Toll‑like receptors ligand immunomodulators for the treatment congenital diaphragmatic hernia.
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Vallejo-Cremades, Mayte
Merino, Javier
Carmona-Mejías, Rita María
Córdoba, Laura
Salvador, Beatriz
Martínez, Leopoldo
Tovar, Juan Antonio
Llamas, Miguel Ángel
Muñoz-Chápuli-Oriol, Ramón
Fresno, Manuel
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Abstract
Congenital 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.
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Vallejo‑Cremades et al. Orphanet Journal of Rare Diseases (2024) 19:386 https://doi.org/10.1186/s13023-024-03384-7






