time-points. Furthermore, neither cytokine production nor microbicidal activity of leukocytes were affected by orally administered β-glucan. CONCLUSION: The present study does not support the use of oral β-glucan to enhance innate immune responses in humans. TRIAL REGISTRATION: ClinicalTrials.gov NCT01727895 Public Library of Science 2014-09-30 /pmc/articles/PMC4182605/ /pubmed/25268806 http://dx.doi.org/10.1371/journal.pone.0108794 Text en © 2014 Leentjens et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Leentjens, Jenneke
Quintin, Jessica
Gerretsen, Jelle
Kox, Matthijs
Pickkers, Peter
Netea, Mihai G.
The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study
title The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study
title_full The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study
title_fullStr The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study
title_full_unstemmed The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study
title_short The Effects of Orally Administered Beta-Glucan on Innate Immune Responses in Humans, a Randomized Open-Label Intervention Pilot-Study
title_sort effects of orally administered beta-glucan on innate immune responses in humans, a randomized open-label intervention pilot-study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182605/
https://www.ncbi.nlm.nih.gov/pubmed/25268806
http://dx.doi.org/10.1371/journal.pone.0108794
work_keys_str_mv AT leentjensjenneke theeffectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT quintinjessica theeffectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT gerretsenjelle theeffectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT koxmatthijs theeffectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT pickkerspeter theeffectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT neteamihaig theeffectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT leentjensjenneke effectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT quintinjessica effectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT gerretsenjelle effectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT koxmatthijs effectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT pickkerspeter effectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy
AT neteamihaig effectsoforallyadministeredbetaglucanoninnateimmuneresponsesinhumansarandomizedopenlabelinterventionpilotstudy