Abstract |
A hallmark of celiac disease is the gluten-dependent production of antibodies specific for deamidated gluten peptides (DGP) and the enzyme transglutaminase 2 (TG2). Both types of antibodies are believed to result from B cells receiving help from gluten-specific CD4+ T cells and differentiating into antibody-producing plasma cells. We have here studied the collaboration between DGP- and TG2-specific B cells with gluten-specific CD4+ T cells using transgenic mice expressing celiac patient-derived T-cell and B-cell receptors, as well as between B-cell transfectants and patient-derived gluten-specific T-cell clones. We show that multivalent TG2-gluten complexes are efficient antigens for both TG2-specific and DGP-specific B cells and allow both types of B cells to receive help from gluten-specific T cells of many different specificities.
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Authors | Christian B Lindstad, Alisa E Dewan, Jorunn Stamnaes, Ludvig M Sollid, M Fleur du Pré |
Journal | PloS one
(PLoS One)
Vol. 16
Issue 11
Pg. e0259082
( 2021)
ISSN: 1932-6203 [Electronic] United States |
PMID | 34731200
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Receptors, Antigen, B-Cell
- Glutens
- Gliadin
- Protein Glutamine gamma Glutamyltransferase 2
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Topics |
- Animals
- B-Lymphocytes
(immunology, metabolism, pathology)
- CD4-Positive T-Lymphocytes
(immunology, metabolism)
- Celiac Disease
(genetics, immunology, pathology)
- Gliadin
(genetics, immunology)
- Glutens
(genetics, immunology)
- Humans
- Mice
- Mice, Transgenic
- Protein Glutamine gamma Glutamyltransferase 2
(genetics, immunology)
- Receptors, Antigen, B-Cell
(genetics)
- T-Lymphocytes
(immunology, metabolism, pathology)
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