Human retinoic acid–regulated CD161+ regulatory T cells support wound repair in intestinal mucosa
Repair of tissue damaged during inflammatory processes is key to the return of local homeostasis and restoration of epithelial integrity. Here we describe CD161 + regulatory T (T reg ) cells as a distinct, highly suppressive population of T reg cells that mediate wound healing. These T reg cells wer...
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Veröffentlicht in: | Nature immunology 2018-12, Vol.19 (12), p.1403-1414 |
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creator | Povoleri, Giovanni A. M. Nova-Lamperti, Estefania Scottà, Cristiano Fanelli, Giorgia Chen, Yun-Ching Becker, Pablo D. Boardman, Dominic Costantini, Benedetta Romano, Marco Pavlidis, Polychronis McGregor, Reuben Pantazi, Eirini Chauss, Daniel Sun, Hong-Wei Shih, Han-Yu Cousins, David J. Cooper, Nichola Powell, Nick Kemper, Claudia Pirooznia, Mehdi Laurence, Arian Kordasti, Shahram Kazemian, Majid Lombardi, Giovanna Afzali, Behdad |
description | Repair of tissue damaged during inflammatory processes is key to the return of local homeostasis and restoration of epithelial integrity. Here we describe CD161
+
regulatory T (T
reg
) cells as a distinct, highly suppressive population of T
reg
cells that mediate wound healing. These T
reg
cells were enriched in intestinal lamina propria, particularly in Crohn’s disease. CD161
+
T
reg
cells had an all-
trans
retinoic acid (ATRA)-regulated gene signature, and CD161 expression on T
reg
cells was induced by ATRA, which directly regulated the
CD161
gene. CD161 was co-stimulatory, and ligation with the T cell antigen receptor induced cytokines that accelerated the wound healing of intestinal epithelial cells. We identified a transcription-factor network, including BACH2, RORγt, FOSL2, AP-1 and RUNX1, that controlled expression of the wound-healing program, and found a CD161
+
T
reg
cell signature in Crohn’s disease mucosa associated with reduced inflammation. These findings identify CD161
+
T
reg
cells as a population involved in controlling the balance between inflammation and epithelial barrier healing in the gut.
T
reg
cells are essential for enforcing peripheral tolerance but can also influence tissue regeneration. Afzali and colleagues use high-dimensional analysis to describe a distinct population of CD161
+
human T
reg
cells involved in wound healing of the intestinal mucosa. |
doi_str_mv | 10.1038/s41590-018-0230-z |
format | Article |
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+
regulatory T (T
reg
) cells as a distinct, highly suppressive population of T
reg
cells that mediate wound healing. These T
reg
cells were enriched in intestinal lamina propria, particularly in Crohn’s disease. CD161
+
T
reg
cells had an all-
trans
retinoic acid (ATRA)-regulated gene signature, and CD161 expression on T
reg
cells was induced by ATRA, which directly regulated the
CD161
gene. CD161 was co-stimulatory, and ligation with the T cell antigen receptor induced cytokines that accelerated the wound healing of intestinal epithelial cells. We identified a transcription-factor network, including BACH2, RORγt, FOSL2, AP-1 and RUNX1, that controlled expression of the wound-healing program, and found a CD161
+
T
reg
cell signature in Crohn’s disease mucosa associated with reduced inflammation. These findings identify CD161
+
T
reg
cells as a population involved in controlling the balance between inflammation and epithelial barrier healing in the gut.
