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      Butyrate as a bioactive human milk protective component against food allergy

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          Abstract

          Background

          Food allergy (FA) is a growing health problem worldwide. Effective strategies are advocated to limit the disease burden. Human milk (HM) could be considered as a protective factor against FA, but its mechanisms remain unclear. Butyrate is a gut microbiota‐derived metabolite able to exert several immunomodulatory functions. We aimed to define the butyrate concentration in HM, and to see whether the butyrate concentration detected in HM is able to modulate the mechanisms of immune tolerance.

          Methods

          HM butyrate concentration from 109 healthy women was assessed by GS‐MS. The effect of HM butyrate on tolerogenic mechanisms was assessed in in vivo and in vitro models.

          Results

          The median butyrate concentration in mature HM was 0.75 mM. This butyrate concentration was responsible for the maximum modulatory effects observed in all experimental models evaluated in this study. Data from mouse model show that in basal condition, butyrate up‐regulated the expression of several biomarkers of gut barrier integrity, and of tolerogenic cytokines. Pretreatment with butyrate significantly reduced allergic response in three animal models of FA, with a stimulation of tolerogenic cytokines, inhibition of Th2 cytokines production and a modulation of oxidative stress. Data from human cell models show that butyrate stimulated human beta defensin‐3, mucus components and tight junctions expression in human enterocytes, and IL‐10, IFN‐γ and FoxP3 expression through epigenetic mechanisms in PBMCs from FA children. Furthermore, it promoted the precursors of M2 macrophages, DCs and regulatory T cells.

          Conclusion

          The study's findings suggest the importance of butyrate as a pivotal HM compound able to protect against FA.

          Abstract

          Human milk contains a significant level of the short‐chain fatty acid butyrate. At concentration detectable in human milk, butyrate effectively modulates several tolerogenic mechanisms involved in the protection against food allergy. The protective role of human milk against food allergy could be related, at least in part, to the presence of an effective concentration of butyrate

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          Most cited references85

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          From Dietary Fiber to Host Physiology: Short-Chain Fatty Acids as Key Bacterial Metabolites.

          A compelling set of links between the composition of the gut microbiota, the host diet, and host physiology has emerged. Do these links reflect cause-and-effect relationships, and what might be their mechanistic basis? A growing body of work implicates microbially produced metabolites as crucial executors of diet-based microbial influence on the host. Here, we will review data supporting the diverse functional roles carried out by a major class of bacterial metabolites, the short-chain fatty acids (SCFAs). SCFAs can directly activate G-coupled-receptors, inhibit histone deacetylases, and serve as energy substrates. They thus affect various physiological processes and may contribute to health and disease.
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            The microbial metabolites, short-chain fatty acids, regulate colonic Treg cell homeostasis.

            Regulatory T cells (Tregs) that express the transcription factor Foxp3 are critical for regulating intestinal inflammation. Candidate microbe approaches have identified bacterial species and strain-specific molecules that can affect intestinal immune responses, including species that modulate Treg responses. Because neither all humans nor mice harbor the same bacterial strains, we posited that more prevalent factors exist that regulate the number and function of colonic Tregs. We determined that short-chain fatty acids, gut microbiota-derived bacterial fermentation products, regulate the size and function of the colonic Treg pool and protect against colitis in a Ffar2-dependent manner in mice. Our study reveals that a class of abundant microbial metabolites underlies adaptive immune microbiota coadaptation and promotes colonic homeostasis and health.
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              Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells.

