<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Miller LM</submitter><funding>NHLBI NIH HHS</funding><pagination>e188342</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12352901</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>135(16)</volume><pubmed_abstract>Influenza-associated bacterial superinfections in the lung lead to increased morbidity and mortality. Nearly all people have preexisting memory to influenza virus, which can protect against subsequent infection in the lung. This study explored the role B cells play in protection against bacterial (Staphylococcus aureus or Klebsiella pneumoniae) superinfection with previous heterotypic influenza memory. B cell deficiency resulted in an increased inflammatory lung environment and lung tissue injury during superinfection. Loss of B cells increased populations of memory CD8+ T cells in the lung, and these CD8+ T cells were transcriptionally and functionally distinct from those of WT mice. Use of antibody-deficient mouse models showed that this phenotype was specifically due to loss of antibody</pubmed_abstract><journal>The Journal of clinical investigation</journal><pubmed_title>B cell deficiency induces cytotoxic memory CD8+ T cells during influenza-associated bacterial pneumonia.</pubmed_title><pmcid>PMC12352901</pmcid><funding_grant_id>R01 HL107380</funding_grant_id><pubmed_authors>Gupta A</pubmed_authors><pubmed_authors>Alcorn JF</pubmed_authors><pubmed_authors>Cipolla EM</pubmed_authors><pubmed_authors>Miller LM</pubmed_authors><pubmed_authors>Dresden BP</pubmed_authors><pubmed_authors>Rago F</pubmed_authors><pubmed_authors>Parenteau KL</pubmed_authors><pubmed_authors>Duray AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>B cell deficiency induces cytotoxic memory CD8+ T cells during influenza-associated bacterial pneumonia.</name><description>Influenza-associated bacterial superinfections in the lung lead to increased morbidity and mortality. Nearly all people have preexisting memory to influenza virus, which can protect against subsequent infection in the lung. This study explored the role B cells play in protection against bacterial (Staphylococcus aureus or Klebsiella pneumoniae) superinfection with previous heterotypic influenza memory. B cell deficiency resulted in an increased inflammatory lung environment and lung tissue injury during superinfection. Loss of B cells increased populations of memory CD8+ T cells in the lung, and these CD8+ T cells were transcriptionally and functionally distinct from those of WT mice. Use of antibody-deficient mouse models showed that this phenotype was specifically due to loss of antibody</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-29T17:01:44.462Z</modification><creation>2026-04-08T05:25:23.935Z</creation></dates><accession>S-EPMC12352901</accession><cross_references><pubmed>40493422</pubmed><doi>10.1172/JCI188342</doi></cross_references></HashMap>