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Loss of IDO1 Expression From Human Pancreatic ß-Cells Precedes Their Destruction During the Development of Type 1 Diabetes.
Anquetil, Florence; Mondanelli, Giada; Gonzalez, Nathaly; Rodriguez Calvo, Teresa; Zapardiel Gonzalo, Jose; Krogvold, Lars; Dahl-Jørgensen, Knut; Van den Eynde, Benoit; Orabona, Ciriana; Grohmann, Ursula; von Herrath, Matthias G.
Afiliación
  • Anquetil F; La Jolla Institute for Allergy and Immunology, La Jolla, CA.
  • Mondanelli G; University of Perugia, Perugia, Italy.
  • Gonzalez N; La Jolla Institute for Allergy and Immunology, La Jolla, CA.
  • Rodriguez Calvo T; La Jolla Institute for Allergy and Immunology, La Jolla, CA.
  • Zapardiel Gonzalo J; La Jolla Institute for Allergy and Immunology, La Jolla, CA.
  • Krogvold L; Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
  • Dahl-Jørgensen K; Faculty of Dentistry, University of Oslo, Oslo, Norway.
  • Van den Eynde B; Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
  • Orabona C; de Duve Institute, Brussels, Belgium.
  • Grohmann U; Ludwig Institute for Cancer Research, Brussels, Belgium.
  • von Herrath MG; University of Perugia, Perugia, Italy.
Diabetes ; 67(9): 1858-1866, 2018 09.
Article en En | MEDLINE | ID: mdl-29945890
Indoleamine 2,3 dioxygenase-1 (IDO1) is a powerful immunoregulatory enzyme that is deficient in patients with type 1 diabetes (T1D). In this study, we present the first systematic evaluation of IDO1 expression and localization in human pancreatic tissue. Although IDO1 was constitutively expressed in ß-cells from donors without diabetes, less IDO1 was expressed in insulin-containing islets from double autoantibody-positive donors and patients with recent-onset T1D, although it was virtually absent in insulin-deficient islets from donors with T1D. Scatter plot analysis suggested that IDO1 decay occurred in individuals with multiple autoantibodies, prior to ß-cell demise. IDO1 impairment might therefore contribute to ß-cell demise and could potentially emerge as a promising therapeutic target.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estado Prediabético / Enfermedades Autoinmunes / Autoinmunidad / Regulación hacia Abajo / Diabetes Mellitus Tipo 1 / Células Secretoras de Insulina / Indolamina-Pirrol 2,3,-Dioxigenasa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Idioma: En Revista: Diabetes Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estado Prediabético / Enfermedades Autoinmunes / Autoinmunidad / Regulación hacia Abajo / Diabetes Mellitus Tipo 1 / Células Secretoras de Insulina / Indolamina-Pirrol 2,3,-Dioxigenasa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Idioma: En Revista: Diabetes Año: 2018 Tipo del documento: Article