              Gut commensal microbes shape the mucosal immune system by regulating the differentiation and expansion of several types of T cell. Clostridia, a dominant class of commensal microbe, can induce colonic regulatory T (Treg) cells, which have a central role in the suppression of inflammatory and allergic responses. However, the molecular mechanisms by which commensal microbes induce colonic Treg cells have been unclear. Here we show that a large bowel microbial fermentation product, butyrate, induces the differentiation of colonic Treg cells in mice. A comparative NMR-based metabolome analysis suggests that the luminal concentrations of short-chain fatty acids positively correlates with the number of Treg cells in the colon. Among short-chain fatty acids, butyrate induced the differentiation of Treg cells in vitro and in vivo, and ameliorated the development of colitis induced by adoptive transfer of CD4(+) CD45RB(hi) T cells in Rag1(-/-) mice. Treatment of naive T cells under the Treg-cell-polarizing conditions with butyrate enhanced histone H3 acetylation in the promoter and conserved non-coding sequence regions of the Foxp3 locus, suggesting a possible mechanism for how microbial-derived butyrate regulates the differentiation of Treg cells. Our findings provide new insight into the mechanisms by which host-microbe interactions establish immunological homeostasis in the gut.
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                Author and article information

                Contributors
                berni@unina.it
                Journal
                Allergy
                Allergy
                10.1111/(ISSN)1398-9995
                ALL
                Allergy
                John Wiley and Sons Inc. (Hoboken )
                0105-4538
                1398-9995
                16 November 2020
                May 2021
                : 76
                : 5 ( doiID: 10.1111/all.v76.5 )
                : 1398-1415
                Affiliations
                [ 1 ] Department of Translational Medical Science University of Naples Federico II Naples Italy
                [ 2 ] ImmunoNutritionLab at the CEINGE‐Biotecnologie Avanzate s.c.ar.l Research Center University of Naples Federico II Naples Italy
                [ 3 ] European Laboratory for the Investigation of Food‐Induced Diseases University of Naples Federico II Naples Italy
                [ 4 ] Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana" University of Salerno Fisciano Italy
                [ 5 ] Department of Pharmacy University of Naples Federico II Naples Italy
                [ 6 ] Department of Biology University of Naples Federico II Naples Italy
                [ 7 ] Department of Pediatric Cardiology Monaldi Hospital Naples Italy
                [ 8 ] Neonatal Intensive Care Unit "Betania" Evangelical Hospital Naples Italy
                [ 9 ] Cardiovascular Research Unit IRCCS MultiMedica Milan Italy
                [ 10 ] Task Force for Microbiome Studies University of Naples Federico II Naples Italy
                Author notes
                [*] [* ] Correspondence

                Roberto Berni Canani, Chief of the Pediatric Allergy Program at the Department of Translational Medical Science; Chief of the ImmunoNutritionLab at CEINGE – Advanced Biotechnologies, University of Naples “Federico II” Via S. Pansini 5 80131 Naples, Italy.

                Email: berni@ 123456unina.it

                Author information
                https://orcid.org/0000-0002-5562-1408
                https://orcid.org/0000-0003-4681-546X
                https://orcid.org/0000-0002-8518-2047
                https://orcid.org/0000-0002-5169-9574
                Article
                ALL14625
                10.1111/all.14625
                8247419
                33043467
                1e570d64-b540-402c-81ad-d443535ae526
                © 2020 The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 31 August 2020
                : 22 April 2020
                : 10 September 2020
                Page count
                Figures: 8, Tables: 0, Pages: 18, Words: 11896
                Funding
                Funded by: Italian Ministry of Health
                Award ID: PE‐2011‐02348447
                Award ID: RF‐2011‐02348194
                Funded by: Cariplo Foundation , open-funder-registry 10.13039/501100002803;
                Award ID: 2016‐0874
                Funded by: Italian Ministry of the University and Scientific Research
                Award ID: PRIN‐20157ATSLF_009
                Funded by: Umberto Veronesi Foundation
                Award ID: FUV 2017 cod.1072
                Award ID: FUV 2018 cod.2153
                Award ID: FUV 2019 cod.2798
                Categories
                Original Article
                ORIGINAL ARTICLES
                Basic and Translational Allergy Immunology
                Custom metadata
                2.0
                May 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.2 mode:remove_FC converted:01.07.2021

                Immunology
                breast milk,immune tolerance,short‐chain fatty acids,tolerogenic mechanism
                Immunology
                breast milk, immune tolerance, short‐chain fatty acids, tolerogenic mechanism

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