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Allergoid-mannan conjugates reprogram monocytes into tolerogenic dendritic cells via epigenetic and metabolic rewiring.
Benito-Villalvilla, Cristina; Pérez-Diego, Mario; Angelina, Alba; Kisand, Kai; Rebane, Ana; Subiza, José Luis; Palomares, Oscar.
Afiliação
  • Benito-Villalvilla C; Department of Biochemistry and Molecular Biology, School of Chemistry, Complutense University, Madrid, Spain.
  • Pérez-Diego M; Department of Biochemistry and Molecular Biology, School of Chemistry, Complutense University, Madrid, Spain.
  • Angelina A; Department of Biochemistry and Molecular Biology, School of Chemistry, Complutense University, Madrid, Spain.
  • Kisand K; Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
  • Rebane A; Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
  • Subiza JL; Inmunotek, Alcalá de Henares, Madrid, Spain.
  • Palomares O; Department of Biochemistry and Molecular Biology, School of Chemistry, Complutense University, Madrid, Spain. Electronic address: oscar.palomares@quim.ucm.es.
J Allergy Clin Immunol ; 149(1): 212-222.e9, 2022 01.
Article em En | MEDLINE | ID: mdl-34153371
ABSTRACT

BACKGROUND:

Allergoid-mannan conjugates are novel vaccines for allergen-specific immunotherapy being currently assayed in phase 2 clinical trials. Allergoid-mannan conjugates target dendritic cells (DCs) and generate functional forkhead box P3 (FOXP3)-positive Treg cells, but their capacity to reprogram monocyte differentiation remains unknown.

OBJECTIVE:

We studied whether allergoid-mannan conjugates could reprogram monocyte differentiation into tolerogenic DCs and the underlying molecular mechanisms.

METHODS:

Monocytes from nonatopic and allergic subjects were differentiated into DCs under conventional protocols in the absence or presence of allergoid-mannan conjugates. ELISA, real-time quantitative PCR, coculture, flow cytometry, and suppression assay were performed. Metabolic and epigenetic techniques were also used.

RESULTS:

Monocyte differentiation from nonatopic and allergic subjects into DCs in the presence of allergoid-mannan conjugates yields stable tolerogenic DCs. Lipopolysaccharide-stimulated mannan-tolDCs show a significantly lower cytokine production, lower TNF-α/IL-10 ratio, and higher expression of the tolerogenic molecules PDL1, IDO, SOCS1, SOCS3, and IL10; and they induce higher numbers of functional FOXP3+ Treg cells than conventional DC counterparts. Mannan-tolDCs shift glucose metabolism from Warburg effect and lactate production to mitochondrial oxidative phosphorylation. They also display epigenetic reprogramming involving specific histone marks within tolerogenic loci and lower expression levels of histone deacetylase genes. Mannan-tolDCs significantly increase the expression of the anti-inflammatory miRNA-146a/b and decrease proinflammatory miRNA-155.

CONCLUSIONS:

Allergoid-mannan conjugates reprogram monocyte differentiation into stable tolerogenic DCs via epigenetic and metabolic reprogramming. Our findings shed light on the novel mechanisms by which allergoid-mannan conjugates might contribute to allergen tolerance induction during allergen-specific immunotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Dendríticas / Monócitos / Alergoides / Mananas Tipo de estudo: Guideline Limite: Adult / Female / Humans / Male Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Dendríticas / Monócitos / Alergoides / Mananas Tipo de estudo: Guideline Limite: Adult / Female / Humans / Male Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2022 Tipo de documento: Article