Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells
The gut–liver axis is increasingly considered to play a vital part in the progression of chronic inflammatory gut and liver diseases. Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-dept...
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Veröffentlicht in: | Hepatology international 2018-07, Vol.12 (4), p.305-314 |
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description | The gut–liver axis is increasingly considered to play a vital part in the progression of chronic inflammatory gut and liver diseases. Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-depth the roles of regulatory T cells (Tregs) and mucosal-associated invariant T cells (MAITs) within the context of inflammatory bowel disease, primary sclerosing cholangitis, and non-alcoholic steatohepatitis. Tregs are crucial in maintaining peripheral tolerance and preventing autoimmunity. MAIT cells have a unique ability to rapidly recognize microbial metabolites and mount a local immune response and act as a ‘biliary firewall’ at the gut and biliary epithelial barrier. We also outline how current knowledge can be exploited to develop novel therapies to control the propagation of chronic gut- and liver-related inflammatory and autoimmune conditions. We specifically focus on the nature of the Tregs’ cell therapy product and outline an adjunctive role for low-dose IL-2. All in all, it is clear that translational immunology is at crucial crossroads. The success of ongoing clinical trials in cellular therapies for inflammatory gut and liver conditions could revolutionize the treatment of these conditions and the lives of our patients in the coming years. |
doi_str_mv | 10.1007/s12072-018-9882-x |
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Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-depth the roles of regulatory T cells (Tregs) and mucosal-associated invariant T cells (MAITs) within the context of inflammatory bowel disease, primary sclerosing cholangitis, and non-alcoholic steatohepatitis. Tregs are crucial in maintaining peripheral tolerance and preventing autoimmunity. MAIT cells have a unique ability to rapidly recognize microbial metabolites and mount a local immune response and act as a ‘biliary firewall’ at the gut and biliary epithelial barrier. We also outline how current knowledge can be exploited to develop novel therapies to control the propagation of chronic gut- and liver-related inflammatory and autoimmune conditions. We specifically focus on the nature of the Tregs’ cell therapy product and outline an adjunctive role for low-dose IL-2. All in all, it is clear that translational immunology is at crucial crossroads. The success of ongoing clinical trials in cellular therapies for inflammatory gut and liver conditions could revolutionize the treatment of these conditions and the lives of our patients in the coming years.</description><identifier>ISSN: 1936-0533</identifier><identifier>EISSN: 1936-0541</identifier><identifier>DOI: 10.1007/s12072-018-9882-x</identifier><identifier>PMID: 30027532</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Autoimmunity ; Cell therapy ; Cholangitis ; Cholangitis, Sclerosing - immunology ; Clinical trials ; Colorectal Surgery ; Crosstalk ; Hepatocytes ; Hepatology ; Humans ; Immune response ; Immune system ; Immunological tolerance ; Immunology ; Immunoregulation ; Inflammatory bowel diseases ; Inflammatory Bowel Diseases - immunology ; Interleukin 2 ; Intestine ; Invariants ; Liver ; Liver diseases ; Lymphocytes ; Lymphocytes T ; Medical research ; Medicine & Public Health ; Metabolites ; Microorganisms ; Mucosa ; Mucosal-Associated Invariant T Cells ; Non-alcoholic Fatty Liver Disease - immunology ; Regulatory mechanisms (biology) ; Review ; Review Article ; Surgery ; T-Lymphocytes, Regulatory</subject><ispartof>Hepatology international, 2018-07, Vol.12 (4), p.305-314</ispartof><rights>The Author(s) 2018. corrected publication 2022</rights><rights>Hepatology International is a copyright of Springer, (2018). 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Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-depth the roles of regulatory T cells (Tregs) and mucosal-associated invariant T cells (MAITs) within the context of inflammatory bowel disease, primary sclerosing cholangitis, and non-alcoholic steatohepatitis. Tregs are crucial in maintaining peripheral tolerance and preventing autoimmunity. MAIT cells have a unique ability to rapidly recognize microbial metabolites and mount a local immune response and act as a ‘biliary firewall’ at the gut and biliary epithelial barrier. We also outline how current knowledge can be exploited to develop novel therapies to control the propagation of chronic gut- and liver-related inflammatory and autoimmune conditions. We specifically focus on the nature of the Tregs’ cell therapy product and outline an adjunctive role for low-dose IL-2. All in all, it is clear that translational immunology is at crucial crossroads. The success of ongoing clinical trials in cellular therapies for inflammatory gut and liver conditions could revolutionize the treatment of these conditions and the lives of our patients in the coming years.