T
reg
cells are essential for enforcing peripheral tolerance but can also influence tissue regeneration. Afzali and colleagues use high-dimensional analysis to describe a distinct population of CD161
+
human T
reg
cells involved in wound healing of the intestinal mucosa.</description><identifier>ISSN: 1529-2908</identifier><identifier>EISSN: 1529-2916</identifier><identifier>DOI: 10.1038/s41590-018-0230-z</identifier><identifier>PMID: 30397350</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/250/1619/554/1898/1271 ; 631/250/2152/569 ; Activator protein 1 ; Biomedical and Life Sciences ; Biomedicine ; Crohn Disease - immunology ; Crohn's disease ; Epithelial cells ; Homeostasis ; Humans ; Immunology ; Immunoregulation ; Infectious Diseases ; Inflammation ; Intestinal Mucosa - immunology ; Intestine ; Lamina propria ; Lymphocytes ; Lymphocytes T ; Mucosa ; NK Cell Lectin-Like Receptor Subfamily B - immunology ; Retinoic acid ; Runx1 protein ; T-Lymphocyte Subsets - immunology ; T-Lymphocytes, Regulatory - immunology ; Transcription factors ; Tretinoin - immunology ; Wound healing ; Wound Healing - immunology</subject><ispartof>Nature immunology, 2018-12, Vol.19 (12), p.1403-1414</ispartof><rights>The Author(s), under exclusive licence to Springer Nature America, Inc. 2018</rights><rights>Copyright Nature Publishing Group Dec 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-b5ee770627d6b1a17ba61bf4d8c28bfdb0bf6ed2444c8cb06ccb20b90852644a3</citedby><cites>FETCH-LOGICAL-c470t-b5ee770627d6b1a17ba61bf4d8c28bfdb0bf6ed2444c8cb06ccb20b90852644a3</cites><orcidid>0000-0003-2968-1156 ; 0000-0003-1980-1230 ; 0000-0003-3821-9596 ; 0000-0003-0342-651X ; 0000-0002-7525-5433</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30397350$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Povoleri, Giovanni A. M.</creatorcontrib><creatorcontrib>Nova-Lamperti, Estefania</creatorcontrib><creatorcontrib>Scottà, Cristiano</creatorcontrib><creatorcontrib>Fanelli, Giorgia</creatorcontrib><creatorcontrib>Chen, Yun-Ching</creatorcontrib><creatorcontrib>Becker, Pablo D.</creatorcontrib><creatorcontrib>Boardman, Dominic</creatorcontrib><creatorcontrib>Costantini, Benedetta</creatorcontrib><creatorcontrib>Romano, Marco</creatorcontrib><creatorcontrib>Pavlidis, Polychronis</creatorcontrib><creatorcontrib>McGregor, Reuben</creatorcontrib><creatorcontrib>Pantazi, Eirini</creatorcontrib><creatorcontrib>Chauss, Daniel</creatorcontrib><creatorcontrib>Sun, Hong-Wei</creatorcontrib><creatorcontrib>Shih, Han-Yu</creatorcontrib><creatorcontrib>Cousins, David J.</creatorcontrib><creatorcontrib>Cooper, Nichola</creatorcontrib><creatorcontrib>Powell, Nick</creatorcontrib><creatorcontrib>Kemper, Claudia</creatorcontrib><creatorcontrib>Pirooznia, Mehdi</creatorcontrib><creatorcontrib>Laurence, Arian</creatorcontrib><creatorcontrib>Kordasti, Shahram</creatorcontrib><creatorcontrib>Kazemian, Majid</creatorcontrib><creatorcontrib>Lombardi, Giovanna</creatorcontrib><creatorcontrib>Afzali, Behdad</creatorcontrib><title>Human retinoic acid–regulated CD161+ regulatory T cells support wound repair in intestinal mucosa</title><title>Nature immunology</title><addtitle>Nat Immunol</addtitle><addtitle>Nat Immunol</addtitle><description>Repair of tissue damaged during inflammatory processes is key to the return of local homeostasis and restoration of epithelial integrity. Here we describe CD161
+
regulatory T (T
reg
) cells as a distinct, highly suppressive population of T
reg
cells that mediate wound healing. These T
reg
cells were enriched in intestinal lamina propria, particularly in Crohn’s disease. CD161
+
T
reg
cells had an all-
trans
retinoic acid (ATRA)-regulated gene signature, and CD161 expression on T
reg
cells was induced by ATRA, which directly regulated the
CD161
gene. CD161 was co-stimulatory, and ligation with the T cell antigen receptor induced cytokines that accelerated the wound healing of intestinal epithelial cells. We identified a transcription-factor network, including BACH2, RORγt, FOSL2, AP-1 and RUNX1, that controlled expression of the wound-healing program, and found a CD161
+
T
reg
cell signature in Crohn’s disease mucosa associated with reduced inflammation. These findings identify CD161
+
T
reg
cells as a population involved in controlling the balance between inflammation and epithelial barrier healing in the gut.
