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Autor(en) / Beteiligte
Titel
Subsets of mononuclear phagocytes are enriched in the inflamed colons of patients with IBD
Ist Teil von
  • BMC immunology, 2019-11, Vol.20 (1), p.42-42, Article 42
Ort / Verlag
England: BioMed Central Ltd
Erscheinungsjahr
2019
Link zum Volltext
Quelle
Electronic Journals Library
Beschreibungen/Notizen
  • Myeloid cells, especially mononuclear phagocytes, which include monocytes, macrophages and dendritic cells (DC), play vital roles in innate immunity, and in the initiation and maintenance of adaptive immunity. While T cell-associated activation pathways and cytokines have been identified and evaluated in inflammatory bowel disease (IBD) patients (Neurath, Nat Rev Gastroenterol Hepatol 14:269-78, 1989), the role of mononuclear phagocytes are less understood. Recent reports support the crucial role of DC subsets in the development of acute colitis models (Arimura et al., Mucosal Immunol 10:957-70, 2017), and suggest they may contribute to the pathogenesis of ulcerative colitis (UC) by inducing Th1/Th2/Th17 responses (Matsuno et al., Inflamm Bowel Dis 23:1524-34, 2017). We performed in silico analysis and evaluated the enrichment of immune cells, with a focus on mononuclear phagocytes in IBD patient colonic biopsies. Samples were from different gut locations, with different levels of disease severity, and with treatment response to current therapies. We observe enrichment of monocytes, M1 macrophages, activated DCs (aDCs) and plasmacytoid dendritic cells (pDCs) in inflamed tissues from various gut locations. This enrichment correlates with disease severity. Additionally, the same mononuclear phagocytes subsets are among the top enriched cell types in both infliximab and vedolizumab treatment non-responder samples. We further investigated the enrichment of selected DC and monocyte subsets based on gene signatures derived from a DC- and monocyte-focused single cell RNA-seq (scRNA-seq) study (Villani et al., Science 356:eaah4573, 2017), and verified enrichment in both inflamed tissues and those with treatment resistance. Moreover, we validated an increased mononuclear phagocyte subset abundance in a Dextran Sulphate Sodium (DSS) induced colitis model in C57Bl/6 mice representative of chronic inflammation. We conducted an extensive analysis of immune cell populations in IBD patient colonic samples and identified enriched subsets of monocytes, macrophages and dendritic cells in inflamed tissues. Understanding how they interact with other immune cells and other cells in the colonic microenvironment such as epithelial and stromal cells will help us to delineate disease pathogenesis.
Sprache
Englisch
Identifikatoren
ISSN: 1471-2172
eISSN: 1471-2172
DOI: 10.1186/s12865-019-0322-z
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_ede918ef554f43a5adcaa2e2d508ce3b
Format
Schlagworte
Adaptive immunity, Analysis, Animals, Antibodies, Monoclonal, Humanized - pharmacology, Antibodies, Monoclonal, Humanized - therapeutic use, Antigens, Biopsy, Cell activation, Cellular Microenvironment, Colon, Colon - immunology, Colon - metabolism, Colon - pathology, Crohn’s disease, Cytokines, Cytokines - metabolism, Dendritic cells, Dendritic Cells - immunology, Dendritic Cells - metabolism, Dendritic Cells - pathology, Dextran, Dextrans, Drug Resistance, Endoscopy, Gastrointestinal diseases, Gene expression, Gene Expression Profiling, Genes, Genetic research, Helper cells, House mouse, Humans, Immunophenotyping, Inflammation, Inflammatory bowel disease, Inflammatory bowel diseases, Inflammatory Bowel Diseases - drug therapy, Inflammatory Bowel Diseases - immunology, Inflammatory Bowel Diseases - metabolism, Inflammatory Bowel Diseases - pathology, Infliximab, Infliximab - pharmacology, Infliximab - therapeutic use, Innate immunity, Intestine, Leukocyte Count, Leukocytes (mononuclear), Lymphocytes, Lymphocytes T, Macrophages, Macrophages - immunology, Macrophages - metabolism, Macrophages - pathology, Mice, Microenvironments, Monoclonal antibodies, Monocytes, Monocytes - immunology, Monocytes - metabolism, Monocytes - pathology, Mononuclear Phagocyte System - immunology, Mononuclear Phagocyte System - metabolism, Mononuclear Phagocyte System - pathology, Mononuclear phagocytes, Mucosa, Myeloid cells, Pathogenesis, Patients, Phagocytes, Polysaccharides, RNA, Small intestine, Stromal cells, T cells, T-Lymphocytes - immunology, T-Lymphocytes - metabolism, T-Lymphocytes - pathology, Tumor necrosis factor-α, Ulcerative colitis, Vedolizumab

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