Role of the IL33 and IL1RL1 pathway in the pathogenesis of Immunoglobulin A vasculitis

dc.contributor.author
Prieto Peña, Diana
dc.contributor.author
Remuzgo Martínez, Sara
dc.contributor.author
Genre, Fernanda
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Pulito Cueto, Verónica
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Atienza Mateo, Belén
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Llorca Ballester, Jaime
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Sevilla Pérez, Belén
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Ortego Centeno, Norberto
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Marquez, Ana
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Lera Gómez, Leticia
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Leonardo, María Teresa
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Peñalba, Ana
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Narváez García, Francisco Javier
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Martín Penagos, Luis
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Rodrigo, Emilio
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Miranda Filloy, José A.
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Caminal Montero, Luis
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Collado, Paz
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Sánchez Pérez, Javier
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Argila, Diego de
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Rubio, Esteban
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León Luque, Manuel
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Blanco Madrigal, Juan María
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Galíndez Agirregoikoa, Eva
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Gualillo, Oreste
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Martín, Javier
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Castañeda, Santos
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Blanco, Ricardo
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González Gay, Miguel A.
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López Mejías, Raquel
dc.date.issued
2021-09-13T10:39:36Z
dc.date.issued
2021-09-13T10:39:36Z
dc.date.issued
2021-08-09
dc.date.issued
2021-09-10T07:21:41Z
dc.identifier
2045-2322
dc.identifier
https://hdl.handle.net/2445/179997
dc.identifier
34373564
dc.description.abstract
Cytokines signalling pathway genes are crucial factors of the genetic network underlying the pathogenesis of Immunoglobulin-A vasculitis (IgAV), an inflammatory vascular condition. An influence of the interleukin (IL)33- IL1 receptor like (IL1RL)1 signalling pathway on the increased risk of several immune-mediated diseases has been described. Accordingly, we assessed whether the IL33-IL1RL1 pathway represents a novel genetic risk factor for IgAV. Three tag polymorphisms within IL33 (rs3939286, rs7025417 and rs7044343) and three within IL1RL1 (rs2310173, rs13015714 and rs2058660), that also were previously associated with several inflammatory diseases, were genotyped in 380 Caucasian IgAV patients and 845 matched healthy controls. No genotypes or alleles differences were observed between IgAV patients and controls when IL33 and IL1RL1 variants were analysed independently. Likewise, no statistically significant differences were found in IL33 or IL1RL1 genotype and allele frequencies when IgAV patients were stratified according to the age at disease onset or to the presence/absence of gastrointestinal (GI) or renal manifestations. Similar results were disclosed when IL33 and IL1RL1 haplotypes were compared between IgAV patients and controls and between IgAV patients stratified according to the clinical characteristics mentioned above. Our results suggest that the IL33-IL1RL1 signalling pathway does not contribute to the genetic network underlying IgAV.
dc.format
8 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Springer Science and Business Media LLC
dc.relation
Reproducció del document publicat a: https://doi.org/10.1038/s41598-021-95762-5
dc.relation
Scientific Reports, 2021, vol. 11
dc.relation
https://doi.org/10.1038/s41598-021-95762-5
dc.relation
info:eu-repo/grantAgreement/EC/H2020/734899/EU//Olive-Net
dc.rights
cc by (c) Prieto Peña, Diana et al, 2021
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject
Malalties vasculars
dc.subject
Genètica mèdica
dc.subject
Vascular diseases
dc.subject
Medical genetics
dc.title
Role of the IL33 and IL1RL1 pathway in the pathogenesis of Immunoglobulin A vasculitis
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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