<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Proietti, Michele</dc:creator>
  <dc:creator>Perruzza, Lisa</dc:creator>
  <dc:creator>Scribano, Daniela</dc:creator>
  <dc:creator>Pellegrini, Giovanni</dc:creator>
  <dc:creator>D’Antuono, Rocco</dc:creator>
  <dc:creator>Strati, Francesco</dc:creator>
  <dc:creator>Raffaelli, Marco</dc:creator>
  <dc:creator>Gonzalez, Santiago F.</dc:creator>
  <dc:creator>Thelen, Marcus</dc:creator>
  <dc:creator>Hardt, Wolf-Dietrich</dc:creator>
  <dc:creator>Slack, Emma</dc:creator>
  <dc:creator>Nicoletti, Mauro</dc:creator>
  <dc:creator>Grassi, Fabio</dc:creator>
  <dc:date>2019-01-16</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">T cell dependent secretory IgA (SIgA) generated in the Peyer’s patches (PPs) of the small intestine shapes a broadly diverse microbiota that is crucial for host physiology. The mutualistic  co-evolution of host and microbes led to the relative tolerance of host’s immune system towards commensal microorganisms. The ATP-gated ionotropic P2X7 receptor limits T follicular  helper (Tfh) cells expansion and germinal center (GC) reaction in the PPs. Here we show that transient depletion of intestinal ATP can dramatically improve high-affinity IgA response  against both live and inactivated oral vaccines. Ectopic expression of Shigella flexneri periplasmic ATP-diphosphohydrolase (apyrase) abolishes ATP release by bacteria and improves the  specific IgA response against live oral vaccines. Antibody responses primed in the absence of intestinal extracellular ATP (eATP) also provide superior protection from enteropathogenic  infection. Thus, modulation of eATP in the small intestine can affect highaffinity IgA response against gut colonizing bacteria.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://n2t.net/ark:/12658/srd1318837</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/318837</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318837/files/Proietti_NatCommun_2019.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-018-08156-z</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318837</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Nature Communications. - 2019, vol. 10, p. Art. number: 250</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Gastroenterology</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Mucosal immunology</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns3="xml" ns3:lang="en">ATP released by intestinal bacteria limits the generation of protective IgA against enteropathogens</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
