<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>Mele, Federico</dc:creator>
  <dc:creator>Fornara, Chiara</dc:creator>
  <dc:creator>Jarrossay, David</dc:creator>
  <dc:creator>Furione, Milena</dc:creator>
  <dc:creator>Arossa, Alessia</dc:creator>
  <dc:creator>Spinillo, Arsenio</dc:creator>
  <dc:creator>Lanzavecchia, Antonio</dc:creator>
  <dc:creator>Gerna, Giuseppe</dc:creator>
  <dc:creator>Sallusto, Federica</dc:creator>
  <dc:creator>Lilleri, Daniele</dc:creator>
  <dc:date>2017-11-07</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Congenital human cytomegalovirus (HCMV) infection is the major cause of birth defects and a precise  definition of the HCMV-specific T-cell response in primary infection may help define reliable correlates of  immune protection during pregnancy. In this study, a high throughput method was used to define the  frequency of CD4+ and CD8+ T cells specific for four HCMV proteins in the naïve compartment of  seronegative subjects and the effector/memory compartments of subjects with primary/remote HCMV  infection. The naïve repertoire displayed comparable frequencies of T cells that were reactive with HCMV  structural (pp65, gB and the pentamer gHgLpUL128L) and non-structural (IE-1) proteins. Whereas,  following natural infection, the majority of effector/memory CD4+ and CD8+ T cells recognized either gB  or IE-1, respectively, and pp65. The pattern of T cell reactivity was comparable at early and late stages of  infection and in pregnant women with primary HCMV infection transmitting or not transmitting the virus to  the fetus. At an early stage of primary infection, about 50% of HCMV-reactive CD4+ T cells were long- term IL-7Rpos memory cells, while 6–12 months later, the frequency of these cells increased to 70%,  approaching 100% in remote infections. In contrast, only 10–20% of HCMV-specific CD8+ T cells were  long-term memory cells up to 12 months after infection onset, thereafter increasing to 70% in remote  infections. Interestingly, a significantly higher frequency of HCMV-specific CD4+ T cells with a long-term  IL-7Rpos memory phenotype was observed in non-transmitting compared to transmitting women. These  findings indicate that immunodominance in HCMV infection is not predetermined in the naïve  compartment, but is the result of virus-host interactions and suggest that prompt control of HCMV  infection in pregnancy is associated with the rapid development of long-term IL-7Rpos memory HCMV- specific CD4+ T cells and a low risk of virus transmission to the fetus.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://n2t.net/ark:/12658/srd1319049</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/319049</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319049/files/Mele_PO_2017.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0187731</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319049</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Plos one. - 2017, vol. 12, no. 11, p. e0187731</dc:source>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Phenotype and specificity of T cells in primary human cytomegalovirus infection during pregnancy : IL-7Rpos long-term memory phenotype is associated with protection from vertical transmission</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_5794</dc:type>
</oai_dc:dc>