</description><subject>Autoimmunity</subject><subject>Cell therapy</subject><subject>Cholangitis</subject><subject>Cholangitis, Sclerosing - immunology</subject><subject>Clinical trials</subject><subject>Colorectal Surgery</subject><subject>Crosstalk</subject><subject>Hepatocytes</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunological tolerance</subject><subject>Immunology</subject><subject>Immunoregulation</subject><subject>Inflammatory bowel diseases</subject><subject>Inflammatory Bowel Diseases - immunology</subject><subject>Interleukin 2</subject><subject>Intestine</subject><subject>Invariants</subject><subject>Liver</subject><subject>Liver diseases</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Medical research</subject><subject>Medicine & Public Health</subject><subject>Metabolites</subject><subject>Microorganisms</subject><subject>Mucosa</subject><subject>Mucosal-Associated Invariant T Cells</subject><subject>Non-alcoholic Fatty Liver Disease - immunology</subject><subject>Regulatory mechanisms (biology)</subject><subject>Review</subject><subject>Review Article</subject><subject>Surgery</subject><subject>T-Lymphocytes, Regulatory</subject><issn>1936-0533</issn><issn>1936-0541</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kUtv1DAUhS0EomXgB7BBltiwSfEjsWMWSKgCijQSm7K2rpM7qduMXWxnaP89SacdHhKsbOl-99jnHEJecnbCGdNvMxdMi4rxtjJtK6qbR-SYG6kq1tT88eEu5RF5lvMlY02juHpKjiRjQjdSHJNh7cOVDwMtF0iHqVAIPR39DtM72qWYc4HxijosPxADTThMI5SYbuk57XAc8x2_nbqYoYKcY-ehYE992EHyEMoD95w82cCY8cX9uSLfPn08Pz2r1l8_fzn9sK66plal4s5p3Ss0pjV9bRg0poO6VhuHgLUCJzmTzqDeNNo5wRF6BAFdy3vVGu7kirzf615Pbot9h6EkGO118ltItzaCt39Ogr-wQ9xZxYxmc2Ar8uZeIMXvE-Zitz4vFiBgnLKdE5dSclkv6Ou_0Ms4pTDbs0IzY2ppZPtfimlulGzNosX31F3oCTeHL3Nml7Ltvmw7l22Xsu3NvPPqd6-HjYd2Z0DsgTyPwoDp19P_Vv0JHim25A</recordid><startdate>20180701</startdate><enddate>20180701</enddate><creator>Atif, Muhammad</creator><creator>Warner, Suz</creator><creator>Oo, Ye H.</creator><general>Springer India</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180701</creationdate><title>Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells</title><author>Atif, Muhammad ; Warner, Suz ; Oo, Ye H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-1bb77d6e9989d490a59ca446fbeae46ab3103b9e7f57bb21eadea2ac81d6891b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Autoimmunity</topic><topic>Cell therapy</topic><topic>Cholangitis</topic><topic>Cholangitis, Sclerosing - immunology</topic><topic>Clinical trials</topic><topic>Colorectal Surgery</topic><topic>Crosstalk</topic><topic>Hepatocytes</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunological tolerance</topic><topic>Immunology</topic><topic>Immunoregulation</topic><topic>Inflammatory bowel diseases</topic><topic>Inflammatory Bowel Diseases - immunology</topic><topic>Interleukin 2</topic><topic>Intestine</topic><topic>Invariants</topic><topic>Liver</topic><topic>Liver diseases</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Medical research</topic><topic>Medicine & Public Health</topic><topic>Metabolites</topic><topic>Microorganisms</topic><topic>Mucosa</topic><topic>Mucosal-Associated Invariant T Cells</topic><topic>Non-alcoholic Fatty Liver Disease - immunology</topic><topic>Regulatory mechanisms (biology)</topic><topic>Review</topic><topic>Review Article</topic><topic>Surgery</topic><topic>T-Lymphocytes, Regulatory</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Atif, Muhammad</creatorcontrib><creatorcontrib>Warner, Suz</creatorcontrib><creatorcontrib>Oo, Ye H.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</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>Hepatology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Atif, Muhammad</au><au>Warner, Suz</au><au>Oo, Ye H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells</atitle><jtitle>Hepatology international</jtitle><stitle>Hepatol Int</stitle><addtitle>Hepatol Int</addtitle><date>2018-07-01</date><risdate>2018</risdate><volume>12</volume><issue>4</issue><spage>305</spage><epage>314</epage><pages>305-314</pages><issn>1936-0533</issn><eissn>1936-0541</eissn><abstract>The gut–liver axis is increasingly considered to play a vital part in the progression of chronic inflammatory gut and liver diseases. Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-depth the roles of regulatory T cells (Tregs) and mucosal-associated invariant T cells (MAITs) within the context of inflammatory bowel disease, primary sclerosing cholangitis, and non-alcoholic steatohepatitis. Tregs are crucial in maintaining peripheral tolerance and preventing autoimmunity. MAIT cells have a unique ability to rapidly recognize microbial metabolites and mount a local immune response and act as a ‘biliary firewall’ at the gut and biliary epithelial barrier. We also outline how current knowledge can be exploited to develop novel therapies to control the propagation of chronic gut- and liver-related inflammatory and autoimmune conditions. We specifically focus on the nature of the Tregs’ cell therapy product and outline an adjunctive role for low-dose IL-2. All in all, it is clear that translational immunology is at crucial crossroads. The success of ongoing clinical trials in cellular therapies for inflammatory gut and liver conditions could revolutionize the treatment of these conditions and the lives of our patients in the coming years.</abstract><cop>New Delhi</cop><pub>Springer India</pub><pmid>30027532</pmid><doi>10.1007/s12072-018-9882-x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Autoimmunity Cell therapy Cholangitis Cholangitis, Sclerosing - immunology Clinical trials Colorectal Surgery Crosstalk Hepatocytes Hepatology Humans Immune response Immune system Immunological tolerance Immunology Immunoregulation Inflammatory bowel diseases Inflammatory Bowel Diseases - immunology Interleukin 2 Intestine Invariants Liver Liver diseases Lymphocytes Lymphocytes T Medical research Medicine & Public Health Metabolites Microorganisms Mucosa Mucosal-Associated Invariant T Cells Non-alcoholic Fatty Liver Disease - immunology Regulatory mechanisms (biology) Review Review Article Surgery T-Lymphocytes, Regulatory |
title | Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells |
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