<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Acurcio RC</submitter><funding>Fundação para a Ciência e a Tecnologia</funding><funding>"la Caixa" Foundation CaixaImpulse</funding><funding>ISIDORe project (ISID_c7f4) funded under HORIZON EUROPE</funding><funding>European Research Council</funding><funding>Fundação para a Ciência e Tecnologia-Ministério da Ciência</funding><funding>'la Caixa' Foundation</funding><funding>Israel Science Foundation</funding><funding>Tecnologia e Ensino Superior FCT-MCTES</funding><funding>Melanoma Research Alliance</funding><funding>&amp;apos;la Caixa&amp;apos; Foundation</funding><funding>Israel Cancer Research Fund</funding><pagination>e2404159</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11515909</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(40)</volume><pubmed_abstract>The first approved vaccines for human use against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are nanotechnology-based. Although they are modular, rapidly produced, and can reduce disease severity, the currently available vaccines are restricted in preventing infection, stressing the global demand for novel preventive vaccine technologies. Bearing this in mind, we set out to develop a flexible nanovaccine platform for nasal administration to induce mucosal immunity, which is fundamental for optimal protection against respiratory virus infection. The next-generation multiepitope nanovaccines co-deliver immunogenic peptides, selected by an immunoinformatic workflow, along with adjuvants and regulators of the PD-L1 expression. As a case study, we focused on SARS-CoV-2 peptide</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Intranasal Multiepitope PD-L1-siRNA-Based Nanovaccine: The Next-Gen COVID-19 Immunotherapy.</pubmed_title><pmcid>PMC11515909</pmcid><funding_grant_id>LCF/TR/CD20/52700005</funding_grant_id><funding_grant_id>EXPL/MED-QUI/1316/2021</funding_grant_id><funding_grant_id>1969/18</funding_grant_id><funding_grant_id>591187(ImmuNovation)</funding_grant_id><funding_grant_id>UIDB/04138/2020</funding_grant_id><funding_grant_id>835227</funding_grant_id><funding_grant_id>UIDP/04138/2020</funding_grant_id><funding_grant_id>PROF-18-682</funding_grant_id><funding_grant_id>PTDC/BTM-SAL/4350/2021</funding_grant_id><funding_grant_id>615808</funding_grant_id><funding_grant_id>CF01-00014</funding_grant_id><funding_grant_id>UTAP-EXPL/NPN/0041/2021</funding_grant_id><funding_grant_id>835227(3DBrainStrom)</funding_grant_id><funding_grant_id>SAICTCOVID/72538/2020</funding_grant_id><funding_grant_id>PROF‐18‐682</funding_grant_id><pubmed_authors>Freund NT</pubmed_authors><pubmed_authors>Yeheskel A</pubmed_authors><pubmed_authors>Yeini E</pubmed_authors><pubmed_authors>Kleiner R</pubmed_authors><pubmed_authors>Viana AS</pubmed_authors><pubmed_authors>Guerry C</pubmed_authors><pubmed_authors>Florindo HF</pubmed_authors><pubmed_authors>Mor M</pubmed_authors><pubmed_authors>Vaskovich-Koubi D</pubmed_authors><pubmed_authors>Palma C</pubmed_authors><pubmed_authors>Acurcio RC</pubmed_authors><pubmed_authors>Goncalves J</pubmed_authors><pubmed_authors>Fabregue M</pubmed_authors><pubmed_authors>Bacharach E</pubmed_authors><pubmed_authors>Aviel-Ronen S</pubmed_authors><pubmed_authors>Satchi-Fainaro R</pubmed_authors><pubmed_authors>Liubomirski Y</pubmed_authors><pubmed_authors>Araujo C</pubmed_authors><pubmed_authors>Matthieu S</pubmed_authors><pubmed_authors>Carreira B</pubmed_authors><pubmed_authors>Toister-Achituv M</pubmed_authors><pubmed_authors>Ferreira V</pubmed_authors><pubmed_authors>Zarubica A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intranasal Multiepitope PD-L1-siRNA-Based Nanovaccine: The Next-Gen COVID-19 Immunotherapy.</name><description>The first approved vaccines for human use against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are nanotechnology-based. Although they are modular, rapidly produced, and can reduce disease severity, the currently available vaccines are restricted in preventing infection, stressing the global demand for novel preventive vaccine technologies. Bearing this in mind, we set out to develop a flexible nanovaccine platform for nasal administration to induce mucosal immunity, which is fundamental for optimal protection against respiratory virus infection. The next-generation multiepitope nanovaccines co-deliver immunogenic peptides, selected by an immunoinformatic workflow, along with adjuvants and regulators of the PD-L1 expression. As a case study, we focused on SARS-CoV-2 peptide</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-07-15T14:45:45.312Z</modification><creation>2025-04-06T14:20:57.807Z</creation></dates><accession>S-EPMC11515909</accession><cross_references><pubmed>39116324</pubmed><doi>10.1002/advs.202404159</doi></cross_references></HashMap>