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dc.contributor.authorDelgado-Bonet, Pablo
dc.contributor.authorArias-Pulido, Hugo
dc.contributor.authorCastillo Magan, Noemí del
dc.contributor.authorZimmermann, Anna Barbara Emilia
dc.contributor.authorSchaafsma, Evelien
dc.contributor.authorVom Berg, Johannes
dc.contributor.authorVázquez, Fernando
dc.contributor.authorBeiss, Veronique
dc.contributor.authorSteinmetz, Nicole F.
dc.contributor.authorFiering, Steven
dc.contributor.authorPerisé-Barrios, Ana Judith
dc.date.accessioned2026-09-09T11:11:32Z
dc.date.available2026-09-09T11:11:32Z
dc.date.issued2025
dc.identifier.citationDelgado-Bonet, P., Arias-Pulido, H., del Castillo Magan, N., Emilia Zimmermann, A. B., Schaafsma, E., Vom Berg, J., ... & Perise-Barrios, A. J. (2025). Pilot study of intratumoral immunotherapy with cowpea mosaic virus nanoparticles: safety in refractory canine oral tumors. Molecular Pharmaceutics, 22(5), 2671-2683. https://doi.org/10.1021/acs.molpharmaceut.5c00100es
dc.identifier.issn1543-8384
dc.identifier.issn1543-8392
dc.identifier.otherhttps://pubs.acs.org/mpohbp/article/22/5/2671/3750137/Pilot-Study-of-Intratumoral-Immunotherapy-withes
dc.identifier.urihttp://hdl.handle.net/20.500.12020/2079
dc.description.abstractOraltumors(squamouscellcarcinoma,malignant melanoma, and fibrosarcoma) represent 6−7% of all canine cancers. Given that these tumors have a high local recurrence rate and metastatic potential, conventional therapies have suboptimal response rates, leading to poor patient outcomes. Here, we report the use of intratumoral virus-like particles from cowpea mosaic virus (CPMV) in four canine patients with recurrent oral malignant tumors and lymph node metastasis. All tumors were nonresponders to chemotherapy and had a mild initial response to CPMV intratumoral immunotherapy without any serious immune-related adverse effects. None of the patients developed pulmonary metastasis during follow-up, although local progression was seen in all the patients. Furthermore, tumor-infiltrated immune T cells increased in number after the intratumoral immunotherapy with CPMV, suggesting activation of the tumor microenvironment. All the patients had a rapid decrease in the tumor-promoting chemokines IL-8 and CXCL1, which could indicate that a decrease in metastatic potential could have been generated by the CPMV immunotherapy. The increased number of infiltrated immune cells, the decrease in some pro-tumoral chemokines, and the absence of adverse effects suggest that CPMV could be a safe treatment and should be further explored as a novel therapy for canine oral tumors.es
dc.language.isoenes
dc.publisherACS Publicationses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titlePilot Study of Intratumoral Immunotherapy with Cowpea Mosaic Virus Nanoparticles: Safety in Refractory Canine Oral Tumorses
dc.typearticlees
dc.identifier.doihttps://doi.org/10.1021/acs.molpharmaceut.5c00100
dc.issue.number5es
dc.journal.titleMolecular Pharmaceuticses
dc.page.initial2671es
dc.page.final2683es
dc.relation.projectID1.010.909; 1.013.001; NCI: U01CA218292; R01CA224605; 5P30CA023108; 1S10OD030242; P20GM130454; KFS-4146-02-2017es
dc.rights.accessRightsopenAccesses
dc.subject.areaBiología Celular y Moleculares
dc.subject.areaCiencias Biomédicases
dc.subject.keywordCPMVes
dc.subject.keywordIntratumoral immunotherapyes
dc.subject.keywordOral canine tumorses
dc.subject.keywordVirus-like particleses
dc.subject.keywordNanoparticleses
dc.subject.keywordMalignant oral melanomaes
dc.subject.unesco32 Ciencias Médicases
dc.volume.number22es


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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