Publication:
LPS promotes Th2 dependent sensitisation leading to anaphylaxis in a Pru p 3 mouse model.

dc.contributor.authorRodriguez, Maria J
dc.contributor.authorAranda, Ana
dc.contributor.authorFernandez, Tahia D
dc.contributor.authorCubells-Baeza, Nuria
dc.contributor.authorTorres, Maria J
dc.contributor.authorGomez, Francisca
dc.contributor.authorPalomares, Francisca
dc.contributor.authorPerkins, James R
dc.contributor.authorRojo, Javier
dc.contributor.authorDiaz-Perales, Araceli
dc.contributor.authorMayorga, Cristobalina
dc.date.accessioned2024-01-23T20:12:18Z
dc.date.available2024-01-23T20:12:18Z
dc.date.issued2017-01-13
dc.description.abstractPru p 3 is the major peach allergen in the Mediterranean area. It frequently elicits severe reactions, limiting its study in humans, raising the need for animal models to investigate the immunological mechanisms involved. However, no anaphylaxis model exists for Pru p 3. We aimed to develop a model of peach anaphylaxis by sensitising mice with Pru p 3 in combination with lipopolysaccharide (LPS) as an adjuvant. Four groups of mice were sensitised intranasally: untreated; treated with Pru p 3; treated with LPS; treated with Pru p 3 + LPS. After sensitisation mice were intraperitoneally challenged with Pru p 3 and in vivo and in vitro parameters were evaluated. Only mice in the Pru p 3 + LPS group showed anaphylaxis symptoms, including a decrease in temperature. Determination of in vitro parameters showed a Th2 response with an increase of Pru p 3-specific IgE and IgG1. Moreover, at the cellular level, we found increased levels of IgE and IgG1 secreting Pru p 3-specific cells and a proliferative CD4+ T-cell response. These results demonstrate that Pru p 3-specific anaphylaxis can be generated after nasal sensitisation to Pru p 3 in combination with LPS. This is a promising model for evaluating food allergy immunotherapies.
dc.format.page40449es_ES
dc.format.volume7es_ES
dc.identifier.doi10.1038/srep40449
dc.identifier.e-issn2045-2322es_ES
dc.identifier.journalScientific reportses_ES
dc.identifier.otherhttp://hdl.handle.net/10668/10771
dc.identifier.pubmedID28084419es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17280
dc.language.isoeng
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAnaphylaxis
dc.subject.meshAnimals
dc.subject.meshAntibodies
dc.subject.meshAntibody Specificity
dc.subject.meshAntigens, Plant
dc.subject.meshCell Proliferation
dc.subject.meshDisease Models, Animal
dc.subject.meshEnzyme-Linked Immunospot Assay
dc.subject.meshFemale
dc.subject.meshImmunization
dc.subject.meshImmunoglobulin E
dc.subject.meshImmunoglobulin G
dc.subject.meshLipopolysaccharides
dc.subject.meshMice, Inbred BALB C
dc.subject.meshSpleen
dc.titleLPS promotes Th2 dependent sensitisation leading to anaphylaxis in a Pru p 3 mouse model.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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