Search Results - "Hörnquist, E"
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Altered faecal and mucosal microbial composition in post‐infectious irritable bowel syndrome patients correlates with mucosal lymphocyte phenotypes and psychological distress
Published in Alimentary pharmacology & therapeutics (01-02-2015)“…Summary Background A subset of irritable bowel syndrome (IBS) patients, denoted post‐infectious IBS (PI‐IBS), develop symptoms after an enteric infection…”
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Rapid migration of thymic emigrants to the colonic mucosa in ulcerative colitis patients
Published in Clinical and experimental immunology (01-11-2010)“…Inflammatory bowel disease (IBD) is associated with imbalances of the local intestinal immune responses, with dysregulated CD4⁺ T cells contributing to the…”
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Pathogenesis of Microscopic Colitis: A Systematic Review
Published in Journal of Crohn's and colitis (2022)“…Abstract Background Whereas the exact aetiology of microscopic colitis [MC] remains unknown, a dysregulated immune response to luminal factors or medications…”
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PP112-SUN ALTERED COMPOSITION OF LYMPHOCYTES IN THE INTESTINAL MUCOSA OF PI-IBS PATIENTS
Published in Clinical nutrition (Edinburgh, Scotland) (01-09-2013)Get full text
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Dextran Sulfate Sodium-induced Colitis Generates a Transient Thymic Involution - Impact on Thymocyte Subsets
Published in Scandinavian journal of immunology (01-05-2007)“…One of the most widely used animal models for inflammatory bowel disease (IBD) is the dextran sulfate sodium (DSS)-induced colitis. We have previously reported…”
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Regression of Peyer's patches in Gαi2 deficient mice prior to colitis is associated with reduced expression of Bcl-2 and increased apoptosis
Published in Gut (01-09-2002)“…Background: G protein deficient (Gαi2−/−) mice spontaneously develop an inflammatory bowel disease (IBD) closely resembling ulcerative colitis. Previous…”
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Toll‐like Receptor Cross‐hyporesponsiveness is Functional in Interleukin‐1‐receptor‐associated Kinase‐1 (IRAK‐1)‐deficient Macrophages: Differential Role Played by IRAK‐1 in Regulation of Tumour Necrosis Factor and Interleukin‐10 Production
Published in Scandinavian journal of immunology (01-05-2008)“…Signalling downstream Toll‐like receptors (TLR) is regulated at several levels in order to activate the immune response and prevent excessive inflammation…”
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Acellular Bordetella pertussis vaccine enhances mucosal interleukin‐10 production, induces apoptosis of activated Th1 cells and attenuates colitis in Gαi2‐deficient mice
Published in Clinical and experimental immunology (01-07-2005)“…Summary Mice deficient for the inhibitory G protein subunit α2 (Gαi2–/–) spontaneously develop a progressive inflammatory bowel disease resembling ulcerative…”
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Decreased leptin production in mice after onset of ulcerative colitis-like disease
Published in Scandinavian journal of gastroenterology (01-11-2004)Get full text
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Acellular Bordetella pertussis vaccine enhances mucosal interleukin-10 production, induces apoptosis of activated Th1 cells and attenuates colitis in Galphai2-deficient mice
Published in Clinical and experimental immunology (01-07-2005)“…Mice deficient for the inhibitory G protein subunit alpha2 (Galphai2(-/-)) spontaneously develop a progressive inflammatory bowel disease resembling ulcerative…”
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CD8‐deficient mice exhibit augmented mucosal immune responses and intact adjuvant effects to cholera toxin
Published in Immunology (01-02-1996)“…We used normal, CD4 and CD8 gene‐targeted mice to investigate the role of CD4+ and CD8+ T cells in the regulation of gut mucosal immune responses following…”
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Paradoxical IgA immunity in CD4-deficient mice. Lack of cholera toxin- specific protective immunity despite normal gut mucosal IgA differentiation
Published in The Journal of immunology (1950) (15-09-1995)“…Using normal and CD4 gene-targeted (CD4-/-) mice, we asked whether mucosal immune responses and IgA B cell differentiation require the presence of CD4+ T…”
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Interaction of Bordetella pertussis with mast cells, modulation of cytokine secretion by pertussis toxin
Published in Cellular microbiology (01-03-2001)“…Together with macrophages and dendritic cells, mast cells have recently been shown to interact with certain pathogenic bacteria and present microbial antigens…”
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Serum interleukin-1 receptor antagonist is an early indicator of colitis onset in Gαi2-deficient mice
Published in World journal of gastroenterology : WJG (28-01-2006)“…AIM: To study the serum concentration of IL-1β, IL-1 receptor antagonist (IL-1Ra) and IL-18 in Gαi2-deficient mice at the age of 6 (healthy), 12 (pre-colitic)…”
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Diagnosis and management of microscopic colitis: current perspectives
Published in Clinical and experimental gastroenterology (01-01-2014)“…Collagenous colitis and lymphocytic colitis, together constituting microscopic colitis, are common causes of chronic diarrhea. They are characterized…”
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Cholera toxin adjuvant greatly promotes antigen priming of T cells
Published in European journal of immunology (01-09-1993)“…Cholera toxin (CT) given perorally is a powerful mucosal immunogen and adjuvant. Information that explains the adjuvant effect of CT may be used for the…”
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Antibody response to dietary and autoantigens in Gαi2-deficient mice
Published in European journal of gastroenterology & hepatology (01-12-2001)“…BACKGROUND Mice with a targeted mutation in the G protein subunit Gαi2 gene develop a colonic mucosal inflammation, with a highly activated B-cell response. We…”
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Lack of Local Suppression in Orally Tolerant CD8-Deficient Mice Reveals a Critical Regulatory Role of CD8+ T Cells in the Normal Gut Mucosa
Published in The Journal of immunology (1950) (15-01-1998)“…We found that feeding keyhole limpet hemocyanin (KLH) to CD8-deficient (CD8-/-) mice induced oral tolerance that was comparable in both magnitude and quality…”
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The mucosal adjuvant effects of cholera toxin and immune‐stimulating complexes differ in their requirement for IL‐12, indicating different pathways of action
Published in European journal of immunology (01-06-1999)“…Adjuvants that can improve mucosal vaccine efficacy are much warranted. In this comparative study between cholera toxin (CT) and immune‐stimulating complexes…”
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