Please use this identifier to cite or link to this item: https://hdl.handle.net/1822/58047

TitleCytotoxic T lymphocyte antigen-4 gene polymorphisms and susceptibility to type 1 autoimmune hepatitis in the Tunisian population
Author(s)Chaouali, Marwa
Carvalho, Agostinho
Tezeghdenti, Aymen
Ben Azaiez, Mouna
Cunha, Cristina
Ghazouani, Ezzeddine
Kochkar, Radhia
KeywordsAutoimmune hepatitis
CTLA4 gene polymorphisms
Cytotoxic T-lymphocyte antigen 4
Issue dateSep-2018
PublisherElsevier
JournalGenes and Diseases
CitationChaouali, M., Carvalho, A., Tezeghdenti, A., Azaiez, M. B., Cunha, C., Ghazouani, E., & Kochkar, R. (2018). Cytotoxic T lymphocyte antigen-4 gene polymorphisms and susceptibility to type 1 autoimmune hepatitis in the Tunisian population. Genes & diseases, 5(3), 256-262
Abstract(s)Genetic factors and gene polymorphisms leading to the onset of autoimmune response in autoimmune hepatitis (AIH) are still not full elucidated. Since the CTLA-4 molecule is a key modulator of the lymphocytes responses we hypothezied that deficiencies or mutations in the gene encoding CTLA4 protein may be involved in AIH susceptibility and trigger the autoimmune response. We investigated 3 distinct polymorphic sites (+49A > G, CT60 G > A and -318C > T) of the CTLA4 gene in 50 AIH patients and 100 healthy controls using the KASP genotyping technology. A significant positive association with AIH susceptibility was found for the GG genotype in +49 position of the CTLA4 gene which was significantly higher in AIH patients compared to controls (28% vs 9%, p = 0.003, OR = 3.93 [1.56-9.88]). The CTLA4 A/A genotype in position CT60 was more significantly frequent in controls comparing to AIH patients and could be considered as a protective genotype for the tunisian patients. CTLA4 genotyping in position -318 did not show any statistically significant difference in genotype or allele distribution. The CTLA4 gene polymorphism in position +49 is associated to AIH susceptibility in the Tunisian population. Mutation in the CTLA4 gene may lead to a modification of the CTLA4 protein structure that could have functional relevance in AIH pathogenesis and onset.
TypeArticle
URIhttps://hdl.handle.net/1822/58047
DOI10.1016/j.gendis.2017.12.006
ISSN2352-3042
e-ISSN2352-3042
Publisher versionhttps://www.sciencedirect.com/science/article/pii/S2352304217301034
Peer-Reviewedyes
AccessRestricted access (UMinho)
Appears in Collections:ICVS - Artigos em revistas internacionais / Papers in international journals


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