Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Elin Bergseng"'
Autor:
Chu-Young Kim, Elin Bergseng, Mallur S. Madhusudhan, Priya Jayaraman, Ludvig M. Sollid, Thanh Binh Nguyen
Publikováno v:
Journal of Biological Chemistry. 292:9218-9228
Human leukocyte antigen (HLA)-DQ2.5 (DQA1*05/DQB1*02) is a class-II major histocompatibility complex protein associated with both type 1 diabetes and celiac disease. One unusual feature of DQ2.5 is its high class-II-associated invariant chain peptide
Autor:
Rasmus Iversen, Lisa Richter, Rahel Frick, Inger Sandlie, Ludvig M. Sollid, Omri Snir, Shuo-Wang Qiao, Knut E.A. Lundin, Geir Åge Løset, Frode L. Jahnsen, Jeffrey J. Gray, Jørgen Jahnsen, Ole J. B. Landsverk, Jeliazko R. Jeliazkov, Elin Bergseng, Stian Foss, Kristin Støen Gunnarsen, Lene Støkken Høydahl
Background & Aims Development of celiac disease is believed to involve the transglutaminase-dependent response of CD4+ T cells toward deamidated gluten peptides in the intestinal mucosa of individuals with specific HLA-DQ haplotypes. We investigated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5344f7bfe12ca7c42d15336735a78fc9
https://europepmc.org/articles/PMC6441630/
https://europepmc.org/articles/PMC6441630/
Autor:
Knut E.A. Lundin, Ludvig M. Sollid, Shuo-Wang Qiao, Elin Bergseng, Asbjørn Christophersen, Louise Fremgaard Risnes
Publikováno v:
The Journal of Immunology. 196:2819-2826
Celiac disease (CD) is an HLA-associated disorder characterized by a harmful T cell response to dietary gluten. It is not understood why most individuals who carry CD-associated HLA molecules, such as HLA-DQ2.5, do not develop CD despite continuous g
Autor:
Ludvig M. Sollid, Søren Buus, Magnus Ø. Arntzen, Gustavo A. de Souza, Ståle Nygård, Siri Dørum, Morten Nielsen, Elin Bergseng
Publikováno v:
Bergseng, E, Dørum, S, Arntzen, M Ø, Nielsen, M, Nygård, S, Buus, S, de Souza, G A & Sollid, L M 2014, ' Different binding motifs of the celiac disease-associated HLA molecules DQ2.5, DQ2.2, and DQ7.5 revealed by relative quantitative proteomics of endogenous peptide repertoires ', Immunogenetics, vol. 67, no. 2, pp. 73-84 . https://doi.org/10.1007/s00251-014-0819-9
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Immunogenetics
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Immunogenetics
Celiac disease is caused by intolerance to cereal gluten proteins, and HLA-DQ molecules are involved in the disease pathogenesis by presentation of gluten peptides to CD4+ T cells. The α- or β-chain sharing HLA molecules DQ2.5, DQ2.2, and DQ7.5 dis
Autor:
Elin Bergseng, Inger Sandlie, Knut E.A. Lundin, Lene Støkken Høydahl, Louise Fremgaard Risnes, M. Fleur du Pré, Shiva Dahal-Koirala, Ralf Stefan Neumann, Rahel Frick, Geir Åge Løset, Kristin Støen Gunnarsen, Bjørn Dalhus, Shuo-Wang Qiao, Terje Frigstad, Ludvig M. Sollid
Publikováno v:
JCI Insight. 2
Selection of biased T cell receptor (TCR) repertoires across individuals is seen in both infectious diseases and autoimmunity, but the underlying molecular basis leading to these shared repertoires remains unclear. Celiac disease (CD) occurs primaril
Autor:
Knut Ea Lundin, Jørgen Jahnsen, Shuo-Wang Qiao, Asbjørn Christophersen, Elin Bergseng, Melinda Ráki, Ludvig M. Sollid
Publikováno v:
United European Gastroenterology Journal. 2:268-278
Background: Diagnosing coeliac disease (CD) can be challenging, despite highly specific autoantibodies and typical mucosal changes in the small intestine. The T-cell response to gluten is a hallmark of the disease that has been hitherto unexploited i
Autor:
Jørgen Jahnsen, Michael Bodd, Ludvig M. Sollid, Elin Bergseng, Knut E.A. Lundin, Melinda Ráki
Publikováno v:
European Journal of Immunology. 43:2605-2612
Knowledge of the frequency of disease-driving CD4⁺ T cells in lesions of chronic human inflammatory diseases is limited. In celiac disease (CD), intestinal gluten-reactive CD4⁺ T cells, which recognize gluten peptides only in the context of the d
Autor:
Elin Bergseng, Magnus Ø. Arntzen, Siri Dørum, Ludvig M. Sollid, Øyvind Steinsbø, Gustavo A. de Souza
Publikováno v:
Scientific Reports
This study aimed to identify proteolytic fragments of gluten proteins recognized by recombinant IgG1 monoclonal antibodies generated from single IgA plasma cells of celiac disease lesions. Peptides bound by monoclonal antibodies in complex gut-enzyme
Publikováno v:
Human Immunology. 73:376-381
We describe the gluten T-cell response of a DR7DQ2/DR9DQ9 heterozygous celiac disease patient (CD555). Interestingly, this patient had T cells recognizing gluten in the context of human leukocyte antigen (HLA) molecules of both haplotypes. For the DR
Autor:
Chu-Young Kim, Ludvig M. Sollid, Elin Bergseng, Axel Berg-Larsen, Lars Egil Fallang, Kinya Hotta
Publikováno v:
Nature Immunology. 10:1096-1101
Celiac disease driven by an antigluten T cell response is strongly associated with the histocompatibility antigen HLA-DQ2.5 but is barely associated with HLA-DQ2.2. Yet these molecules have very similar peptide-binding motifs and both present gluten