Specific gut pathobionts escape antibody coating and are enriched during flares in patients with severe Crohn’s disease

Author:

Eriksen CarstenORCID,Danneskiold-Samsøe Niels BanhosORCID,Moll Janne MarieORCID,Myers Pernille NeveORCID,Bondegaard Pi W,Vejrum Simone,Hansen Tine Brodka,Rosholm Lisbeth Buus,Rausch PhilippORCID,Allin Kristine HøjgaardORCID,Jess TineORCID,Kristiansen KarstenORCID,Penders JohnORCID,Jonkers DaisyORCID,Brix SusanneORCID

Abstract

ObjectivePatients with Crohn’s disease (CD) exhibit great heterogeneity in disease presentation and treatment responses, where distinct gut bacteria and immune interactions may play part in the yet unresolved disease aetiology. Given the role of antibodies in the barrier defence against microbes, we hypothesised that gut bacterial antibody-coating patterns may influence underlying disease-mediated processes.DesignAbsolute and relative single and multicoating of gut bacteria with IgA, IgG1, IgG2, IgG3 and IgG4 in patients with CD and healthy controls were characterised and compared with disease activity. IgG2-coated and non-coated taxa from patients with severe CD were identified, profiled for pathogenic characteristics and monitored for enrichment during active disease across cohorts.ResultsPatients with severe CD exhibited higher gut bacterial IgG2-coating. Supervised clustering identified 25 bacteria to be enriched in CD patients with high IgG2-coating. Sorting, sequencing andin silico-based assessments of the virulent potential of IgG2-coated and bulk stool bacteria were performed to evaluate the nature and pathogenicity of IgG2-coated and non-coated bacteria. The analyses demonstrated IgG2-coating of both known pathogenic and non-pathogenic bacteria that co-occurred with two non-coated pathobionts,CampylobacterandMannheimia. The two non-coated pathobionts exhibited low prevalence, rarely coincided and were strongly enriched during disease flares in patients with CD across independent and geographically distant cohorts.ConclusionDistinct gut bacterial IgG2-coating was demonstrated in patients with severe CD and during disease flares. Co-occurrence of non-coated pathobionts with IgG2-coated bacteria points to an uncontrolled inflammatory condition in severe CD mediated via escape from antibody coating by two gut pathobionts.

Funder

Technical University of Denmark

Danish National Research Foundation

Publisher

BMJ

Subject

Gastroenterology

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