T
reg
cells are essential for enforcing peripheral tolerance but can also influence tissue regeneration. Afzali and colleagues use high-dimensional analysis to describe a distinct population of CD161
+
human T
reg
cells involved in wound healing of the intestinal mucosa.</description><subject>631/250/1619/554/1898/1271</subject><subject>631/250/2152/569</subject><subject>Activator protein 1</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Crohn Disease - immunology</subject><subject>Crohn's disease</subject><subject>Epithelial cells</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Immunology</subject><subject>Immunoregulation</subject><subject>Infectious Diseases</subject><subject>Inflammation</subject><subject>Intestinal Mucosa - immunology</subject><subject>Intestine</subject><subject>Lamina propria</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Mucosa</subject><subject>NK Cell Lectin-Like Receptor Subfamily B - immunology</subject><subject>Retinoic acid</subject><subject>Runx1 protein</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>Transcription factors</subject><subject>Tretinoin - immunology</subject><subject>Wound healing</subject><subject>Wound Healing - immunology</subject><issn>1529-2908</issn><issn>1529-2916</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kd9KHDEUxkOp1D_tA_SmBHojlNGTTCYzcyPI2qogeGOvQ5LJbCMzkzGZKOuV7-Ab-iRmu-tWhUIgIed3vpMvH0JfCRwQyKvDwEhRQwakyoDmkN1_QDukoHVGa8I_bs5QbaPdEK4BCCs5-4S2c8jrMi9gB-mz2MsBezPZwVmNpbbN08OjN_PYyck0eHZCOPmB1xfOL_AV1qbrAg5xHJ2f8J2LQ5OAUVqP7ZDWZEKSkx3uo3ZBfkZbreyC-bLe99DvXz-vZmfZxeXp-ez4ItOshClThTFlCZyWDVdEklJJTlTLmkrTSrWNAtVy01DGmK60Aq61oqCSvYJyxmS-h45WumNUvWm0GSYvOzF620u_EE5a8bYy2D9i7m4FZyXjRZ0E9tcC3t3EZEL0NizNysG4GAQl6eOAc5In9Ps79NpFnzz_pRitoKI0UWRFae9C8KbdPIaAWEYoVhGKFKFYRijuU8-31y42HS-ZJYCugJBKw9z4f6P_r_oMUwCp3w</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Povoleri, Giovanni A. M.</creator><creator>Nova-Lamperti, Estefania</creator><creator>Scottà, Cristiano</creator><creator>Fanelli, Giorgia</creator><creator>Chen, Yun-Ching</creator><creator>Becker, Pablo D.</creator><creator>Boardman, Dominic</creator><creator>Costantini, Benedetta</creator><creator>Romano, Marco</creator><creator>Pavlidis, Polychronis</creator><creator>McGregor, Reuben</creator><creator>Pantazi, Eirini</creator><creator>Chauss, Daniel</creator><creator>Sun, Hong-Wei</creator><creator>Shih, Han-Yu</creator><creator>Cousins, David J.</creator><creator>Cooper, Nichola</creator><creator>Powell, Nick</creator><creator>Kemper, Claudia</creator><creator>Pirooznia, Mehdi</creator><creator>Laurence, Arian</creator><creator>Kordasti, Shahram</creator><creator>Kazemian, Majid</creator><creator>Lombardi, Giovanna</creator><creator>Afzali, Behdad</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</general><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>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2968-1156</orcidid><orcidid>https://orcid.org/0000-0003-1980-1230</orcidid><orcidid>https://orcid.org/0000-0003-3821-9596</orcidid><orcidid>https://orcid.org/0000-0003-0342-651X</orcidid><orcidid>https://orcid.org/0000-0002-7525-5433</orcidid></search><sort><creationdate>20181201</creationdate><title>Human retinoic acid–regulated CD161+ regulatory T cells support wound repair in intestinal mucosa</title><author>Povoleri, Giovanni A. M. ; Nova-Lamperti, Estefania ; Scottà, Cristiano ; Fanelli, Giorgia ; Chen, Yun-Ching ; Becker, Pablo D. ; Boardman, Dominic ; Costantini, Benedetta ; Romano, Marco ; Pavlidis, Polychronis ; McGregor, Reuben ; Pantazi, Eirini ; Chauss, Daniel ; Sun, Hong-Wei ; Shih, Han-Yu ; Cousins, David