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dc.contributor.authorSaubi, Cristina
dc.contributor.authorMeade, Kieran G.
dc.contributor.authorTravé-Asensio, Sergi
dc.contributor.authorGarcia-Fruitos, Elena
dc.contributor.authorArís, Anna
dc.contributor.otherProducció Animalca
dc.date.accessioned2026-03-20T10:46:10Z
dc.date.available2026-03-20T10:46:10Z
dc.date.issued2026-01-14
dc.identifier.issn1746-6148ca
dc.identifier.urihttps://hdl.handle.net/20.500.12327/5165
dc.description.abstractBackground Maintaining immune homeostasis is essential for livestock health and productivity, particularly in the face of infection or stress. Host defense peptides (HDPs), including β-defensins and cathelicidins, are key innate immune components with both antimicrobial and immunomodulatory properties. This study aimed to characterize the immunomodulatory effects of five bovine HDPs—BNBD1, BNBD3, LAP, Bac5, and BMAP27—on peripheral blood mononuclear cells (PBMCs) and bovine turbinate (BT) epithelial cells, under both basal and lipopolysaccharide (LPS)-stimulated inflammatory conditions. Cytokine secretion, cell viability, and real-time epithelial cell behavior were assessed to evaluate peptide-specific immune modulation. Results Under non-stimulated conditions, LAP stimulated the secretion of IL-8 (LAP p < 0.0001). In LPS-stimulated PBMCs, prophylactic HDP treatment (4 h pre-LPS) amplified inflammatory cytokine secretion. BNBD3 and LAP significantly increased IL-1β, IL-6, TNF-α, IFN-γ (p < 0.05), and chemokines such as IL-8 and MIP-1α (p < 0.01), suggesting an immune-priming effect that may enhance responsiveness to subsequent LPS stimulation. Notably, BNBD3 and LAP failed to induce a comparable inflammation when added 0.5 h after LPS, highlighting the context-dependent nature of HDP action. Conversely, BMAP27 demonstrated anti-inflammatory activity by reducing LPS-induced IL-1β, IFN-γ, and IL-10 (p < 0.001), irrespective of timing. Bac5 increased IL-8 secretion (p < 0.001) and MCP-1 (p < 0.05), suggesting a chemotactic effect. Cell viability assays confirmed that none of the peptides exhibited cytotoxicity in PBMCs at tested concentrations, although BMAP27 reduced lymphocyte numbers (40% decrease, p < 0.0001), possibly indicating selective immunoregulatory effects. In BT cells, Bac5 enhanced proliferation (11% increase, p < 0.05), while BNBD1 (23% decrease, p < 0.01) and BMAP27 (10% decrease, p < 0.05) mildly reduced cellular impedance, reflecting divergent impacts on epithelial dynamics. Conclusions These findings reveal distinct immunomodulatory profiles among bovine HDPs, ranging from pro-inflammatory (BNBD3, LAP) to suppressive (BMAP27), and underscore the importance of treatment timing. The immune-priming capacity of certain HDPs suggests potential use as prophylactic agents to enhance resilience to infections, while suppressive peptides like BMAP27 may serve therapeutic roles in resolving excessive inflammation. Importantly, the variability observed among individual animals emphasizes the need for personalized approaches in immunomodulation. Overall, this study provides novel insights into the immunological functions of bovine HDPs, supporting their potential as alternatives or adjunctive therapies to antibiotics in veterinary medicine.ca
dc.description.sponsorshipThis research was funded by MICIU/AEI/https://doi.org/10.13039/501100011033, grant number PID2022-136521OB-I00. C.S. was supported with a pre-doctoral fellowship from Generalitat de Catalunya (FI-AGAUR). The authors are also indebted to AGAUR for project 2021 SGR 01552. The authors are indebted to CERCA Programme (Generalitat de Catalunya) and the European Social Fund for supporting our research.
dc.format.extent13ca
dc.language.isoengca
dc.publisherBioMed Centralca
dc.relation.ispartofBMC Veterinary Researchca
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleImmunomodulatory activities of bovine host defense peptides (HDPs): context-dependent roles in inflammation and immune primingca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDESF/ / /EU/ /ca
dc.subject.udc612ca
dc.identifier.doihttps://doi.org/10.1186/s12917-025-05258-xca
dc.contributor.groupProducció de Remugantsca


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Attribution-NonCommercial-NoDerivatives 4.0 International
Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by-nc-nd/4.0/
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