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Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery

Obesity and type 2 diabetes (T2D) are growing burdens for individuals and the health-care system. Bariatric surgery is an efficient, but drastic treatment to reduce body weight, normalize glucose values, and reduce low-grade inflammation. The gut microbiome, which is in part controlled by intestinal...

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Autores principales: Scheithauer, Torsten P.M., Davids, Mark, Winkelmeijer, Maaike, Verdoes, Xanthe, Aydin, Ömrüm, de Brauw, Maurits, van de Laar, Arnold, Meijnikman, Abraham S., Gerdes, Victor E.A., van Raalte, Daniël, Herrema, Hilde, Nieuwdorp, Max
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824225/
https://www.ncbi.nlm.nih.gov/pubmed/35130127
http://dx.doi.org/10.1080/19490976.2022.2031696
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author Scheithauer, Torsten P.M.
Davids, Mark
Winkelmeijer, Maaike
Verdoes, Xanthe
Aydin, Ömrüm
de Brauw, Maurits
van de Laar, Arnold
Meijnikman, Abraham S.
Gerdes, Victor E.A.
van Raalte, Daniël
Herrema, Hilde
Nieuwdorp, Max
author_facet Scheithauer, Torsten P.M.
Davids, Mark
Winkelmeijer, Maaike
Verdoes, Xanthe
Aydin, Ömrüm
de Brauw, Maurits
van de Laar, Arnold
Meijnikman, Abraham S.
Gerdes, Victor E.A.
van Raalte, Daniël
Herrema, Hilde
Nieuwdorp, Max
author_sort Scheithauer, Torsten P.M.
collection PubMed
description Obesity and type 2 diabetes (T2D) are growing burdens for individuals and the health-care system. Bariatric surgery is an efficient, but drastic treatment to reduce body weight, normalize glucose values, and reduce low-grade inflammation. The gut microbiome, which is in part controlled by intestinal antibodies, such as IgA, is involved in the development of both conditions. Knowledge of the effect of bariatric surgery on systemic and intestinal antibody response is limited. Here, we determined the fecal antibody and gut microbiome response in 40 T2D and non-diabetic (ND) obese individuals that underwent bariatric surgery (N = 40). Body weight, fasting glucose concentrations and inflammatory parameters decreased after bariatric surgery, whereas pro-inflammatory bacterial species such as lipopolysaccharide (LPS), and flagellin increased in the feces. Simultaneously, concentrations of LPS- and flagellin-specific intestinal IgA levels increased with the majority of pro-inflammatory bacteria coated with IgA after surgery. Finally, serum antibodies decreased in both groups, along with a lower inflammatory tone. We conclude that intestinal rearrangement by bariatric surgery leads to expansion of typical pro-inflammatory bacteria, which may be compensated by an improved antibody response. Although further evidence and mechanistic insights are needed, we postulate that this apparent compensatory antibody response might help to reduce systemic inflammation by neutralizing intestinal immunogenic components and thereby enhance intestinal barrier function after bariatric surgery.
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spelling pubmed-88242252022-02-09 Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery Scheithauer, Torsten P.M. Davids, Mark Winkelmeijer, Maaike Verdoes, Xanthe Aydin, Ömrüm de Brauw, Maurits van de Laar, Arnold Meijnikman, Abraham S. Gerdes, Victor E.A. van Raalte, Daniël Herrema, Hilde Nieuwdorp, Max Gut Microbes Research Paper Obesity and type 2 diabetes (T2D) are growing burdens for individuals and the health-care system. Bariatric surgery is an efficient, but drastic treatment to reduce body weight, normalize glucose values, and reduce low-grade inflammation. The gut microbiome, which is in part controlled by intestinal antibodies, such as IgA, is involved in the development of both conditions. Knowledge of the effect of bariatric surgery on systemic and intestinal antibody response is limited. Here, we determined the fecal antibody and gut microbiome response in 40 T2D and non-diabetic (ND) obese individuals that underwent bariatric surgery (N = 40). Body weight, fasting glucose concentrations and inflammatory parameters decreased after bariatric surgery, whereas pro-inflammatory bacterial species such as lipopolysaccharide (LPS), and flagellin increased in the feces. Simultaneously, concentrations of LPS- and flagellin-specific intestinal IgA levels increased with the majority of pro-inflammatory bacteria coated with IgA after surgery. Finally, serum antibodies decreased in both groups, along with a lower inflammatory tone. We conclude that intestinal rearrangement by bariatric surgery leads to expansion of typical pro-inflammatory bacteria, which may be compensated by an improved antibody response. Although further evidence and mechanistic insights are needed, we postulate that this apparent compensatory antibody response might help to reduce systemic inflammation by neutralizing intestinal immunogenic components and thereby enhance intestinal barrier function after bariatric surgery. Taylor & Francis 2022-02-07 /pmc/articles/PMC8824225/ /pubmed/35130127 http://dx.doi.org/10.1080/19490976.2022.2031696 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Scheithauer, Torsten P.M.
Davids, Mark
Winkelmeijer, Maaike
Verdoes, Xanthe
Aydin, Ömrüm
de Brauw, Maurits
van de Laar, Arnold
Meijnikman, Abraham S.
Gerdes, Victor E.A.
van Raalte, Daniël
Herrema, Hilde
Nieuwdorp, Max
Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery
title Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery
title_full Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery
title_fullStr Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery
title_full_unstemmed Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery
title_short Compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery
title_sort compensatory intestinal antibody response against pro-inflammatory microbiota after bariatric surgery
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824225/
https://www.ncbi.nlm.nih.gov/pubmed/35130127
http://dx.doi.org/10.1080/19490976.2022.2031696
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