<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE123977" accession="SRP173648">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP173648</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA510410</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE123977</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Recurrent Group A Streptococcus Tonsillitis</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>To determine differences in GC Tfh cells isolated from the tonsils of children who have undergone tonsillectomy for either recurrent Group A Streptococcus (GAS) tonsillitis (RT) or non-RT (sleep apnea). Grants: Thrasher Research Fund for an Early Career Award 12969 - Jennifer Dan UM1 AI100663 - Shane Crotty Clinical Research Fellowship Grant UK Charity No. 1089464 - David Layfield, Ramsey Cuttress, Christian Ottensmeier Overall design: Tonsillar cells were isolated from 5 RT and 5 non-RT children. Cells were left unstimulated or stimulated with GAS or recombinant streptococcal pyrogenic exotoxin A (SpeA), a critical GAS virulence factor. Cells cultured for 18 hours. Cells were sorted for GC Tfh cells (CXCR5hiPD-1hiof CD45RA-CD4+T cells) using the Activation Induced Marker (AIM) assay. For unstimulated cells, CD25-OX40-GC Tfh cells were sorted. For GAS-specific or SpeA-responsive GC Tfh cells, CD25+OX40+GC Tfh cells were sorted. All cells were sorted into RNA lysis buffer. All data are derived from GC Tfh cells.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE123977</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>30728285</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
