<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>Lindestam Arlehamn, Cecilia S.</dc:creator>
  <dc:creator>Paul, Sinu</dc:creator>
  <dc:creator>Mele, Federico</dc:creator>
  <dc:creator>Huang, Charlie</dc:creator>
  <dc:creator>Greenbaum, Jason A.</dc:creator>
  <dc:creator>Vita, Randi</dc:creator>
  <dc:creator>Sidney, John</dc:creator>
  <dc:creator>Peters, Bjoern</dc:creator>
  <dc:creator>Sallusto, Federica</dc:creator>
  <dc:creator>Sette, Alessandro</dc:creator>
  <dc:date>2014-12-29</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">A previous unbiased genome-wide analysis of CD4 Mycobacterium tuberculosis (MTB)  recognition using peripheral blood mononuclear cells from individuals with latent MTB  infection (LTBI) or nonexposed healthy controls (HCs) revealed that certain MTB  sequences were unexpectedly recognized by HCs. In the present study, it was found  that, based on their pattern of reactivity, epitopes could be divided into LTBI-specific,  mixed reactivity, and HC-specific categories. This pattern corresponded to sequence  conservation in nontuberculous mycobacteria (NTMs), suggesting environmental  exposure as an underlying cause of differential reactivity. LTBI-specific epitopes were  found to be hyperconserved, as previously reported, whereas the opposite was true for  NTM conserved epitopes, suggesting that intragenus conservation also influences host  pathogen adaptation. The biological relevance of this observation was demonstrated  further by several observations. First, the T cells elicited by MTB/NTM cross-reactive  epitopes in HCs were found mainly in a CCR6+CXCR3+ memory subset, similar to  findings in LTBI individuals. Thus, both MTB and NTM appear to elicit a phenotypically  similar T-cell response. Second, T cells reactive to MTB/NTM-conserved epitopes  responded to naturally processed epitopes from MTB and NTMs, whereas T cells  reactive to MTB-specific epitopes responded only to MTB. Third, cross-reactivity could  be translated to antigen recognition. Several MTB candidate vaccine antigens were  cross-reactive, but others were MTB-specific. Finally, NTM-specific epitopes that elicit  T cells that recognize NTMs but not MTB were identified. These epitopes can be used  to characterize T-cell responses to NTMs, eliminating the confounding factor of MTB  cross-recognition and providing insights into vaccine design and evaluation.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/319030</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1319030</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319030/files/Lindestam_PNAS_2015.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.1416537112</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319030</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Proceedings of the national academy of sciences of the United States of America. - 2015, vol. 112, no. 2, p. E147-E155</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Tuberculosis</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">T-cell epitope</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">NTM</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Epitope conservation</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">T-cell subset</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Immunological consequences of intragenus conservation of Mycobacterium tuberculosis T-cell epitopes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