J. ; Cooper, Nichola ; Powell, Nick ; Kemper, Claudia ; Pirooznia, Mehdi ; Laurence, Arian ; Kordasti, Shahram ; Kazemian, Majid ; Lombardi, Giovanna ; Afzali, Behdad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-b5ee770627d6b1a17ba61bf4d8c28bfdb0bf6ed2444c8cb06ccb20b90852644a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>631/250/1619/554/1898/1271</topic><topic>631/250/2152/569</topic><topic>Activator protein 1</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Crohn Disease - immunology</topic><topic>Crohn's disease</topic><topic>Epithelial cells</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Immunology</topic><topic>Immunoregulation</topic><topic>Infectious Diseases</topic><topic>Inflammation</topic><topic>Intestinal Mucosa - immunology</topic><topic>Intestine</topic><topic>Lamina propria</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Mucosa</topic><topic>NK Cell Lectin-Like Receptor Subfamily B - immunology</topic><topic>Retinoic acid</topic><topic>Runx1 protein</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>Transcription factors</topic><topic>Tretinoin - immunology</topic><topic>Wound healing</topic><topic>Wound Healing - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Povoleri, Giovanni A. M.</creatorcontrib><creatorcontrib>Nova-Lamperti, Estefania</creatorcontrib><creatorcontrib>Scottà, Cristiano</creatorcontrib><creatorcontrib>Fanelli, Giorgia</creatorcontrib><creatorcontrib>Chen, Yun-Ching</creatorcontrib><creatorcontrib>Becker, Pablo D.</creatorcontrib><creatorcontrib>Boardman, Dominic</creatorcontrib><creatorcontrib>Costantini, Benedetta</creatorcontrib><creatorcontrib>Romano, Marco</creatorcontrib><creatorcontrib>Pavlidis, Polychronis</creatorcontrib><creatorcontrib>McGregor, Reuben</creatorcontrib><creatorcontrib>Pantazi, Eirini</creatorcontrib><creatorcontrib>Chauss, Daniel</creatorcontrib><creatorcontrib>Sun, Hong-Wei</creatorcontrib><creatorcontrib>Shih, Han-Yu</creatorcontrib><creatorcontrib>Cousins, David J.</creatorcontrib><creatorcontrib>Cooper, Nichola</creatorcontrib><creatorcontrib>Powell, Nick</creatorcontrib><creatorcontrib>Kemper, Claudia</creatorcontrib><creatorcontrib>Pirooznia, Mehdi</creatorcontrib><creatorcontrib>Laurence, Arian</creatorcontrib><creatorcontrib>Kordasti, Shahram</creatorcontrib><creatorcontrib>Kazemian, Majid</creatorcontrib><creatorcontrib>Lombardi, Giovanna</creatorcontrib><creatorcontrib>Afzali, Behdad</creatorcontrib><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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS 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>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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 Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Povoleri, Giovanni A. M.</au><au>Nova-Lamperti, Estefania</au><au>Scottà, Cristiano</au><au>Fanelli, Giorgia</au><au>Chen, Yun-Ching</au><au>Becker, Pablo D.</au><au>Boardman, Dominic</au><au>Costantini, Benedetta</au><au>Romano, Marco</au><au>Pavlidis, Polychronis</au><au>McGregor, Reuben</au><au>Pantazi, Eirini</au><au>Chauss, Daniel</au><au>Sun, Hong-Wei</au><au>Shih, Han-Yu</au><au>Cousins, David J.</au><au>Cooper, Nichola</au><au>Powell, Nick</au><au>Kemper, Claudia</au><au>Pirooznia, Mehdi</au><au>Laurence, Arian</au><au>Kordasti, Shahram</au><au>Kazemian, Majid</au><au>Lombardi, Giovanna</au><au>Afzali, Behdad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human retinoic acid–regulated CD161+ regulatory T cells support wound repair in intestinal mucosa</atitle><jtitle>Nature immunology</jtitle><stitle>Nat Immunol</stitle><addtitle>Nat Immunol</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>19</volume><issue>12</issue><spage>1403</spage><epage>1414</epage><pages>1403-1414</pages><issn>1529-2908</issn><eissn>1529-2916</eissn><abstract>Repair of tissue damaged during inflammatory processes is key to the return of local homeostasis and restoration of epithelial integrity. Here we describe CD161
