Toll‑like receptors ligand immunomodulators for the treatment congenital diaphragmatic hernia.

dc.centroFacultad de Medicinaes_ES
dc.contributor.authorVallejo-Cremades, Mayte
dc.contributor.authorMerino, Javier
dc.contributor.authorCarmona-Mejías, Rita María
dc.contributor.authorCórdoba, Laura
dc.contributor.authorSalvador, Beatriz
dc.contributor.authorMartínez, Leopoldo
dc.contributor.authorTovar, Juan Antonio
dc.contributor.authorLlamas, Miguel Ángel
dc.contributor.authorMuñoz-Chápuli-Oriol, Ramón
dc.contributor.authorFresno, Manuel
dc.date.accessioned2025-06-13T09:04:57Z
dc.date.available2025-06-13T09:04:57Z
dc.date.created2024
dc.date.issued2024
dc.departamentoAnatomía Humana, Medicina Legal e Historia de la Cienciaes_ES
dc.description.abstractCongenital diaphragmatic hernia (CDH) is a rare disease that affects the development of the diaphragm, leading to abnormal lung development. Unfortunately, there is no established therapy for CDH. Retinoic acid pathways are implicated in the ethology of CDH and macrophages are known to play a role in repairing organ damage. We have analyzed the effect of several Toll like receptor (TLR) ligands in the nitrofen-induced CDH model in pregnant rats widely used to study this disease and in the G2-GATA4Cre;Wt1fl/fl CDH genetic mice model. Morphometric and histological studies were carried out. Immune cell infiltration was assayed by immunochemistry and immunofluorescence and retinoic pathway gene expression analyzed in vivo and in vitro in macrophages. Our research has shown that TLR ligand immunomodulators that influence anti-inflammatory macrophage activation can be effective in treating CDH, being nontoxic for the mothers or pups suggesting that those TLR ligands are a promising solution for CDH leading to orphan drug designation for CS1. The immune system of the fetus would be responsible for repairing the damage and closure of the hernia in the diaphragm and enhanced proper lung development after CS1 treatment.es_ES
dc.identifier.citationVallejo‑Cremades et al. Orphanet Journal of Rare Diseases (2024) 19:386 https://doi.org/10.1186/s13023-024-03384-7es_ES
dc.identifier.doi10.1186/s13023-024-03384-7
dc.identifier.urihttps://hdl.handle.net/10630/38984
dc.language.isoenges_ES
dc.publisherBMCes_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectCardiopatía congénitaes_ES
dc.subjectCorazón - Embriologíaes_ES
dc.subjectGenética del desarrolloes_ES
dc.subjectMacrófagoses_ES
dc.subjectInteracción celulares_ES
dc.subject.otherFetal therapyes_ES
dc.subject.otherToll-like receptorses_ES
dc.subject.otherMacrophageses_ES
dc.subject.otherInflammationes_ES
dc.subject.otherRetinoic pathwayes_ES
dc.subject.otherEmbryonic developmentes_ES
dc.subject.otherCongenital diaphragmatic herniaes_ES
dc.subject.otherOrphan druges_ES
dc.titleToll‑like receptors ligand immunomodulators for the treatment congenital diaphragmatic hernia.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication206a58ce-6491-4719-be84-31826b30ba43
relation.isAuthorOfPublicationa7809911-0927-46bc-be1a-efa2dcdf6858
relation.isAuthorOfPublication.latestForDiscovery206a58ce-6491-4719-be84-31826b30ba43

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