<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Moffitt K</submitter><funding>NIAID NIH HHS</funding><pagination>909-16</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4519727</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(8)</volume><pubmed_abstract>A pneumococcal whole-cell vaccine (WCV) confers T(H)17-mediated immunogenicity and reduces nasopharyngeal (NP) carriage in mice. Activation of Toll-like receptor 2 (TLR2) has been shown to be important for generating T(H)17 responses, and several lipidated pneumococcal proteins have TLR2-activating properties. Here we investigated the roles of TLR2 and lipidation of proteins in WCV-induced interleukin-17A (IL-17A) responses and protection against NP carriage. Immunization of Tlr2(-/-) mice with WCV conferred significantly lower IL-17A levels and reduced protection against NP carriage, compared to wild-type (WT) mice, suggesting that host TLR2 engagement is required for effective immunity and protection elicited by WCV immunization. Using a WCV with deletion of lgt, the gene encoding the en</pubmed_abstract><journal>Clinical and vaccine immunology : CVI</journal><pubmed_title>T(H)17-Mediated Protection against Pneumococcal Carriage by a Whole-Cell Vaccine Is Dependent on Toll-Like Receptor 2 and Surface Lipoproteins.</pubmed_title><pmcid>PMC4519727</pmcid><funding_grant_id>R01 AI100114</funding_grant_id><funding_grant_id>K08 AI095352</funding_grant_id><funding_grant_id>K08-AI095352</funding_grant_id><funding_grant_id>R01-AI100114</funding_grant_id><pubmed_authors>Howard A</pubmed_authors><pubmed_authors>Basset A</pubmed_authors><pubmed_authors>Cheung E</pubmed_authors><pubmed_authors>Malley R</pubmed_authors><pubmed_authors>Moffitt K</pubmed_authors><pubmed_authors>Martin S</pubmed_authors><pubmed_authors>Herd M</pubmed_authors></additional><is_claimable>false</is_claimable><name>T(H)17-Mediated Protection against Pneumococcal Carriage by a Whole-Cell Vaccine Is Dependent on Toll-Like Receptor 2 and Surface Lipoproteins.</name><description>A pneumococcal whole-cell vaccine (WCV) confers T(H)17-mediated immunogenicity and reduces nasopharyngeal (NP) carriage in mice. Activation of Toll-like receptor 2 (TLR2) has been shown to be important for generating T(H)17 responses, and several lipidated pneumococcal proteins have TLR2-activating properties. Here we investigated the roles of TLR2 and lipidation of proteins in WCV-induced interleukin-17A (IL-17A) responses and protection against NP carriage. Immunization of Tlr2(-/-) mice with WCV conferred significantly lower IL-17A levels and reduced protection against NP carriage, compared to wild-type (WT) mice, suggesting that host TLR2 engagement is required for effective immunity and protection elicited by WCV immunization. Using a WCV with deletion of lgt, the gene encoding the en</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Aug</publication><modification>2025-04-19T07:49:06.965Z</modification><creation>2019-03-27T01:56:01Z</creation></dates><accession>S-EPMC4519727</accession><cross_references><pubmed>26041040</pubmed><doi>10.1128/CVI.00118-15</doi><doi>10.1128/cvi.00118-15</doi></cross_references></HashMap>