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The oral commensal Streptococcus mitis shows a mixed memory Th cell signature that is similar to and cross-reactive with Streptococcus pneumoniae
Carriage of and infection with Streptococcus pneumoniae is known to predominantly induce T helper 17 (Th17) responses in humans, but the types of Th cells showing reactivity towards commensal streptococci with low pathogenic potential, such as the oral commensals S. mitis and S. salivarius, remain u...
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Published in: | PloS one 2014-08, Vol.9 (8), p.e104306-e104306 |
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description | Carriage of and infection with Streptococcus pneumoniae is known to predominantly induce T helper 17 (Th17) responses in humans, but the types of Th cells showing reactivity towards commensal streptococci with low pathogenic potential, such as the oral commensals S. mitis and S. salivarius, remain uncharacterized.
Memory CD4(+) T helper (Th) cell subsets were isolated from healthy human blood donors according to differential expression of chemokine receptors, expanded in vitro using polyclonal stimuli and characterized for reactivity against different streptococcal strains.
Th cells responding to S. mitis, S. salivarius and S. pneumoniae were predominantly in a CCR6(+)CXCR3(+) subset and produced IFN-γ, and in a CCR6(+)CCR4(+) subset and produced IL-17 and IL-22. Frequencies of S. pneumoniae-reactive Th cells were higher than frequencies of S. mitis- and S. salivarius-specific Th cells. S. mitis and S. pneumoniae isogenic capsule knock-out mutants and a S. mitis mutant expressing the serotype 4 capsule of S. pneumoniae showed no different Th cell responses as compared to wild type strains. S. mitis-specific Th17 cells showed cross-reactivity with S. pneumoniae.
As Th17 cells partly control clearance of S. pneumoniae, cross-reactive Th17 cells that may be induced by commensal bacterial species may influence the immune response, independent of capsule expression. |
doi_str_mv | 10.1371/journal.pone.0104306 |
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Memory CD4(+) T helper (Th) cell subsets were isolated from healthy human blood donors according to differential expression of chemokine receptors, expanded in vitro using polyclonal stimuli and characterized for reactivity against different streptococcal strains.
Th cells responding to S. mitis, S. salivarius and S. pneumoniae were predominantly in a CCR6(+)CXCR3(+) subset and produced IFN-γ, and in a CCR6(+)CCR4(+) subset and produced IL-17 and IL-22. Frequencies of S. pneumoniae-reactive Th cells were higher than frequencies of S. mitis- and S. salivarius-specific Th cells. S. mitis and S. pneumoniae isogenic capsule knock-out mutants and a S. mitis mutant expressing the serotype 4 capsule of S. pneumoniae showed no different Th cell responses as compared to wild type strains. S. mitis-specific Th17 cells showed cross-reactivity with S. pneumoniae.
As Th17 cells partly control clearance of S. pneumoniae, cross-reactive Th17 cells that may be induced by commensal bacterial species may influence the immune response, independent of capsule expression.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0104306</identifier><identifier>PMID: 25119879</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Antigens ; Bacterial infections ; Biology ; Biology and life sciences ; Blood & organ donations ; Blood donation ; Blood donors ; CCR6 protein ; CD4 antigen ; Chemokine receptors ; Commensals ; Cross Reactions - immunology ; Cross-reactivity ; CXCR3 protein ; Cytokines ; Health aspects ; Health care ; Helper cells ; Humans ; Immune clearance ; Immune response ; Immune system ; Interferon ; Interferon-gamma - immunology ; Interleukin 17 ; Interleukin 22 ; Interleukin-17 - immunology ; Interleukins - immunology ; Lymphocytes ; Lymphocytes T ; Medicine and Health Sciences ; Mouth - microbiology ; Mutants ; Pneumonia ; Reactivity ; Receptors ; Research and Analysis Methods ; Strains (organisms) ; Streptococcus infections ; Streptococcus mitis ; Streptococcus mitis - immunology ; Streptococcus pneumoniae ; Streptococcus pneumoniae - immunology ; T-Lymphocytes, Helper-Inducer - immunology ; γ-Interferon</subject><ispartof>PloS one, 2014-08, Vol.9 (8), p.e104306-e104306</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Engen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>info:eu-repo/semantics/openAccess</rights><rights>2014 Engen et al 2014 Engen et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c716t-82a4373b4c214570cef47f2478665138b981a4e6081d2b2aaef3b399e37f8bc63</citedby><cites>FETCH-LOGICAL-c716t-82a4373b4c214570cef47f2478665138b981a4e6081d2b2aaef3b399e37f8bc63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1553137189/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1553137189?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,26566,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25119879$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Beall, Bernard</contributor><creatorcontrib>Engen, Stian André</creatorcontrib><creatorcontrib>Valen Rukke, Håkon</creatorcontrib><creatorcontrib>Becattini, Simone</creatorcontrib><creatorcontrib>Jarrossay, David</creatorcontrib><creatorcontrib>Blix, Inger Johanne</creatorcontrib><creatorcontrib>Petersen, Fernanda Cristina</creatorcontrib><creatorcontrib>Sallusto, Federica</creatorcontrib><creatorcontrib>Schenck, Karl</creatorcontrib><title>The oral commensal Streptococcus mitis shows a mixed memory Th cell signature that is similar to and cross-reactive with Streptococcus pneumoniae</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Carriage of and infection with Streptococcus pneumoniae is known to predominantly induce T helper 17 (Th17) responses in humans, but the types of Th cells showing reactivity towards commensal streptococci with low pathogenic potential, such as the oral commensals S. mitis and S. salivarius, remain uncharacterized.
