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Il4 Gene Polymorphisms in Iranian Patients With Autoimmune Hepatitis Publisher Pubmed



Yousefi A1 ; Mahmoudi E2 ; Zare Bidoki A3, 6 ; Najmi Varzaneh F2, 4 ; Baradaran Noveiry B2, 4 ; Sadr M2 ; Motamed F1 ; Najafi M1 ; Farahmand F1 ; Rezaei N2, 4, 5
Authors
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Authors Affiliations
  1. 1. Department of Gastroenterology, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Molecular Immunology Research Center, Department of Immunology, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Thrombosis Hemostasis Research Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran
  5. 5. Research Center for Immunodeficiencies, Childrens Medical Center, Tehran University of Medical Sciences, Keshavarz Blvd, Tehran, 14194, Iran
  6. 6. Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran

Source: Expert Review of Gastroenterology and Hepatology Published:2016


Abstract

Background: Autoimmune hepatitis (AIH) is a chronic long-lasting hepatocellular inflammation associated with circulating auto antibodies. In addition to the genetic component, several cytokines have been implicated to be involved in AIH. This study was performed to investigate potential associations of AIH with IL4 gene variants.Method: The studied alleles and genotypes included: IL4G/T allele polymorphisms at position-1098 and C/T allele polymorphisms at two positions (-33 and-590) on the IL4 gene, in addition to the A/G allele polymorphisms at position +1902 on the IL4RA gene.Result: The IL4 C allele and CC genotype at position-590 and TT genotype at position-33 had a significantly higher frequency in AIH patients.Conclusion: This study identified the IL4 C allele and CC genotype susceptibility gene in AIH, which will provide better insights into the mechanisms of AIH and potential therapeutic interventions. © 2016 Informa UK Limited.