Mucosal Plasma Cell Activation and Proximity to Nerve Fibres Are Associated with Glycocalyx Reduction in Diarrhoea-Predominant Irritable Bowel Syndrome: Jejunal Barrier Alterations Underlying Clinical Manifestations

Cristina Pardo‐Camacho(Universitat Autònoma de Barcelona), John‐Peter Ganda Mall(Linköping University), Cristina Martínez(Instituto de Investigación Biomédica de Lleida), Marc Pigrau(Universitat Autònoma de Barcelona), Elba Expósito(Vall d'Hebron Institut de Recerca), Mercé Albert-Bayo(Vall d'Hebron Institut de Recerca), Elisa Melón-Ardanaz(Vall d'Hebron Institut de Recerca), Adoración Nieto(Vall d'Hebron Institut de Recerca), Bruno K. Rodiño‐Janeiro(Vall d'Hebron Institut de Recerca), Marina Fortea(Vall d'Hebron Institut de Recerca), Danila Guagnozzi(Vall d'Hebron Institut de Recerca), Amanda Rodríguez‐Urrutia(Universitat Autònoma de Barcelona), Inés de Torres(Universitat Autònoma de Barcelona), Ignacio Santos-Briones(Universitat Ramon Llull), Fernando Azpiroz(Instituto de Salud Carlos III), Beatriz Lobo(Universitat Autònoma de Barcelona), Carmen Alonso(Universitat Autònoma de Barcelona), Javier Santos(Universitat Autònoma de Barcelona), Ana María González-Castro(Vall d'Hebron Institut de Recerca), María Vicario(Vall d'Hebron Institut de Recerca)
Cells
June 28, 2022
Cited by 16Open Access
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Abstract

Irritable bowel syndrome (IBS) is a disorder of brain-gut interaction characterised by abdominal pain and changes in bowel habits. In the diarrhoea subtype (IBS-D), altered epithelial barrier and mucosal immune activation are associated with clinical manifestations. We aimed to further evaluate plasma cells and epithelial integrity to gain understanding of IBS-D pathophysiology. One mucosal jejunal biopsy and one stool sample were obtained from healthy controls and IBS-D patients. Gastrointestinal symptoms, stress, and depression scores were recorded. In the jejunal mucosa, RNAseq and gene set enrichment analyses were performed. A morphometric analysis by electron microscopy quantified plasma cell activation and proximity to enteric nerves and glycocalyx thickness. Immunoglobulins concentration was assessed in the stool. IBS-D patients showed differential expression of humoral pathways compared to controls. Activation and proximity of plasma cells to nerves and IgG concentration were also higher in IBS-D. Glycocalyx thickness was lower in IBS-D compared to controls, and this reduction correlated with plasma cell activation, proximity to nerves, and clinical symptoms. These results support humoral activity and loss of epithelial integrity as important contributors to gut dysfunction and clinical manifestations in IBS-D. Additional studies are needed to identify the triggers of these alterations to better define IBS-D pathophysiology.


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