Bronchiolitis obliterans after allogeneic hematopoietic stem cell transplantation: The effect of NOD2/CARD15 mutations in a Tunisian population

التفاصيل البيبلوغرافية
العنوان: Bronchiolitis obliterans after allogeneic hematopoietic stem cell transplantation: The effect of NOD2/CARD15 mutations in a Tunisian population
المؤلفون: Mouna Touihri, Manel Chabaane, Slama Hmida, Tarek Ben Othman, Lamia Torjeman, H. Kaabi
المصدر: Human immunology. 80(3)
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Male, Tunisia, Genotype, medicine.medical_treatment, Immunology, Nod2 Signaling Adaptor Protein, Bronchiolitis obliterans, Single-nucleotide polymorphism, Hematopoietic stem cell transplantation, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Risk Factors, NOD2, Immunology and Allergy, Medicine, Humans, Transplantation, Homologous, Bronchiolitis Obliterans, Lung, business.industry, Incidence, Hematopoietic Stem Cell Transplantation, General Medicine, medicine.disease, digestive system diseases, Respiratory Function Tests, Transplantation, 030104 developmental biology, medicine.anatomical_structure, Case-Control Studies, Mutation, Female, Disease Susceptibility, Stem cell, Complication, business, 030215 immunology
الوصف: Bronchiolitis obliterans (BO) is a serious lung complication that can develop after allogenic stem cell transplantation. It has been suggested that single nucleotide polymorphisms (SNPs) that affect the NOD2/CARD15 gene impair its function and result in an uncontrolled innate immune response in the recipient, thereby leading to BO. One hundred eighty-one donor-recipient pairs were analyzed for the association between NOD2 gene variants (SNP8 [Arg702Trp], SNP12 [Gly908Arg], and SNP13 [Leu1007fsinsC]) and the occurrence of BO. Ten patients (2.8%) developed this complication. The incidence of BO increases in recipient variant patient group from 4.7% to 23% in donor Wild-type group in SNP8 (p 0.001). The incidence rose to 19% when the recipient carried the SNP12 variant (p 0.001) in the Tunisian population. Analyses demonstrated that recipient NOD2CARD15 variants (SNP8 and SNP12) present a greater risk in developing BO than recipients without mutation. Our study demonstrated that NOD2/CARD15 typing may be useful in identifying patients at high risk for BO.
تدمد: 1879-1166
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e1659c1d4ac0e2ac8d205a6d2e6f042
https://pubmed.ncbi.nlm.nih.gov/30552907
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....1e1659c1d4ac0e2ac8d205a6d2e6f042
قاعدة البيانات: OpenAIRE