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Combining different bacteria in vaccine formulations enhances the chance for antiviral cross-reactive immunity: a detailed in silico analysis for influenza A virus

dc.contributor.authorBodas Pinedo, Andrés
dc.contributor.authorLafuente Duarte, María Esther
dc.contributor.authorPeláez Prestel, Héctor Fernando
dc.contributor.authorRas Carmona, Álvaro
dc.contributor.authorSubiza Garrido-Lestache, José Luis
dc.contributor.authorReche Gallardo, Pedro Antonio
dc.date.accessioned2025-01-27T07:55:37Z
dc.date.available2025-01-27T07:55:37Z
dc.date.issued2023-08-22
dc.description.abstractBacteria are well known to provide heterologous immunity against viral infections through various mechanisms including the induction of innate trained immunity and adaptive cross-reactive immunity. Cross-reactive immunity from bacteria to viruses is responsible for long-term protection and yet its role has been downplayed due the difficulty of determining antigen-specific responses. Here, we carried out a systematic evaluation of the potential cross-reactive immunity from selected bacteria known to induce heterologous immunity against various viruses causing recurrent respiratory infections. The bacteria selected in this work were Bacillus Calmette Guerin and those included in the poly-bacterial preparation MV130: Streptococcus pneumoniae, Staphylococcus aureus, Staphylococcus epidermidis, Klebisella pneumoniae, Branhamella catarrhalis and Haemophilus influenzae. The virus included influenza A and B viruses, human rhinovirus A, B and C, respiratory syncytial virus A and B and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Through BLAST searches, we first identified the shared peptidome space (identity ≥ 80%, in at least 8 residues) between bacteria and viruses, and subsequently predicted T and B cell epitopes within shared peptides. Interestingly, the potential epitope spaces shared between bacteria in MV130 and viruses are non-overlapping. Hence, combining diverse bacteria can enhance cross-reactive immunity. We next analyzed in detail the cross-reactive T and B cell epitopes between MV130 and influenza A virus. We found that MV130 contains numerous cross-reactive T cell epitopes with high population protection coverage and potentially neutralizing B cell epitopes recognizing hemagglutinin and matrix protein 2. These results contribute to explain the immune enhancing properties of MV130 observed in the clinic against respiratory viral infections.
dc.description.departmentDepto. de Inmunología, Oftalmología y ORL
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.sponsorshipUniversidad Complutense de Madrid
dc.description.sponsorshipInmunotek
dc.description.statuspub
dc.identifier.citationBodas-Pinedo, A., Lafuente, E. M., Pelaez-Prestel, H. F., Ras-Carmona, A., Subiza, J. L., & Reche, P. A. (2023). Combining different bacteria in vaccine formulations enhances the chance for antiviral cross-reactive immunity: a detailed in silico analysis for influenza A virus. Frontiers in immunology, 14, 1235053. https://doi.org/10.3389/fimmu.2023.1235053
dc.identifier.doi10.3389/fimmu.2023.1235053
dc.identifier.issn1664-3224
dc.identifier.officialurlhttps://doi.org/10.3389/fimmu.2023.1235053
dc.identifier.pmid37675108
dc.identifier.relatedurlhttps://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1235053/full#h8
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/37675108/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/116132
dc.journal.titleFrontiers in immunology
dc.language.isoeng
dc.page.initial1235053
dc.publisherFrontiers
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu612.017
dc.subject.keywordMV130
dc.subject.keywordBacteria
dc.subject.keywordcross-reactivity
dc.subject.keywordEpitope
dc.subject.keywordInfluenza A virus
dc.subject.keywordRespiratory viruses
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmMedicina
dc.subject.ucmInmunología
dc.subject.unesco24 Ciencias de la Vida
dc.subject.unesco2412 Inmunología
dc.titleCombining different bacteria in vaccine formulations enhances the chance for antiviral cross-reactive immunity: a detailed in silico analysis for influenza A virus
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number14
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery905af5c7-75ed-4e1a-a643-3cc365b6b809

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