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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd">
<ArticleSet>
	<Article>
		<Journal>
			<PublisherName/>
			<JournalTitle>IJOTM</JournalTitle>
			<Issn>2008-6490</Issn>
			<Volume>8</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="epublish">
				<Year>2017</Year>
				<Month>01</Month>
				<Day>11</Day>
			</PubDate>
		</Journal>
		<ArticleTitle>Interleukin-28B rs12979860 C/T Polymorphism and Acute Cellular Rejection after Liver Transplantation</ArticleTitle>
		<FirstPage>28</FirstPage>
		<LastPage>33</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>H</FirstName>
				<LastName>Fereidooni</LastName>
			</Author>
			<Author>
				<FirstName>N</FirstName>
				<LastName>Azarpira</LastName>
				<Affiliation>Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. negarazarpira@yahoo.com</Affiliation>
			</Author>
			<Author>
				<FirstName>R</FirstName>
				<LastName>Yaghobi</LastName>
			</Author>
			<Author>
				<FirstName>A</FirstName>
				<LastName>Vahdati</LastName>
			</Author>
			<Author>
				<FirstName>SA</FirstName>
				<LastName>Malek-Hosseini</LastName>
			</Author>
		</AuthorList>
		<History>
			<PubDate PubStatus="received">
				<Year>2015</Year>
				<Month>04</Month>
				<Day>07</Day>
			</PubDate>
		</History>
		<Abstract>Background: Interleukin-28 (IL-28B) rs12979860 C/T polymorphism is a known predictor of sustained virological response after antiviral treatment in hepatitis C. IL-28B affects the innate immune system as well as intrahepatic expression level of interferon-stimulated genes.Objective: To investigate the effect of recipient IL-28B polymorphism on occurrence of acute rejection after liver transplantation.Methods: 140 liver allograft recipients were selected. Acute rejection episodes were recorded in 39 patients (AR group); the remaining had normal graft function (non-AR group). 70 normal subjects were also studied as the control group. The IL-28B rs12979860 was genotyped through PCR-RFLP method.Results: No significant difference was found between AR and non-AR groups in terms of genotype and allele frequency. However, the CC genotype was significantly (p&amp;lt;0.001) more frequent in patients than in the control group; the C allele variants increased the risk of end-stage liver disease (OR: 2.60).Conclusion: Liver damage in association with the carriage of IL-28B C allele is associated with a higher likelihood of developing cirrhosis.</Abstract>
	</Article>
</ArticleSet>
