IL-37 is a fundamental inhibitor of innate immunity
The function of IL-37 remains elusive. Dinarello and colleagues find that IL-37 acts as a natural suppressor of innate inflammatory and immune responses. The function of interleukin 37 (IL-37; formerly IL-1 family member 7) has remained elusive. Expression of IL-37 in macrophages or epithelial cells...
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Veröffentlicht in: | Nature immunology 2010-11, Vol.11 (11), p.1014-1022 |
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creator | Nold, Marcel F Nold-Petry, Claudia A Zepp, Jarod A Palmer, Brent E Bufler, Philip Dinarello, Charles A |
description | The function of IL-37 remains elusive. Dinarello and colleagues find that IL-37 acts as a natural suppressor of innate inflammatory and immune responses.
The function of interleukin 37 (IL-37; formerly IL-1 family member 7) has remained elusive. Expression of IL-37 in macrophages or epithelial cells almost completely suppressed production of pro-inflammatory cytokines, whereas the abundance of these cytokines increased with silencing of endogenous IL-37 in human blood cells. Anti-inflammatory cytokines were unaffected. Mice with transgenic expression of IL-37 were protected from lipopolysaccharide-induced shock, and showed markedly improved lung and kidney function and reduced liver damage after treatment with lipopolysaccharide. Transgenic mice had lower concentrations of circulating and tissue cytokines (72–95% less) than wild-type mice and showed less dendritic cell activation. IL-37 interacted intracellularly with Smad3 and IL-37-expressing cells and transgenic mice showed less cytokine suppression when endogenous Smad3 was depleted. IL-37 thus emerges as a natural suppressor of innate inflammatory and immune responses. |
doi_str_mv | 10.1038/ni.1944 |
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The function of interleukin 37 (IL-37; formerly IL-1 family member 7) has remained elusive. Expression of IL-37 in macrophages or epithelial cells almost completely suppressed production of pro-inflammatory cytokines, whereas the abundance of these cytokines increased with silencing of endogenous IL-37 in human blood cells. Anti-inflammatory cytokines were unaffected. Mice with transgenic expression of IL-37 were protected from lipopolysaccharide-induced shock, and showed markedly improved lung and kidney function and reduced liver damage after treatment with lipopolysaccharide. Transgenic mice had lower concentrations of circulating and tissue cytokines (72–95% less) than wild-type mice and showed less dendritic cell activation. IL-37 interacted intracellularly with Smad3 and IL-37-expressing cells and transgenic mice showed less cytokine suppression when endogenous Smad3 was depleted. IL-37 thus emerges as a natural suppressor of innate inflammatory and immune responses.</description><identifier>ISSN: 1529-2908</identifier><identifier>EISSN: 1529-2916</identifier><identifier>DOI: 10.1038/ni.1944</identifier><identifier>PMID: 20935647</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/250/127/1213 ; 631/250/262 ; 631/250/516 ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Cell Line ; Dendritic cells ; Gene Knockdown Techniques ; Humans ; Immunity, Innate - immunology ; Immunology ; Infectious Diseases ; Interleukin-1 - genetics ; Interleukin-1 - immunology ; Interleukins ; Kidneys ; Macrophages ; Mice ; Mice, Transgenic ; Physiological aspects ; Signal Transduction ; Smad3 Protein - immunology</subject><ispartof>Nature immunology, 2010-11, Vol.11 (11), p.1014-1022</ispartof><rights>Springer Nature America, Inc. 2010</rights><rights>COPYRIGHT 2010 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Nov 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-1760dd6eb1a5a945e00b327d34251a105ce2ef89f9fbdd274d836dfef1bed3ac3</citedby><cites>FETCH-LOGICAL-c506t-1760dd6eb1a5a945e00b327d34251a105ce2ef89f9fbdd274d836dfef1bed3ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/ni.1944$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/ni.1944$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20935647$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nold, Marcel F</creatorcontrib><creatorcontrib>Nold-Petry, Claudia A</creatorcontrib><creatorcontrib>Zepp, Jarod A</creatorcontrib><creatorcontrib>Palmer, Brent E</creatorcontrib><creatorcontrib>Bufler, Philip</creatorcontrib><creatorcontrib>Dinarello, Charles A</creatorcontrib><title>IL-37 is a fundamental inhibitor of innate immunity</title><title>Nature immunology</title><addtitle>Nat Immunol</addtitle><addtitle>Nat Immunol</addtitle><description>The function of IL-37 remains elusive. Dinarello and colleagues find that IL-37 acts as a natural suppressor of innate inflammatory and immune responses.
