Abstract |
Intestinal microfold cells are the primary pathway for translocation of secretory IgA ( SIgA)-pathogen complexes to gut-associated lymphoid tissue. Uptake of SIgA/commensals complexes is important for priming adaptive immunity in the mucosa. This study aims to explore the effect of SIgA retrograde transport of immune complexes in Crohn's disease (CD). Here we report a significant increase of SIgA transport in CD patients with NOD2-mutation compared to CD patients without NOD2 mutation and/or healthy individuals. NOD2 has an effect in the IgA transport through human and mouse M cells by downregulating Dectin-1 and Siglec-5 expression, two receptors involved in retrograde transport. These findings define a mechanism of NOD2-mediated regulation of mucosal responses to intestinal microbiota, which is involved in CD intestinal inflammation and dysbiosis.
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Authors | Nicolas Rochereau, Xavier Roblin, Eva Michaud, Rémi Gayet, Blandine Chanut, Fabienne Jospin, Blaise Corthésy, Stéphane Paul |
Journal | Nature communications
(Nat Commun)
Vol. 12
Issue 1
Pg. 261
(01 11 2021)
ISSN: 2041-1723 [Electronic] England |
PMID | 33431850
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Immunoglobulin A, Secretory
- Lectins, C-Type
- Nod2 Signaling Adaptor Protein
- Sialic Acid Binding Immunoglobulin-like Lectins
- Siglecf protein, mouse
- dectin 1
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Topics |
- Animals
- Colitis
(microbiology, pathology)
- Crohn Disease
(metabolism, pathology)
- Humans
- Immunoglobulin A, Secretory
(metabolism)
- Lectins, C-Type
(metabolism)
- Mice, Knockout
- Models, Biological
- Mutation
(genetics)
- Nod2 Signaling Adaptor Protein
(deficiency, genetics, metabolism)
- Peyer's Patches
(metabolism)
- Protein Transport
- Salmonella
(physiology)
- Sialic Acid Binding Immunoglobulin-like Lectins
(metabolism)
- Transcytosis
- Mice
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