دورية أكاديمية

CIITA promoter polymorphism impairs monocytes HLA-DR expression in patients with septic shock

التفاصيل البيبلوغرافية
العنوان: CIITA promoter polymorphism impairs monocytes HLA-DR expression in patients with septic shock
المؤلفون: Jordi Miatello, Anne-Claire Lukaszewicz, Michael J. Carter, Valérie Faivre, Stéphane Hua, Kim Z. Martinet, Christine Bourgeois, Lluis Quintana-Murci, Didier Payen, Michele Boniotto, Pierre Tissières
المصدر: iScience, Vol 25, Iss 11, Pp 105291- (2022)
بيانات النشر: Elsevier, 2022.
سنة النشر: 2022
المجموعة: LCC:Science
مصطلحات موضوعية: Health sciences, Genetics, Immunology, Science
الوصف: Summary: Low monocyte (m)HLA-DR expression is associated with mortality in sepsis. G-286A∗rs3087456 polymorphism in promoter III of HLA class II transactivator (CIITA), the master regulator of HLA, has been associated with autoimmune diseases but its role in sepsis has never been demonstrated. In 203 patients in septic shock, GG genotype was associated with 28-day mortality and mHLA-DR remained low whereas it increased in patients with AA or AG genotype. In ex vivo cells, mHLA-DR failed to augment in GG in comparison with AG or AA genotype on exposure to IFN-γ. Promoter III transcript levels were similar in control monocytes regardless of genotype and exposure to IFN-γ. Promoter III activity was decreased in GG genotype in monocyte cell line but restored after stimulation with IFN-γ. Hereby, we demonstrated that G-286A∗rs3087456 significantly impact mHLA-DR expression in patients with septic shock in part through CIITA promoter III activity, that can be rescued using IFN-γ.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2589-0042
العلاقة: http://www.sciencedirect.com/science/article/pii/S2589004222015632Test; https://doaj.org/toc/2589-0042Test
DOI: 10.1016/j.isci.2022.105291
الوصول الحر: https://doaj.org/article/92da6f9a85384104a27ad847fa3008d9Test
رقم الانضمام: edsdoj.92da6f9a85384104a27ad847fa3008d9
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:25890042
DOI:10.1016/j.isci.2022.105291