دورية أكاديمية

Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ+ T and B Cells

التفاصيل البيبلوغرافية
العنوان: Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ+ T and B Cells
المؤلفون: Cristina Cifaldi, Maria Chiriaco, Gigliola Di Matteo, Silvia Di Cesare, Scarselli Alessia, Paola De Angelis, Francesca Rea, Giulia Angelino, Maria Pastore, Valentina Ferradini, Daria Pagliara, Caterina Cancrini, Paolo Rossi, Alice Bertaina, Andrea Finocchi
المصدر: Frontiers in Immunology, Vol 8 (2017)
بيانات النشر: Frontiers Media S.A., 2017.
سنة النشر: 2017
المجموعة: LCC:Immunologic diseases. Allergy
مصطلحات موضوعية: novel X-linked inhibitor of apoptosis mutation, very early-onset inflammatory bowel disease, immunodeficiency, hemapoietic stem cells transplant, immune and gastrointestinal recovery, Immunologic diseases. Allergy, RC581-607
الوصف: Monogenic defects in genes related to primary immunodeficiencies can be responsible for inflammatory bowel disease (IBD). Mutations in the X-linked inhibitor of apoptosis (XIAP) gene have been described in several patients suffering from IBD and, in particular, with very early-onset inflammatory bowel disease (VEOIBD) features. We report a VEOIBD child with a novel XIAP gene mutation characterized by a complicated disease course, which is unresponsive to several medical treatment options. A next-generation sequencing was performed and revealed a de novo hemizygous mutation in XIAP gene: c.565T>C p.L189P. After mutation discovery, we investigated the XIAP protein expression and nucleotide-binding oligomerization domain protein 2 (NOD2) signaling by western blotting. Flow-cytometry was used to analyze intracellular protein expression in different cell subsets and T cell apoptosis. We observed reduced protein expression in lymphocytes, granulocytes, monocytes, an Epstein–Barr virus-immortalized B cell line as well as increased apoptosis, and impairment in NOD2 signaling. The child was successfully treated with HLA-haploidentical hemapoietic stem cells transplant, acquired from his mother, after ex vivo elimination of α/β T cells and CD19 B cells. One year after the transplant, we repeated the analysis to appreciate the changes in his impairments. The recovery of XIAP protein expression, function, and normalization of apoptosis were observed. Our report emphasizes the important role of genetic analysis in the diagnosis of VEOIBD, illustrates the complete immunological and gastrointestinal recovery after transplant, and shows one of the few successful transplant cases of XIAP patients.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1664-3224
Relation: http://journal.frontiersin.org/article/10.3389/fimmu.2017.01893/full; https://doaj.org/toc/1664-3224
DOI: 10.3389/fimmu.2017.01893
URL الوصول: https://doaj.org/article/bad1f302d2564a8aa197a76ac5604c75
رقم الأكسشن: edsdoj.bad1f302d2564a8aa197a76ac5604c75
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16643224
DOI:10.3389/fimmu.2017.01893