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Identification of Chitinase-3-Like Protein 1 as a Novel Neutrophil Antigenic Target in Crohn's Disease

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Autor
Deutschmann C., Sowa M., Murugaiyan J., Roesler U., Röber N., Conrad K., Laass M.W., Bogdanos D., Sipeki N., Papp M., Rödiger S., Roggenbuck D., Schierack P.
Fecha
2019
Language
en
DOI
10.1093/ecco-jcc/jjz012
Materia
chitinase 3 like protein 1
immunoglobulin A
immunoglobulin G
neutrophil cytoplasmic antibody
autoantibody
biological marker
chitinase 3 like protein 1
immunoglobulin
neutrophil cytoplasmic antibody
adolescent
adult
Article
celiac disease
child
cohort analysis
controlled study
Crohn disease
disease course
enzyme linked immunosorbent assay
female
human
human cell
immunoglobulin production
major clinical study
male
matrix assisted laser desorption ionization time of flight mass spectrometry
neutrophil
pathogenesis
prevalence
priority journal
protein analysis
protein isolation
retrospective study
serology
two dimensional electrophoresis
ulcerative colitis
Western blotting
blood
case control study
Crohn disease
Germany
immunology
matrix-assisted laser desorption-ionization mass spectrometry
neutrophil
Adolescent
Adult
Antibodies, Antineutrophil Cytoplasmic
Autoantibodies
Biomarkers
Blotting, Western
Case-Control Studies
Child
Chitinase-3-Like Protein 1
Crohn Disease
Enzyme-Linked Immunosorbent Assay
Female
Germany
Humans
Immunoglobulins
Male
Neutrophils
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Oxford University Press
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Resumen
Background and Aims: There is an increasing incidence of inflammatory bowel disease [IBD]. Autoimmune responses are involved in the pathophysiology of IBD, but their underlying pathways and target antigens have not yet been fully elucidated. Methods: Autoantigenic targets in IBD were identified after separation of whole cell proteins isolated from neutrophils using two-dimensional electrophoresis and matrix assisted laser desorption ionization - time of flight mass spectrometry-based protein identification of the spots that displayed Western blotting signals with anti-neutrophil cytoplasmic antibody-positive sera. The prevalence of IgG, IgA and secretory IgA [sIgA] to chitinase 3-like protein 1 [CHI3L1] was analysed by enzyme-linked immunosorbent assays using recombinant CHI3L1 in 110 patients with Crohn's disease [CD], 95 with ulcerative colitis [UC], 126 with coeliac disease [CeD] and 86 healthy controls [HCs]. Results: The 18-glycosylhydrolase family member CHI3L1 was identified as a neutrophil autoantigenic target. CD patients displayed significantly higher levels of IgG to CHI3L1 than patients with UC and CeD (p < 0.0001, respectively). IgA and sIgA to CHI3L1 was significantly higher in CD than in UC, CeD and HCs [p < 0.0001, respectively]. IgA and sIgA to CHI3L1 demonstrated the highest prevalence in CD [25.5%, 28/110; and 41.8%%, 46/110] compared to HCs [2.3%, 2/86; and 4.7%%, 4/86; p = 0.0015 and p < 0.0001] and are associated with a more complicated progression of CD. Conclusion: CHI3L1 is a novel neutrophil autoantigenic target in CD. IgA and sIgA to CHI3L1 may serve as novel markers for CD and may facilitate the serological diagnosis of IBD. © 2019 European Crohn's and Colitis Organisation (ECCO) 2019.
URI
http://hdl.handle.net/11615/73242
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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