Elin Bergseng

Oslo, Norway

Last Updated: 09/26/2026

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Found 11 publications

Plasma Cells Are the Most Abundant Gluten Peptide MHC-expressing Cells in Inflamed Intestinal Tissues From Patients With Celiac Disease.

Plasma Cells Are the Most Abundant Gluten Peptide MHC-expressing Cells in Inflamed Intestinal Tissues From Patients With Celiac Disease.

Journal: Gastroenterology

Published: December 24, 2017

A TCRα framework-centered codon shapes a biased T cell repertoire through direct MHC and CDR3β interactions.

A TCRα framework-centered codon shapes a biased T cell repertoire through direct MHC and CDR3β interactions.

Journal: JCI insight

Published: May 17, 2017

Unraveling the structural basis for the unusually rich association of human leukocyte antigen DQ2.5 with class-II-associated invariant chain peptides.

Unraveling the structural basis for the unusually rich association of human leukocyte antigen DQ2.5 with class-II-associated invariant chain peptides.

Journal: The Journal of biological chemistry

Published: March 07, 2017

Gluten-specific antibodies of celiac disease gut plasma cells recognize long proteolytic fragments that typically harbor T-cell epitopes.

Gluten-specific antibodies of celiac disease gut plasma cells recognize long proteolytic fragments that typically harbor T-cell epitopes.

Journal: Scientific reports

Published: October 19, 2015

Healthy HLA-DQ2.5+ Subjects Lack Regulatory and Memory T Cells Specific for Immunodominant Gluten Epitopes of Celiac Disease.

Healthy HLA-DQ2.5+ Subjects Lack Regulatory and Memory T Cells Specific for Immunodominant Gluten Epitopes of Celiac Disease.

Journal: Journal of immunology (Baltimore, Md. : 1950)

Published: May 19, 2015

Small bowel, celiac disease and adaptive immunity.

Small bowel, celiac disease and adaptive immunity.

Journal: Digestive diseases (Basel, Switzerland)

Published: May 01, 2015

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.

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.

Journal: Immunogenetics

Published: October 24, 2014

HLA-DQ molecules as affinity matrix for identification of gluten T cell epitopes.

HLA-DQ molecules as affinity matrix for identification of gluten T cell epitopes.

Journal: Journal of immunology (Baltimore, Md. : 1950)

Published: September 28, 2014

Tetramer-visualized gluten-specific CD4+ T cells in blood as a potential diagnostic marker for coeliac disease without oral gluten challenge.

Tetramer-visualized gluten-specific CD4+ T cells in blood as a potential diagnostic marker for coeliac disease without oral gluten challenge.

Journal: United European gastroenterology journal

Published: February 19, 2014

Direct cloning and tetramer staining to measure the frequency of intestinal gluten-reactive T cells in celiac disease.

Direct cloning and tetramer staining to measure the frequency of intestinal gluten-reactive T cells in celiac disease.

Journal: European journal of immunology

Published: January 26, 2013

Evidence that HLA-DQ9 confers risk to celiac disease by presence of DQ9-restricted gluten-specific T cells.

Evidence that HLA-DQ9 confers risk to celiac disease by presence of DQ9-restricted gluten-specific T cells.

Journal: Human immunology

Published: November 02, 2011

Showing 1-11 of 11

Last Updated: 09/26/2026