﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Hamadan University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Research in Health Sciences</JournalTitle>
      <Issn>2228-7795</Issn>
      <Volume>14</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2014</Year>
        <Month>06</Month>
        <DAY>06</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Evaluation of IFN-Î³ Polymorphism in Visceral Leishmaniasis</ArticleTitle>
    <FirstPage>136</FirstPage>
    <LastPage>139</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Amir Hossein</FirstName>
        <LastName>Maghsood</LastName>
      </Author>
      <Author>
        <FirstName>Golamreza</FirstName>
        <LastName>Jadideslam</LastName>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Fallah</LastName>
      </Author>
      <Author>
        <FirstName>Ahad</FirstName>
        <LastName>Bazmani</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2013</Year>
        <Month>08</Month>
        <Day>24</Day>
      </PubDate>
    </History>
    <Abstract>Background: Leishmaniasis is a tropical disease that is endemic in some areas of Iran, including East Azerbaijan. IFN-Î³ is one of the cytokines that triggers cell-mediated immunity, thus initiating elimination of the infection. This case-control study was performed to investigate the association between the polymorphism of the IFN-Î³ gene at the +874A/T locus and visceral leishmaniasis (VL). Methods: In this study conducted during 2012-2013, 267 participants were selected from individuals living in an endemic area of VL. Subjects were divided into three groups; 86 patients with VL, 82 seropositive individuals without any history of leishmaniasis, and 99 seronegative healthy controls. Genotyping of the IFN-Î³ +874A/T polymorphism was carried out using an Amplification Refractory Mutation System-PCR (ARMS-PCR). Results: The frequency of the +874A allele in the patient group (75.5%) was higher than in the seropositive individuals (54%). The highest frequency of the +874T/T genotype was observed in seropositive individuals, while the patient group had the lowest frequency (34.1% vs. 24.5%). However, these differences were not significant. Conclusion: There was no significant association between IFN-Î³ +874A/T polymorphism and VL.</Abstract>
  </Article>
</ArticleSet>