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Commonly invasive serotypes of Streptococcus pneumoniae trigger a reduced innate immune response compared with serotypes rarely responsible for invasive infection
Although there are more than 90 serotypes of Streptococcus pneumoniae (or pneumococcus), it is not understood why a small number of serotypes account for most invasive infections. To investigate the human innate immune response triggered by different pneumococcal serotypes, monocyte-derived macropha...
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Published in: | FEMS immunology and medical microbiology 2008-06, Vol.53 (1), p.136-139 |
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creator | Burgess, Thomas S.T Hirschfeld, Aaron F Tyrrell, Gregory J Bettinger, Julie A Turvey, Stuart E |
description | Although there are more than 90 serotypes of Streptococcus pneumoniae (or pneumococcus), it is not understood why a small number of serotypes account for most invasive infections. To investigate the human innate immune response triggered by different pneumococcal serotypes, monocyte-derived macrophages were exposed to a group of commonly and rarely invasive pneumococcal clinical isolates and tumor necrosis factor (TNF)-α production was measured. Commonly invasive pneumococcal serotypes triggered significantly less TNF-α production than serotypes rarely responsible for invasive infection (P |
doi_str_mv | 10.1111/j.1574-695X.2008.00382.x |
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To investigate the human innate immune response triggered by different pneumococcal serotypes, monocyte-derived macrophages were exposed to a group of commonly and rarely invasive pneumococcal clinical isolates and tumor necrosis factor (TNF)-α production was measured. Commonly invasive pneumococcal serotypes triggered significantly less TNF-α production than serotypes rarely responsible for invasive infection (P<0.004). These data indicate that one factor influencing the invasive potential of a pneumococcal serotype is the magnitude of innate immune-mediated TNF-α production triggered by exposure to the organism and suggest that the integrated host response generated against commonly invasive pneumococcal serotypes may be less effective than the response directed against rarely invasive serotypes.</description><identifier>ISSN: 0928-8244</identifier><identifier>EISSN: 1574-695X</identifier><identifier>EISSN: 2049-632X</identifier><identifier>DOI: 10.1111/j.1574-695X.2008.00382.x</identifier><identifier>PMID: 18248437</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Adolescent ; Bacteriology ; Biological and medical sciences ; Cell Line ; Child ; Child, Preschool ; Clinical isolates ; Enzyme-Linked Immunosorbent Assay ; Fundamental and applied biological sciences. Psychology ; Human behavior ; Humans ; Immune response ; Immune system ; immunity ; Immunity, Innate - immunology ; Infant ; Innate immunity ; Macrophages ; Macrophages - immunology ; Macrophages - microbiology ; Microbiology ; Miscellaneous ; Monocytes ; Pneumococcal Infections - immunology ; Pneumococcal Infections - microbiology ; pneumococcus ; Serotypes ; Streptococcus infections ; Streptococcus pneumoniae ; Streptococcus pneumoniae - immunology ; Streptococcus pneumoniae - pathogenicity ; TNF-α ; Tumor Necrosis Factor-alpha - immunology ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α ; Vaccines</subject><ispartof>FEMS immunology and medical microbiology, 2008-06, Vol.53 (1), p.136-139</ispartof><rights>2008 Federation of European Microbiological Societies 2008</rights><rights>2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. 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To investigate the human innate immune response triggered by different pneumococcal serotypes, monocyte-derived macrophages were exposed to a group of commonly and rarely invasive pneumococcal clinical isolates and tumor necrosis factor (TNF)-α production was measured. Commonly invasive pneumococcal serotypes triggered significantly less TNF-α production than serotypes rarely responsible for invasive infection (P<0.004). 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Psychology</subject><subject>Human behavior</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>immunity</subject><subject>Immunity, Innate - immunology</subject><subject>Infant</subject><subject>Innate immunity</subject><subject>Macrophages</subject><subject>Macrophages - immunology</subject><subject>Macrophages - microbiology</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Monocytes</subject><subject>Pneumococcal Infections - immunology</subject><subject>Pneumococcal Infections - microbiology</subject><subject>pneumococcus</subject><subject>Serotypes</subject><subject>Streptococcus infections</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - immunology</subject><subject>Streptococcus pneumoniae - pathogenicity</subject><subject>TNF-α</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><subject>Vaccines</subject><issn>0928-8244</issn><issn>1574-695X</issn><issn>2049-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkc9u1DAQxiMEoqXwCmAJwS2L_8SxI3GpVhQqFXEolbhZXmeyeJXYwU7a7uvwpMyyqxYhEPhie_z7ZsbzFQVhdMFwvdksmFRVWTfyy4JTqheUCs0Xtw-K47uHh8UxbbguNa-qo-JJzhtKadVQ-rg4YhjUlVDHxfdlHIYY-i3x4dpmfw0kQ4rTdoRMYkcupwTjFF10bs5kDDAj7S2QKfn1GhKxJEE7O2gxQbATED8McwCM5jGGDMTFYbTIkBs_ff0lecIglj1wftUD6WK6b8OHDtzkY3haPOpsn-HZYT8prs7efV5-KC8-vT9fnl6UTnLBS-nalsFKAZPaAigFwjpgSmoc0KprmNWMy4aqzoHm0lYtXqUVyspW6saJk-L1Pu-Y4rcZ8mQGnx30vQ0Q52zqBkctK_ZPkNNKal7XCL78DdzEOQX8hOGC1lwpWSuk9J5yKeacoDNj8oNNW8Oo2dltNmbnqtm5anZ2m592m1uUPj8UmFcDtPfCg78IvDoANjvbd8kG5_Mdx6moOKs0cm_33I3vYfvfDZiz8494QLnYy-M8_kVc_qn7F3tVZ6Ox64SNXV1yygRCjeBKiB8JweLP</recordid><startdate>200806</startdate><enddate>200806</enddate><creator>Burgess, Thomas S.T</creator><creator>Hirschfeld, Aaron F</creator><creator>Tyrrell, Gregory J</creator><creator>Bettinger, Julie A</creator><creator>Turvey, Stuart E</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Oxford University Press</general><scope>FBQ</scope><scope>IQODW</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>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7QL</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200806</creationdate><title>Commonly invasive serotypes of Streptococcus pneumoniae trigger a reduced innate immune response compared with serotypes rarely responsible for invasive infection</title><author>Burgess, Thomas S.T ; Hirschfeld, Aaron F ; Tyrrell, Gregory J ; Bettinger, Julie A ; Turvey, Stuart E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5232-5cdd1eb7e158aee77e3ace1758008bf91a8125907fce825a4d1255a37a5d589c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Clinical isolates</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Human behavior</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immune system</topic><topic>immunity</topic><topic>Immunity, Innate - immunology</topic><topic>Infant</topic><topic>Innate immunity</topic><topic>Macrophages</topic><topic>Macrophages - immunology</topic><topic>Macrophages - microbiology</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Monocytes</topic><topic>Pneumococcal Infections - immunology</topic><topic>Pneumococcal Infections - microbiology</topic><topic>pneumococcus</topic><topic>Serotypes</topic><topic>Streptococcus infections</topic><topic>Streptococcus pneumoniae</topic><topic>Streptococcus pneumoniae - immunology</topic><topic>Streptococcus pneumoniae - pathogenicity</topic><topic>TNF-α</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Burgess, Thomas S.T</creatorcontrib><creatorcontrib>Hirschfeld, Aaron F</creatorcontrib><creatorcontrib>Tyrrell, Gregory J</creatorcontrib><creatorcontrib>Bettinger, Julie A</creatorcontrib><creatorcontrib>Turvey, Stuart E</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS immunology and medical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Burgess, Thomas S.T</au><au>Hirschfeld, Aaron F</au><au>Tyrrell, Gregory J</au><au>Bettinger, Julie A</au><au>Turvey, Stuart E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Commonly invasive serotypes of Streptococcus pneumoniae trigger a reduced innate immune response compared with serotypes rarely responsible for invasive infection</atitle><jtitle>FEMS immunology and medical microbiology</jtitle><addtitle>FEMS Immunol Med Microbiol</addtitle><date>2008-06</date><risdate>2008</risdate><volume>53</volume><issue>1</issue><spage>136</spage><epage>139</epage><pages>136-139</pages><issn>0928-8244</issn><eissn>1574-695X</eissn><eissn>2049-632X</eissn><abstract>Although there are more than 90 serotypes of Streptococcus pneumoniae (or pneumococcus), it is not understood why a small number of serotypes account for most invasive infections. 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subjects | Adolescent Bacteriology Biological and medical sciences Cell Line Child Child, Preschool Clinical isolates Enzyme-Linked Immunosorbent Assay Fundamental and applied biological sciences. Psychology Human behavior Humans Immune response Immune system immunity Immunity, Innate - immunology Infant Innate immunity Macrophages Macrophages - immunology Macrophages - microbiology Microbiology Miscellaneous Monocytes Pneumococcal Infections - immunology Pneumococcal Infections - microbiology pneumococcus Serotypes Streptococcus infections Streptococcus pneumoniae Streptococcus pneumoniae - immunology Streptococcus pneumoniae - pathogenicity TNF-α Tumor Necrosis Factor-alpha - immunology Tumor necrosis factor-TNF Tumor necrosis factor-α Vaccines |
title | Commonly invasive serotypes of Streptococcus pneumoniae trigger a reduced innate immune response compared with serotypes rarely responsible for invasive infection |
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