The function of interleukin 37 (IL-37; formerly IL-1 family member 7) has remained elusive. Expression of IL-37 in macrophages or epithelial cells almost completely suppressed production of pro-inflammatory cytokines, whereas the abundance of these cytokines increased with silencing of endogenous IL-37 in human blood cells. Anti-inflammatory cytokines were unaffected. Mice with transgenic expression of IL-37 were protected from lipopolysaccharide-induced shock, and showed markedly improved lung and kidney function and reduced liver damage after treatment with lipopolysaccharide. Transgenic mice had lower concentrations of circulating and tissue cytokines (72–95% less) than wild-type mice and showed less dendritic cell activation. IL-37 interacted intracellularly with Smad3 and IL-37-expressing cells and transgenic mice showed less cytokine suppression when endogenous Smad3 was depleted. IL-37 thus emerges as a natural suppressor of innate inflammatory and immune responses.</description><subject>631/250/127/1213</subject><subject>631/250/262</subject><subject>631/250/516</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Line</subject><subject>Dendritic cells</subject><subject>Gene Knockdown Techniques</subject><subject>Humans</subject><subject>Immunity, Innate - immunology</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Interleukin-1 - genetics</subject><subject>Interleukin-1 - immunology</subject><subject>Interleukins</subject><subject>Kidneys</subject><subject>Macrophages</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Physiological aspects</subject><subject>Signal Transduction</subject><subject>Smad3 Protein - immunology</subject><issn>1529-2908</issn><issn>1529-2916</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</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>eNqF0VtrFDEUB_AgFntR_AYy6IP2YdbcM_NYitWFhULV55CZnKwpM5maZKD99mbctbJFkDzk9ssJfw5CrwleEcyaj8GvSMv5M3RCBG1r2hL5_HGNm2N0mtItxoQryV-gY4pbJiRXJ4itNzVTlU-VqdwcrBkhZDNUPvzwnc9TrCZXNsFkqPw4zsHnh5foyJkhwav9fIa-X336dvml3lx_Xl9ebOpeYJlroiS2VkJHjDAtF4Bxx6iyjFNBDMGiBwquaV3rOmup4rZh0jpwpAPLTM_O0Ptd3bs4_ZwhZT361MMwmADTnHQjpJJKUfJfqUQrKCVykW-fyNtpjqHEWBARRFFV0Lsd2poBtA9uytH0S0l9QTnmjWp-f7r6hyrDwuj7KYDz5fzgwfnBg2Iy3OetmVPS6683h3afqI9TShGcvot-NPFBE6yXluvg9dLyIt_sE83dCPbR_elxAR92IJWrsIX4N_LTWr8Abjeu3Q</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>Nold, Marcel F</creator><creator>Nold-Petry, Claudia A</creator><creator>Zepp, Jarod A</creator><creator>Palmer, Brent E</creator><creator>Bufler, Philip</creator><creator>Dinarello, Charles A</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>ISR</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>AEUYN</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>RC3</scope><scope>7X8</scope></search><sort><creationdate>20101101</creationdate><title>IL-37 is a fundamental inhibitor of innate immunity</title><author>Nold, Marcel F ; Nold-Petry, Claudia A ; Zepp, Jarod A ; Palmer, Brent E ; Bufler, Philip ; Dinarello, Charles A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-1760dd6eb1a5a945e00b327d34251a105ce2ef89f9fbdd274d836dfef1bed3ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>631/250/127/1213</topic><topic>631/250/262</topic><topic>631/250/516</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Line</topic><topic>Dendritic cells</topic><topic>Gene Knockdown Techniques</topic><topic>Humans</topic><topic>Immunity, Innate - 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Academic</collection><jtitle>Nature immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nold, Marcel F</au><au>Nold-Petry, Claudia A</au><au>Zepp, Jarod A</au><au>Palmer, Brent E</au><au>Bufler, Philip</au><au>Dinarello, Charles A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IL-37 is a fundamental inhibitor of innate immunity</atitle><jtitle>Nature immunology</jtitle><stitle>Nat Immunol</stitle><addtitle>Nat Immunol</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>11</volume><issue>11</issue><spage>1014</spage><epage>1022</epage><pages>1014-1022</pages><issn>1529-2908</issn><eissn>1529-2916</eissn><abstract>The function of IL-37 remains elusive. Dinarello and colleagues find that IL-37 acts as a natural suppressor of innate inflammatory and immune responses.
The function of interleukin 37 (IL-37; formerly IL-1 family member 7) has remained elusive. Expression of IL-37 in macrophages or epithelial cells almost completely suppressed production of pro-inflammatory cytokines, whereas the abundance of these cytokines increased with silencing of endogenous IL-37 in human blood cells. Anti-inflammatory cytokines were unaffected. Mice with transgenic expression of IL-37 were protected from lipopolysaccharide-induced shock, and showed markedly improved lung and kidney function and reduced liver damage after treatment with lipopolysaccharide. Transgenic mice had lower concentrations of circulating and tissue cytokines (72–95% less) than wild-type mice and showed less dendritic cell activation. IL-37 interacted intracellularly with Smad3 and IL-37-expressing cells and transgenic mice showed less cytokine suppression when endogenous Smad3 was depleted. IL-37 thus emerges as a natural suppressor of innate inflammatory and immune responses.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>20935647</pmid><doi>10.1038/ni.1944</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/250/127/1213 631/250/262 631/250/516 Animals Biomedical and Life Sciences Biomedicine Cell Line Dendritic cells Gene Knockdown Techniques Humans Immunity, Innate - immunology Immunology Infectious Diseases Interleukin-1 - genetics Interleukin-1 - immunology Interleukins Kidneys Macrophages Mice Mice, Transgenic Physiological aspects Signal Transduction Smad3 Protein - immunology |
title | IL-37 is a fundamental inhibitor of innate immunity |
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