Enrichment of human IgA-coated bacterial vesicles in ulcerative colitis as a driver of inflammation

The gut microbiome contributes to chronic inflammatory responses in ulcerative colitis (UC), but molecular mechanisms and disease-relevant effectors remain unclear. Here we analyze the pro-inflammatory properties of colonic fluid obtained during colonoscopy from UC and control patients. In patients with UC, we find that the pelletable effector fraction is composed mostly of bacterial extracellular vesicles (BEVs) that exhibit high IgA-levels and incite strong pro-inflammatory responses in IgA receptor-positive (CD89<sup>+</sup>) immune cells. Biopsy analyses reveal higher infiltration of CD89<sup>+</sup> immune cells in the colonic mucosa from patients with UC than control individuals. Further studies show that IgA-coated BEVs, but not host-derived vesicles nor soluble IgA, are potent activators of pro-inflammatory responses in CD89<sup>+</sup> cells. IgA-coated BEVs also exacerbate intestinal inflammation in a dextran sodium sulfate colitis model using transgenic mice expressing human CD89. Our data thus implicate a link between IgA-coated BEVs and intestinal inflammation via CD89<sup>+</sup> immune cells, and also hint a potential new therapeutic target for UC.

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Publication Details

Journal
Nature Communications
Published
2025-04-29
DOI
https://doi.org/10.1038/s41467-025-59354-5
Citations
12
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
9.67

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article

Enrichment of human IgA-coated bacterial vesicles in ulcerative colitis as a driver of inflammation

Georg Busslinger, Herbert Strobl, Carmen Tam‐Amersdorfer, Leo Eberl et al.
12 citations
Nature Communications
Extracellular vesicles in disease
9.67
article

Enrichment of human IgA-coated bacterial vesicles in ulcerative colitis as a driver of inflammation

Georg Busslinger, Herbert Strobl, Carmen Tam‐Amersdorfer, Leo Eberl, Gregor Gorkiewicz, Christina Passegger, Lukas Binder, Andreas Blesl, Dominik Fleischhacker, Kristina Schild-Prüfert, Stefan Schild, Ellen L. Zechner, Ratchara Kalawong, Christoph Högenauer, Himadri B Thapa, Yi‐Chi Chen, Paul Kohl, Michael R Gerstorfer, Jana Strahlhofer
article en
12 citations

Abstract

The gut microbiome contributes to chronic inflammatory responses in ulcerative colitis (UC), but molecular mechanisms and disease-relevant effectors remain unclear. Here we analyze the pro-inflammatory properties of colonic fluid obtained during colonoscopy from UC and control patients. In patients with UC, we find that the pelletable effector fraction is composed mostly of bacterial extracellular vesicles (BEVs) that exhibit high IgA-levels and incite strong pro-inflammatory responses in IgA receptor-positive (CD89<sup>+</sup>) immune cells. Biopsy analyses reveal higher infiltration of CD89<sup>+</sup> immune cells in the colonic mucosa from patients with UC than control individuals. Further studies show that IgA-coated BEVs, but not host-derived vesicles nor soluble IgA, are potent activators of pro-inflammatory responses in CD89<sup>+</sup> cells. IgA-coated BEVs also exacerbate intestinal inflammation in a dextran sodium sulfate colitis model using transgenic mice expressing human CD89. Our data thus implicate a link between IgA-coated BEVs and intestinal inflammation via CD89<sup>+</sup> immune cells, and also hint a potential new therapeutic target for UC.

Nature CommunicationsVol. 16(1)
Austrian Academy of Sciences (AT), University of Graz (AT), Medical University of Graz (AT), University of Zurich (CH), Graz University of Technology (AT), BioTechMed-Graz (AT), CeMM Research Center for Molecular Medicine (AT), Austrian Agency for Health and Food Safety (AT)
Austrian Science Fund, Karl-Franzens-Universität Graz, Medizinische Universität Graz, BioTechMed-Graz, CSL Limited
Good health and well-being
Openalex Percentile: Top 2%
Extracellular vesicles in disease
9.67
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