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Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells
Human milk oligosaccharides (HMOS) are a complex mixture of bioactive components supporting the immune development of breastfed‐infants. Dendritic cells (DCs) play a central role in the regulation of immune responses, being specialized in antigen presentation and driving T‐cell priming as well as di...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619030/ https://www.ncbi.nlm.nih.gov/pubmed/30900752 http://dx.doi.org/10.1002/eji.201847971 |
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author | Xiao, Ling van De Worp, Wouter RPH Stassen, Roderick van Maastrigt, Celine Kettelarij, Nienke Stahl, Bernd Blijenberg, Bernadet Overbeek, Saskia A. Folkerts, Gert Garssen, Johan van't Land, Belinda |
author_facet | Xiao, Ling van De Worp, Wouter RPH Stassen, Roderick van Maastrigt, Celine Kettelarij, Nienke Stahl, Bernd Blijenberg, Bernadet Overbeek, Saskia A. Folkerts, Gert Garssen, Johan van't Land, Belinda |
author_sort | Xiao, Ling |
collection | PubMed |
description | Human milk oligosaccharides (HMOS) are a complex mixture of bioactive components supporting the immune development of breastfed‐infants. Dendritic cells (DCs) play a central role in the regulation of immune responses, being specialized in antigen presentation and driving T‐cell priming as well as differentiation. However, little is known about the direct effects of HMOS on human DC phenotypes and functions. Here, we report that HMOS mixture isolated from pooled human milk, induced semi‐maturation of human monocytes‐derived DCs (moDCs), and elevated levels of IL‐10, IL‐27 and IL‐6 but not IL‐12p70 and TNF‐α. Consistently, HMOS‐conditioned human moDCs promoted Treg generation from naïve CD4(+) T cells. Interestingly, HMOS limited LPS‐induced maturation of human moDCs, while maintained IL‐10 and IL‐27 secretion and reduced LPS‐induced production of IL‐12p70, IL‐6 and TNF‐α. Furthermore, HMOS+LPS‐stimulated DCs induced a higher frequency of Tregs and increased IL‐10 production, while a reduction in Tbet+Th1 frequency and IFN‐γ production was detected as compared to LPS‐DCs. The regulatory effects of HMOS seemed to be mediated by interactions of HMOS with receptors, including but not limited to TLR4 and DC‐SIGN on human moDCs. In conclusion, HMOS contain tolerogenic factors influencing human moDCs and thereby modulating the development of the neonatal immune system. |
format | Online Article Text |
id | pubmed-6619030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66190302019-07-22 Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells Xiao, Ling van De Worp, Wouter RPH Stassen, Roderick van Maastrigt, Celine Kettelarij, Nienke Stahl, Bernd Blijenberg, Bernadet Overbeek, Saskia A. Folkerts, Gert Garssen, Johan van't Land, Belinda Eur J Immunol Innate immunity Human milk oligosaccharides (HMOS) are a complex mixture of bioactive components supporting the immune development of breastfed‐infants. Dendritic cells (DCs) play a central role in the regulation of immune responses, being specialized in antigen presentation and driving T‐cell priming as well as differentiation. However, little is known about the direct effects of HMOS on human DC phenotypes and functions. Here, we report that HMOS mixture isolated from pooled human milk, induced semi‐maturation of human monocytes‐derived DCs (moDCs), and elevated levels of IL‐10, IL‐27 and IL‐6 but not IL‐12p70 and TNF‐α. Consistently, HMOS‐conditioned human moDCs promoted Treg generation from naïve CD4(+) T cells. Interestingly, HMOS limited LPS‐induced maturation of human moDCs, while maintained IL‐10 and IL‐27 secretion and reduced LPS‐induced production of IL‐12p70, IL‐6 and TNF‐α. Furthermore, HMOS+LPS‐stimulated DCs induced a higher frequency of Tregs and increased IL‐10 production, while a reduction in Tbet+Th1 frequency and IFN‐γ production was detected as compared to LPS‐DCs. The regulatory effects of HMOS seemed to be mediated by interactions of HMOS with receptors, including but not limited to TLR4 and DC‐SIGN on human moDCs. In conclusion, HMOS contain tolerogenic factors influencing human moDCs and thereby modulating the development of the neonatal immune system. John Wiley and Sons Inc. 2019-04-04 2019-07 /pmc/articles/PMC6619030/ /pubmed/30900752 http://dx.doi.org/10.1002/eji.201847971 Text en © 2019 The Authors. European Journal of Immunology published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Innate immunity Xiao, Ling van De Worp, Wouter RPH Stassen, Roderick van Maastrigt, Celine Kettelarij, Nienke Stahl, Bernd Blijenberg, Bernadet Overbeek, Saskia A. Folkerts, Gert Garssen, Johan van't Land, Belinda Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
title | Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
title_full | Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
title_fullStr | Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
title_full_unstemmed | Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
title_short | Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
title_sort | human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
topic | Innate immunity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619030/ https://www.ncbi.nlm.nih.gov/pubmed/30900752 http://dx.doi.org/10.1002/eji.201847971 |
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