<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pido-Lopez J</submitter><funding>Wellcome Trust</funding><pagination>e1002396</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3228808</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(12)</volume><pubmed_abstract>The upper respiratory tract mucosa is the location for commensal Streptococcus (S.) pneumoniae colonization and therefore represents a major site of contact between host and bacteria. The CD4(+) T cell response to pneumococcus is increasingly recognised as an important mediator of immunity that protects against invasive disease, with data suggesting a critical role for Th17 cells in mucosal clearance. By assessing CD4 T cell proliferative responses we demonstrate age-related sequestration of Th1 and Th17 CD4(+) T cells reactive to pneumococcal protein antigens within mucosal lymphoid tissue. CD25(hi) T cell depletion and utilisation of pneumococcal specific MHCII tetramers revealed the presence of antigen specific Tregs that utilised CTLA-4 and PDL-1 surface molecules to suppress these res</pubmed_abstract><journal>PLoS pathogens</journal><pubmed_title>Acquisition of pneumococci specific effector and regulatory Cd4+ T cells localising within human upper respiratory-tract mucosal lymphoid tissue.</pubmed_title><pmcid>PMC3228808</pmcid><funding_grant_id>083603/B/07/Z</funding_grant_id><pubmed_authors>Heyderman RS</pubmed_authors><pubmed_authors>Kwok WW</pubmed_authors><pubmed_authors>Mitchell TJ</pubmed_authors><pubmed_authors>Pido-Lopez J</pubmed_authors><pubmed_authors>Williams NA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Acquisition of pneumococci specific effector and regulatory Cd4+ T cells localising within human upper respiratory-tract mucosal lymphoid tissue.</name><description>The upper respiratory tract mucosa is the location for commensal Streptococcus (S.) pneumoniae colonization and therefore represents a major site of contact between host and bacteria. The CD4(+) T cell response to pneumococcus is increasingly recognised as an important mediator of immunity that protects against invasive disease, with data suggesting a critical role for Th17 cells in mucosal clearance. By assessing CD4 T cell proliferative responses we demonstrate age-related sequestration of Th1 and Th17 CD4(+) T cells reactive to pneumococcal protein antigens within mucosal lymphoid tissue. CD25(hi) T cell depletion and utilisation of pneumococcal specific MHCII tetramers revealed the presence of antigen specific Tregs that utilised CTLA-4 and PDL-1 surface molecules to suppress these res</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Dec</publication><modification>2025-04-19T01:17:27.763Z</modification><creation>2019-03-27T00:46:37Z</creation></dates><accession>S-EPMC3228808</accession><cross_references><pubmed>22144893</pubmed><doi>10.1371/journal.ppat.1002396</doi></cross_references></HashMap>