<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-18T07:10:10Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:20.500.12327/866" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:20.500.12327/866</identifier><datestamp>2025-10-22T11:00:04Z</datestamp><setSpec>com_2072_4428</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_487898</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Influenza NG-34 T cell conserved epitope adjuvanted with CAF01 as a possible influenza vaccine candidate</dc:title>
   <dc:creator>Sisteré-Oró, Marta</dc:creator>
   <dc:creator>Pedersen, Gabriel K.</dc:creator>
   <dc:creator>Córdoba, Lorena</dc:creator>
   <dc:creator>López-Serrano, Sergi</dc:creator>
   <dc:creator>Christensen, Dennis</dc:creator>
   <dc:creator>Darji, Ayub</dc:creator>
   <dc:contributor>Producció Animal</dc:contributor>
   <dc:contributor>Sanitat Animal</dc:contributor>
   <dc:subject>619</dc:subject>
   <dc:description>Conserved epitopes are targets commonly researched to be part of universal vaccine candidates against influenza viruses (IV). These conserved epitopes need to be cross-protecting against distinct IV subtypes and to have a strong immunogenic potential. Nevertheless, subunit vaccines generally require a strong adjuvant to enhance their immunological effects. Herewith, we compare four different adjuvants differing in their immunological signatures that may enhance efficacy of a conserved hemagglutinin (HA)-epitope from IV, the NG-34, to define the most efficient combination of antigen/adjuvant to combat IV infections. Soluble NG-34 was mixed with adjuvants like aluminium hydroxide (AH) and AddaVax, known to induce Th2 and humoral responses; CAF01 which displays a biased Th1/Th17 profile and Diluvac Forte which augments the humoral response. Combinations were tested in different groups of mice which were subjected to immunological analyses. CAF01 + NG-34 induced a complete immune response with the highest IgG1, IgG2c titers and percentages of activated CD4 T cell promoting IFN-γ, IL-2 and TNF-α producing cells. Furthermore, in NG-34 stimulated mice splenocytes, cytokine levels of IFN-γ, IL-1β, IL-6, IL-10, IL-17 and TNF-α were also the highest in the CAF01 + NG-34 mouse group. This complete induced immune response covering the humoral and the cellular arms of the adaptive immunity promoted by CAF01 + NG-34 group suggests that CAF01 could be a good candidate as an adjuvant to combine with NG-34 for an efficacious vaccine against IV. However, more studies performed in IV hosts as well as studies with a challenge model are further required.</dc:description>
   <dc:description>info:eu-repo/semantics/publishedVersion</dc:description>
   <dc:date>2020-04-20</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:identifier>Sisteré-Oró, Marta, Gabriel K. Pedersen, Lorena Córdoba, Sergi López-Serrano, Dennis Christensen, and Ayub Darji. 2020. "Influenza NG-34 T Cell Conserved Epitope Adjuvanted With CAF01 As A Possible Influenza Vaccine Candidate". Veterinary Research 51 (1). doi:10.1186/s13567-020-00770-4.</dc:identifier>
   <dc:identifier>0928-4249</dc:identifier>
   <dc:identifier>http://hdl.handle.net/20.500.12327/866</dc:identifier>
   <dc:identifier>https://doi.org/10.1186/s13567-020-00770-4</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Veterinary Research</dc:relation>
   <dc:relation>EC/H2020/730964/ES/European Vaccine Research and Development Infrastructure/TRANSVAC2</dc:relation>
   <dc:relation>MINECO/Programa estatal de I+D+I orientada a los retos de la sociedad/AGL2013-48923-C2-2-R/ES/Nuevas estrategias vacunales frente a enfermedades víricas ganaderas empleando pseudopartículas virales modificadas/</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>11</dc:format>
   <dc:publisher>BMC</dc:publisher>
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