<?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>2026-04-18T06:13:51Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:20.500.12327/3054" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:20.500.12327/3054</identifier><datestamp>2025-10-22T11:09:15Z</datestamp><setSpec>com_2072_4428</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_487898</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Falcón, Ana</subfield>
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      <subfield code="a">Martínez-Pulgarín, Susana</subfield>
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      <subfield code="a">López-Serrano, Sergi</subfield>
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      <subfield code="a">Reytor, Edel</subfield>
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      <subfield code="a">Cid, Miguel</subfield>
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      <subfield code="a">Núñez, Maria del Carmen</subfield>
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      <subfield code="a">Córdoba, Lorena</subfield>
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      <subfield code="a">Darji, Ayub</subfield>
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      <subfield code="a">Escribano, José M.</subfield>
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      <subfield code="c">2024-05-23</subfield>
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      <subfield code="a">In this study, we pioneered an alternative technology for manufacturing subunit influenza&#xd;
hemagglutinin (HA)-based vaccines. This innovative method involves harnessing the pupae of the&#xd;
Lepidoptera Trichoplusia ni (T. ni) as natural biofactories in combination with baculovirus vectors&#xd;
(using CrisBio® technology). We engineered recombinant baculoviruses encoding two versions&#xd;
of the HA protein (trimeric or monomeric) derived from a pandemic avian H7N1 virus A strain&#xd;
(A/chicken/Italy/5093/99). These were then used to infect T. ni pupae, resulting in the production&#xd;
of the desired recombinant antigens. The obtained HA proteins were purified using affinity chromatography, consistently yielding approximately 75 mg/L of insect extract. The vaccine antigen&#xd;
effectively immunized poultry, which were subsequently challenged with a virulent H7N1 avian&#xd;
influenza virus. Following infection, all vaccinated animals survived without displaying any clinical&#xd;
symptoms, while none of the mock-vaccinated control animals survived. The CrisBio®-derived&#xd;
antigens induced high titers of HA-specific antibodies in the vaccinated poultry, demonstrating&#xd;
hemagglutination inhibition activity against avian H7N1 and human H7N9 viruses. These results&#xd;
suggest that the CrisBio® technology platform has the potential to address major industry challenges&#xd;
associated with producing recombinant influenza subunit vaccines, such as enhancing production&#xd;
yields, scalability, and the speed of development, facilitating the global deployment of highly effective&#xd;
influenza vaccines.</subfield>
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      <subfield code="a">Falcón, Ana, Susana Martínez-Pulgarín, Sergi López-Serrano, Edel Reytor, Miguel Cid, Maria Del Carmen Nuñez, Lorena Córdoba, Ayub Darji, and José M. Escribano. 2024. “Development of a Fully Protective Pandemic Avian Influenza Subunit Vaccine in Insect Pupae.” Viruses 16 (6): 829. https://doi.org/10.3390/v16060829.</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12327/3054</subfield>
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      <subfield code="a">https://doi.org/10.3390/v16060829</subfield>
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      <subfield code="a">Development of a Fully Protective Pandemic Avian Influenza Subunit Vaccine in Insect Pupae</subfield>
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