CX3CL1-CX3CR1 Axis: A New Player in Coeliac Disease Pathogenesis

• Published in: Nutrients 2019-10, Vol.11 (11), p.2551
• Main Authors: Fernández-Prieto, Marta, Fernández-Aceñero, María Jesús, López-Palacios, Natalia, Bodas, Andrés, Farrais, Sergio, Cuevas, David, Pascual, Virginia, Cerón-Nieto, M Ángeles, Horta-Herrera, Saúl, Espino-Paisán, Laura, Salazar, Isabel, Núñez, Concepción
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Celiac disease; Celiac Disease - genetics; Celiac Disease - immunology; Celiac Disease - metabolism; Chemokine CX3CL1 - genetics; Chemokine CX3CL1 - metabolism; Chemokines; coeliac disease; CX3C Chemokine Receptor 1 - genetics; CX3C Chemokine Receptor 1 - metabolism; cx3cl1; cx3cr1; CX3CR1 protein; Cytokines; Diagnosis; Diagnostic systems; Diet; Disease; Enzyme-linked immunosorbent assay; Enzymes; Female; fractalkine; Gastroenterology; Gene expression; Gene Expression Regulation - physiology; Genetic Predisposition to Disease; Gluten; Glutens - immunology; Humans; Hypersensitivity - immunology; Immunoglobulins; Immunohistochemistry; Inflammation; Lymphocytes; Lymphocytes T; Male; Middle Aged; Nutrition; Paraffins; Pediatrics; Proteins; Young Adult; γ-Interferon
• ISSN: 2072-6643; 2072-6643
• DOI: 10.3390/nu11112551

The CX3CL1-CX3CR1 axis has been related to numerous diseases. The aim of our study was to investigate its involvement in coeliac disease (CD) pathogenesis, particularly in the early phase of the disease. We collected peripheral blood from CD patients and controls, enrolled in a 3-day gluten challenge, to study soluble CX3CL1, I-TAC and MIG by Luminex, and gene expression by qPCR, and CX3CR1 protein expression in monocytes and CD8 , CD4 and γδ T cells, by flow cytometry. We also analysed the expression of the and mRNA and protein in the duodenal biopsies of CD patients with active and treated disease, and in non-CD control individuals, by qPCR and immunohistochemistry. After the gluten challenge, increased levels of CX3CL1, I-TAC and MIG proteins were observed in the peripheral blood of CD patients, with no changes in mRNA, or mRNA and protein. Regarding duodenal tissue, CX3CL1 was absent or barely present in the superficial and basal epithelium of CD patients, contrasting with the moderate to high levels present in controls. CX3CL1 seems to be involved in the appearance and progression of CD, and it appears to be a potential diagnostic biomarker. Its use as an alternative therapeutic target in CD deserves further research.