Memory CD4(+) T helper (Th) cell subsets were isolated from healthy human blood donors according to differential expression of chemokine receptors, expanded in vitro using polyclonal stimuli and characterized for reactivity against different streptococcal strains.
Th cells responding to S. mitis, S. salivarius and S. pneumoniae were predominantly in a CCR6(+)CXCR3(+) subset and produced IFN-γ, and in a CCR6(+)CCR4(+) subset and produced IL-17 and IL-22. Frequencies of S. pneumoniae-reactive Th cells were higher than frequencies of S. mitis- and S. salivarius-specific Th cells. S. mitis and S. pneumoniae isogenic capsule knock-out mutants and a S. mitis mutant expressing the serotype 4 capsule of S. pneumoniae showed no different Th cell responses as compared to wild type strains. S. mitis-specific Th17 cells showed cross-reactivity with S. pneumoniae.
As Th17 cells partly control clearance of S. pneumoniae, cross-reactive Th17 cells that may be induced by commensal bacterial species may influence the immune response, independent of capsule expression.</description><subject>Antigens</subject><subject>Bacterial infections</subject><subject>Biology</subject><subject>Biology and life sciences</subject><subject>Blood & organ donations</subject><subject>Blood donation</subject><subject>Blood donors</subject><subject>CCR6 protein</subject><subject>CD4 antigen</subject><subject>Chemokine receptors</subject><subject>Commensals</subject><subject>Cross Reactions - immunology</subject><subject>Cross-reactivity</subject><subject>CXCR3 protein</subject><subject>Cytokines</subject><subject>Health aspects</subject><subject>Health care</subject><subject>Helper cells</subject><subject>Humans</subject><subject>Immune clearance</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Interferon</subject><subject>Interferon-gamma - immunology</subject><subject>Interleukin 17</subject><subject>Interleukin 22</subject><subject>Interleukin-17 - immunology</subject><subject>Interleukins - immunology</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Medicine and Health Sciences</subject><subject>Mouth - microbiology</subject><subject>Mutants</subject><subject>Pneumonia</subject><subject>Reactivity</subject><subject>Receptors</subject><subject>Research and Analysis Methods</subject><subject>Strains (organisms)</subject><subject>Streptococcus infections</subject><subject>Streptococcus mitis</subject><subject>Streptococcus mitis - immunology</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - immunology</subject><subject>T-Lymphocytes, Helper-Inducer - immunology</subject><subject>γ-Interferon</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>3HK</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9tu1DAQhiMEoqXwBggsISG42CU-JHFukKqKQ6VKlejCrTXxTjauEntrOz08Bm-MQ7dlt-oFykUc55t_PP94suw1zeeUV_TTuRu9hX6-dhbnOc0Fz8sn2T6tOZuVLOdPt9Z72YsQzvO84LIsn2d7rKC0llW9n_1edEich55oNwxoQ1qdRY_r6LTTegxkMNEEEjp3FQikr2tckgEH52_IoiMa-54Es7IQR48kdhDJhJvB9OBJdATskmjvQph5BB3NJZIrE7sHWdYWx8FZA_gye9ZCH_DV5n2Q_fz6ZXH0fXZy-u346PBkpitaxplkIHjFG6EZFUWVa2xF1TJRpQoLymVTSwoCy1zSJWsYALa84XWNvGplo0t-kL291V33LqiNm0HRouCTv7JOxPEtsXRwrtbeDOBvlAOj_m44v1Lgo9E9KlnKJM10UyIVggJoUUKFWmrGykZC0vq8yTY2Ay412phM3xHd_WNNp1buUgnKqZT833G1NyEaq2zqmqK5LJgSvBBFIj5sUnh3MWKIajBh6g9YdONtZRWlrKwS-u4B-nj9G2oFqURjW5dOpidRdSioLApWlJOP80eo9CxxMDpdztak_Z2AjzsBiYl4HVcwhqCOz378P3v6a5d9v8V2CH3sguvHaJwNu6C4szJdS4_tfRtorqba79xQ02ypzWylsDfbLbwPuhsm_gdyOR9o</recordid><startdate>20140813</startdate><enddate>20140813</enddate><creator>Engen, Stian André</creator><creator>Valen Rukke, Håkon</creator><creator>Becattini, Simone</creator><creator>Jarrossay, David</creator><creator>Blix, Inger Johanne</creator><creator>Petersen, Fernanda Cristina</creator><creator>Sallusto, Federica</creator><creator>Schenck, Karl</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</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>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>3HK</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140813</creationdate><title>The oral commensal Streptococcus mitis shows a mixed memory Th cell signature that is similar to and cross-reactive with Streptococcus pneumoniae</title><author>Engen, Stian André ; Valen Rukke, Håkon ; Becattini, Simone ; Jarrossay, David ; Blix, Inger Johanne ; Petersen, Fernanda Cristina ; Sallusto, Federica ; Schenck, Karl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c716t-82a4373b4c214570cef47f2478665138b981a4e6081d2b2aaef3b399e37f8bc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antigens</topic><topic>Bacterial infections</topic><topic>Biology</topic><topic>Biology and life