The Impact of Short-Chain Fatty Acids on Neonatal Regulatory T Cells
Over the first weeks of life, the neonatal gastrointestinal tract is rapidly colonised by a diverse range of microbial species that come to form the ‘gut microbiota’. Microbial colonisation of the neonatal gut is a well-established regulator of several physiological processes that contribute to immu...
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description | Over the first weeks of life, the neonatal gastrointestinal tract is rapidly colonised by a diverse range of microbial species that come to form the ‘gut microbiota’. Microbial colonisation of the neonatal gut is a well-established regulator of several physiological processes that contribute to immunological protection in postnatal life, including the development of the intestinal mucosa and adaptive immunity. However, the specific microbiota-derived signals that mediate these processes have not yet been fully characterised. Accumulating evidence suggests short-chain fatty acids (SCFAs), end-products of intestinal bacterial metabolism, as one of the key mediators of immune development in early life. Critical to neonatal health is the development of regulatory T (Treg) cells that promote and maintain immunological tolerance against self and innocuous antigens. Several studies have shown that SCFAs can induce the differentiation and expansion of Tregs but also mediate pathological effects in abnormal amounts. However, the exact mechanisms through which SCFAs regulate Treg development and pathologies in early life remain poorly defined. In this review, we summarise the current knowledge surrounding SCFAs and their potential impact on the neonatal immune system with a particular focus on Tregs, and the possible mechanisms through which SCFAs achieve their immune modulatory effect. |
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Microbial colonisation of the neonatal gut is a well-established regulator of several physiological processes that contribute to immunological protection in postnatal life, including the development of the intestinal mucosa and adaptive immunity. However, the specific microbiota-derived signals that mediate these processes have not yet been fully characterised. Accumulating evidence suggests short-chain fatty acids (SCFAs), end-products of intestinal bacterial metabolism, as one of the key mediators of immune development in early life. Critical to neonatal health is the development of regulatory T (Treg) cells that promote and maintain immunological tolerance against self and innocuous antigens. Several studies have shown that SCFAs can induce the differentiation and expansion of Tregs but also mediate pathological effects in abnormal amounts. However, the exact mechanisms through which SCFAs regulate Treg development and pathologies in early life remain poorly defined. In this review, we summarise the current knowledge surrounding SCFAs and their potential impact on the neonatal immune system with a particular focus on Tregs, and the possible mechanisms through which SCFAs achieve their immune modulatory effect.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu14183670</identifier><identifier>PMID: 36145046</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Adaptive immunity ; Antigens ; Autoantigens ; B cells ; Colonization ; Cytokines ; Cytotoxicity ; Digestive system ; Fatty acids ; Gastrointestinal system ; Gastrointestinal tract ; Health aspects ; Immune system ; Immunological tolerance ; Immunology ; Immunoregulation ; Infants (Newborn) ; Inflammation ; Intestinal microflora ; Intestine ; Lymphocytes ; Lymphocytes T ; Metabolism ; Microbiota ; Microbiota (Symbiotic organisms) ; Microorganisms ; Mucosal immunity ; Neonates ; Pathogens ; Pathological effects ; Pediatric research ; Physiological aspects ; Review ; Signal processing ; Suppressor cells ; T cell receptors ; T cells ; Thymus gland</subject><ispartof>Nutrients, 2022-09, Vol.14 (18), p.3670</ispartof><rights>COPYRIGHT 2022 MDPI AG</rights><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Microbial colonisation of the neonatal gut is a well-established regulator of several physiological processes that contribute to immunological protection in postnatal life, including the development of the intestinal mucosa and adaptive immunity. However, the specific microbiota-derived signals that mediate these processes have not yet been fully characterised. Accumulating evidence suggests short-chain fatty acids (SCFAs), end-products of intestinal bacterial metabolism, as one of the key mediators of immune development in early life. Critical to neonatal health is the development of regulatory T (Treg) cells that promote and maintain immunological tolerance against self and innocuous antigens. Several studies have shown that SCFAs can induce the differentiation and expansion of Tregs but also mediate pathological effects in abnormal amounts. However, the exact mechanisms through which SCFAs regulate Treg development and pathologies in early life remain poorly defined. 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Toldi, Gergely</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-ed5c806ae66f2d1497673cb1d73c7374be0c70c3f330b92cfea80631e074e1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adaptive immunity</topic><topic>Antigens</topic><topic>Autoantigens</topic><topic>B cells</topic><topic>Colonization</topic><topic>Cytokines</topic><topic>Cytotoxicity</topic><topic>Digestive system</topic><topic>Fatty acids</topic><topic>Gastrointestinal system</topic><topic>Gastrointestinal tract</topic><topic>Health aspects</topic><topic>Immune system</topic><topic>Immunological tolerance</topic><topic>Immunology</topic><topic>Immunoregulation</topic><topic>Infants (Newborn)</topic><topic>Inflammation</topic><topic>Intestinal microflora</topic><topic>Intestine</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Metabolism</topic><topic>Microbiota</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>Microorganisms</topic><topic>Mucosal immunity</topic><topic>Neonates</topic><topic>Pathogens</topic><topic>Pathological effects</topic><topic>Pediatric research</topic><topic>Physiological aspects</topic><topic>Review</topic><topic>Signal processing</topic><topic>Suppressor cells</topic><topic>T cell receptors</topic><topic>T cells</topic><topic>Thymus gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chun, Jessica</creatorcontrib><creatorcontrib>Toldi, Gergely</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nutrients</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chun, Jessica</au><au>Toldi, Gergely</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Impact of Short-Chain Fatty Acids on Neonatal Regulatory T Cells</atitle><jtitle>Nutrients</jtitle><date>2022-09-06</date><risdate>2022</risdate><volume>14</volume><issue>18</issue><spage>3670</spage><pages>3670-</pages><issn>2072-6643</issn><eissn>2072-6643</eissn><abstract>Over the first weeks of life, the neonatal gastrointestinal tract is rapidly colonised by a diverse range of microbial species that come to form the ‘gut microbiota’. Microbial colonisation of the neonatal gut is a well-established regulator of several physiological processes that contribute to immunological protection in postnatal life, including the development of the intestinal mucosa and adaptive immunity. However, the specific microbiota-derived signals that mediate these processes have not yet been fully characterised. Accumulating evidence suggests short-chain fatty acids (SCFAs), end-products of intestinal bacterial metabolism, as one of the key mediators of immune development in early life. Critical to neonatal health is the development of regulatory T (Treg) cells that promote and maintain immunological tolerance against self and innocuous antigens. Several studies have shown that SCFAs can induce the differentiation and expansion of Tregs but also mediate pathological effects in abnormal amounts. However, the exact mechanisms through which SCFAs regulate Treg development and pathologies in early life remain poorly defined. 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subjects | Adaptive immunity Antigens Autoantigens B cells Colonization Cytokines Cytotoxicity Digestive system Fatty acids Gastrointestinal system Gastrointestinal tract Health aspects Immune system Immunological tolerance Immunology Immunoregulation Infants (Newborn) Inflammation Intestinal microflora Intestine Lymphocytes Lymphocytes T Metabolism Microbiota Microbiota (Symbiotic organisms) Microorganisms Mucosal immunity Neonates Pathogens Pathological effects Pediatric research Physiological aspects Review Signal processing Suppressor cells T cell receptors T cells Thymus gland |
title | The Impact of Short-Chain Fatty Acids on Neonatal Regulatory T Cells |
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