+
regulatory T (T
reg
) cells as a distinct, highly suppressive population of T
reg
cells that mediate wound healing. These T
reg
cells were enriched in intestinal lamina propria, particularly in Crohn’s disease. CD161
+
T
reg
cells had an all-
trans
retinoic acid (ATRA)-regulated gene signature, and CD161 expression on T
reg
cells was induced by ATRA, which directly regulated the
CD161
gene. CD161 was co-stimulatory, and ligation with the T cell antigen receptor induced cytokines that accelerated the wound healing of intestinal epithelial cells. We identified a transcription-factor network, including BACH2, RORγt, FOSL2, AP-1 and RUNX1, that controlled expression of the wound-healing program, and found a CD161
+
T
reg
cell signature in Crohn’s disease mucosa associated with reduced inflammation. These findings identify CD161
+
T
reg
cells as a population involved in controlling the balance between inflammation and epithelial barrier healing in the gut.
T
reg
cells are essential for enforcing peripheral tolerance but can also influence tissue regeneration. Afzali and colleagues use high-dimensional analysis to describe a distinct population of CD161
+
human T
reg
cells involved in wound healing of the intestinal mucosa.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>30397350</pmid><doi>10.1038/s41590-018-0230-z</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-2968-1156</orcidid><orcidid>https://orcid.org/0000-0003-1980-1230</orcidid><orcidid>https://orcid.org/0000-0003-3821-9596</orcidid><orcidid>https://orcid.org/0000-0003-0342-651X</orcidid><orcidid>https://orcid.org/0000-0002-7525-5433</orcidid><oa>free_for_read</oa></addata></record> |
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ispartof | Nature immunology, 2018-12, Vol.19 (12), p.1403-1414 |
issn | 1529-2908 1529-2916 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6474659 |
source | MEDLINE; Nature; Alma/SFX Local Collection |
subjects | 631/250/1619/554/1898/1271 631/250/2152/569 Activator protein 1 Biomedical and Life Sciences Biomedicine Crohn Disease - immunology Crohn's disease Epithelial cells Homeostasis Humans Immunology Immunoregulation Infectious Diseases Inflammation Intestinal Mucosa - immunology Intestine Lamina propria Lymphocytes Lymphocytes T Mucosa NK Cell Lectin-Like Receptor Subfamily B - immunology Retinoic acid Runx1 protein T-Lymphocyte Subsets - immunology T-Lymphocytes, Regulatory - immunology Transcription factors Tretinoin - immunology Wound healing Wound Healing - immunology |
title | Human retinoic acid–regulated CD161+ regulatory T cells support wound repair in intestinal mucosa |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T18%3A06%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Human%20retinoic%20acid%E2%80%93regulated%20CD161+%20regulatory%20T%20cells%20support%20wound%20repair%20in%20intestinal%20mucosa&rft.jtitle=Nature%20immunology&rft.au=Povoleri,%20Giovanni%20A.%20M.&rft.date=2018-12-01&rft.volume=19&rft.issue=12&rft.spage=1403&rft.epage=1414&rft.pages=1403-1414&rft.issn=1529-2908&rft.eissn=1529-2916&rft_id=info:doi/10.1038/s41590-018-0230-z&rft_dat=%3Cproquest_pubme%3E2134280822%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2134280822&rft_id=info:pmid/30397350&rfr_iscdi=true |