sciences</topic><topic>Blood & organ donations</topic><topic>Blood donation</topic><topic>Blood donors</topic><topic>CCR6 protein</topic><topic>CD4 antigen</topic><topic>Chemokine receptors</topic><topic>Commensals</topic><topic>Cross Reactions - immunology</topic><topic>Cross-reactivity</topic><topic>CXCR3 protein</topic><topic>Cytokines</topic><topic>Health aspects</topic><topic>Health care</topic><topic>Helper cells</topic><topic>Humans</topic><topic>Immune clearance</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Interferon</topic><topic>Interferon-gamma - immunology</topic><topic>Interleukin 17</topic><topic>Interleukin 22</topic><topic>Interleukin-17 - immunology</topic><topic>Interleukins - immunology</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Medicine and Health Sciences</topic><topic>Mouth - microbiology</topic><topic>Mutants</topic><topic>Pneumonia</topic><topic>Reactivity</topic><topic>Receptors</topic><topic>Research and Analysis Methods</topic><topic>Strains (organisms)</topic><topic>Streptococcus infections</topic><topic>Streptococcus mitis</topic><topic>Streptococcus mitis - immunology</topic><topic>Streptococcus pneumoniae</topic><topic>Streptococcus pneumoniae - 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Academic</collection><collection>NORA - Norwegian Open Research Archives</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Engen, Stian André</au><au>Valen Rukke, Håkon</au><au>Becattini, Simone</au><au>Jarrossay, David</au><au>Blix, Inger Johanne</au><au>Petersen, Fernanda Cristina</au><au>Sallusto, Federica</au><au>Schenck, Karl</au><au>Beall, Bernard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The oral commensal Streptococcus mitis shows a mixed memory Th cell signature that is similar to and cross-reactive with Streptococcus pneumoniae</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-08-13</date><risdate>2014</risdate><volume>9</volume><issue>8</issue><spage>e104306</spage><epage>e104306</epage><pages>e104306-e104306</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Carriage of and infection with Streptococcus pneumoniae is known to predominantly induce T helper 17 (Th17) responses in humans, but the types of Th cells showing reactivity towards commensal streptococci with low pathogenic potential, such as the oral commensals S. mitis and S. salivarius, remain uncharacterized.
Memory CD4(+) T helper (Th) cell subsets were isolated from healthy human blood donors according to differential expression of chemokine receptors, expanded in vitro using polyclonal stimuli and characterized for reactivity against different streptococcal strains.
Th cells responding to S. mitis, S. salivarius and S. pneumoniae were predominantly in a CCR6(+)CXCR3(+) subset and produced IFN-γ, and in a CCR6(+)CCR4(+) subset and produced IL-17 and IL-22. Frequencies of S. pneumoniae-reactive Th cells were higher than frequencies of S. mitis- and S. salivarius-specific Th cells. S. mitis and S. pneumoniae isogenic capsule knock-out mutants and a S. mitis mutant expressing the serotype 4 capsule of S. pneumoniae showed no different Th cell responses as compared to wild type strains. S. mitis-specific Th17 cells showed cross-reactivity with S. pneumoniae.
As Th17 cells partly control clearance of S. pneumoniae, cross-reactive Th17 cells that may be induced by commensal bacterial species may influence the immune response, independent of capsule expression.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25119879</pmid><doi>10.1371/journal.pone.0104306</doi><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Bacterial infections Biology Biology and life sciences Blood & organ donations Blood donation Blood donors CCR6 protein CD4 antigen Chemokine receptors Commensals Cross Reactions - immunology Cross-reactivity CXCR3 protein Cytokines Health aspects Health care Helper cells Humans Immune clearance Immune response Immune system Interferon Interferon-gamma - immunology Interleukin 17 Interleukin 22 Interleukin-17 - immunology Interleukins - immunology Lymphocytes Lymphocytes T Medicine and Health Sciences Mouth - microbiology Mutants Pneumonia Reactivity Receptors Research and Analysis Methods Strains (organisms) Streptococcus infections Streptococcus mitis Streptococcus mitis - immunology Streptococcus pneumoniae Streptococcus pneumoniae - immunology T-Lymphocytes, Helper-Inducer - immunology γ-Interferon |
title | The oral commensal Streptococcus mitis shows a mixed memory Th cell signature that is similar to and cross-reactive with Streptococcus pneumoniae |
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