Articles producció científica> Medicina i Cirurgia

Similar Responses of Intestinal T Cells From Untreated Children and Adults With Celiac Disease to Deamidated Gluten Epitopes

  • Identification data

    Identifier: imarina:6389234
    Authors:
    Ráki MDahal-Koirala SYu HKorponay-Szabó IGyimesi JCastillejo GJahnsen JQiao SSollid L
    Abstract:
    © 2017 AGA Institute Background & Aims Celiac disease is a chronic small intestinal inflammatory disorder mediated by an immune response to gluten peptides in genetically susceptible individuals. Celiac disease is often diagnosed in early childhood, but some patients receive a diagnosis late in life. It is uncertain whether pediatric celiac disease is distinct from adult celiac disease. It has been proposed that gluten-reactive T cells in children recognize deamidated and native gluten epitopes, whereas T cells from adults only recognize deamidated gluten peptides. We studied the repertoire of gluten epitopes recognized by T cells from children and adults. Methods We examined T-cell responses against gluten by generating T-cell lines and T-cell clones from intestinal biopsies of adults and children and tested proliferative response to various gluten peptides. We analyzed T cells from 14 children (2−5 years old) at high risk for celiac disease who were followed for celiac disease development. We also analyzed T cells from 6 adults (26−55 years old) with untreated celiac disease. All children and adults were positive for HLA-DQ2.5. Biopsies were incubated with gluten digested with chymotrypsin (modified or unmodified by the enzyme transglutaminase 2) or the peptic-tryptic digest of gliadin (in native and deamidated forms) before T-cell collection. Results Levels of T-cell responses were higher to deamidated gluten than to native gluten in children and adults. T cells from children and adults each reacted to multiple gluten epitopes. Several T-cell clones were cross-reactive, especially clones that recognized epitopes from γ-and ω-gliadin. About half of the generated T-cell clones from children and adults reacted to unknown epitopes. Conclusions T-cell responses to differe
  • Others:

    Author, as appears in the article.: Ráki M; Dahal-Koirala S; Yu H; Korponay-Szabó I; Gyimesi J; Castillejo G; Jahnsen J; Qiao S; Sollid L
    Department: Medicina i Cirurgia
    URV's Author/s: Castillejo De Villasante, Gemma
    Keywords: Tg2 Preventcd study Cd4 t cell + Autoimmunity preventcd study cd4(+) t cell autoimmunity
    Abstract: © 2017 AGA Institute Background & Aims Celiac disease is a chronic small intestinal inflammatory disorder mediated by an immune response to gluten peptides in genetically susceptible individuals. Celiac disease is often diagnosed in early childhood, but some patients receive a diagnosis late in life. It is uncertain whether pediatric celiac disease is distinct from adult celiac disease. It has been proposed that gluten-reactive T cells in children recognize deamidated and native gluten epitopes, whereas T cells from adults only recognize deamidated gluten peptides. We studied the repertoire of gluten epitopes recognized by T cells from children and adults. Methods We examined T-cell responses against gluten by generating T-cell lines and T-cell clones from intestinal biopsies of adults and children and tested proliferative response to various gluten peptides. We analyzed T cells from 14 children (2−5 years old) at high risk for celiac disease who were followed for celiac disease development. We also analyzed T cells from 6 adults (26−55 years old) with untreated celiac disease. All children and adults were positive for HLA-DQ2.5. Biopsies were incubated with gluten digested with chymotrypsin (modified or unmodified by the enzyme transglutaminase 2) or the peptic-tryptic digest of gliadin (in native and deamidated forms) before T-cell collection. Results Levels of T-cell responses were higher to deamidated gluten than to native gluten in children and adults. T cells from children and adults each reacted to multiple gluten epitopes. Several T-cell clones were cross-reactive, especially clones that recognized epitopes from γ-and ω-gliadin. About half of the generated T-cell clones from children and adults reacted to unknown epitopes. Conclusions T-cell responses to different gluten peptides appear to be similar between adults and children at the time of diagnosis of celiac disease.
    Thematic Areas: Saúde coletiva Nutrição Medicina veterinaria Medicina iii Medicina ii Medicina i Matemática / probabilidade e estatística Interdisciplinar Hepatology General medicine Gastroenterology & hepatology Gastroenterology Educação física Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Biotecnología
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 00165085
    Author's mail: gemma.castillejo@urv.cat
    Record's date: 2024-09-07
    Papper version: info:eu-repo/semantics/acceptedVersion
    Link to the original source: https://www.gastrojournal.org/article/S0016-5085(17)35625-1/fulltext?referrer=https%3A%2F%2Firis.urv.cat%2F#%20
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Papper original source: Gastroenterology. 153 (3): 787-798.e4
    APA: Ráki M; Dahal-Koirala S; Yu H; Korponay-Szabó I; Gyimesi J; Castillejo G; Jahnsen J; Qiao S; Sollid L (2017). Similar Responses of Intestinal T Cells From Untreated Children and Adults With Celiac Disease to Deamidated Gluten Epitopes. Gastroenterology, 153(3), 787-798.e4. DOI: 10.1053/j.gastro.2017.05.016
    Article's DOI: 10.1053/j.gastro.2017.05.016
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2017
    Publication Type: Journal Publications
  • Keywords:

    Gastroenterology,Gastroenterology & Hepatology,Hepatology
    Tg2
    Preventcd study
    Cd4 t cell +
    Autoimmunity
    preventcd study
    cd4(+) t cell
    autoimmunity
    Saúde coletiva
    Nutrição
    Medicina veterinaria
    Medicina iii
    Medicina ii
    Medicina i
    Matemática / probabilidade e estatística
    Interdisciplinar
    Hepatology
    General medicine
    Gastroenterology & hepatology
    Gastroenterology
    Educação física
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Biotecnología
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