Lack of association between CTLA-4 and PDCD1 polymorphisms and acute rejection in German liver transplant recipients

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Lack of association between CTLA-4 and PDCD1 polymorphisms and acute rejection in German liver transplant recipients. / Thude, Hansjörg; Schipler, Anna Dorothea; Treszl, Andras; Peine, Sven; Koch, Martina; Sterneck, Martina; Nashan, Björn.

in: HUM IMMUNOL, Jahrgang 74, Nr. 8, 01.08.2013, S. 1041-5.

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@article{76d4495a37b649f6bd0f54fe27189649,
title = "Lack of association between CTLA-4 and PDCD1 polymorphisms and acute rejection in German liver transplant recipients",
abstract = "Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and programmed cell-death 1 (PDCD1) are two genes encoding coinhibitory immunoreceptors that are involved in regulation transplant rejection and tolerance induction. Thus, CTLA-4 and PDCD1 may be good candidate genes to evaluate in liver transplant rejection. In this retrospective study, we investigated whether four functional single nucleotide polymorphisms (SNP) of the CTLA-4 gene and PDCD1 gene were associated with susceptibility to liver transplant rejection. The SNPs -1772T>C (rs733618), -1661A>G (rs4553808) of the CTLA-4 gene, and the SNPs 7146G>A (rs11568821), 7209C>T (rs41386349) of the PDCD1 gene were genotyped by polymerase chain reaction allele specific restriction enzyme analysis (PCR-ASRA) in 100 liver recipients with acute rejection, 104 liver transplant recipients without acute rejection and 100 healthy control individuals. For the selected SNPs we did not detect any significant difference in genotypic and allelic frequencies between liver transplant recipients with and without acute rejection. In conclusion, our results suggest that the tested SNPs may not be associated with susceptibility to acute liver transplant rejection in a Caucasian population.",
keywords = "Adult, Aged, Alleles, CTLA-4 Antigen, European Continental Ancestry Group, Female, Gene Frequency, Genotype, Germany, Graft Rejection, Humans, Liver Transplantation, Male, Middle Aged, Odds Ratio, Polymorphism, Single Nucleotide, Programmed Cell Death 1 Receptor, Retrospective Studies",
author = "Hansj{\"o}rg Thude and Schipler, {Anna Dorothea} and Andras Treszl and Sven Peine and Martina Koch and Martina Sterneck and Bj{\"o}rn Nashan",
note = "Copyright {\textcopyright} 2013 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.",
year = "2013",
month = aug,
day = "1",
doi = "10.1016/j.humimm.2013.04.021",
language = "English",
volume = "74",
pages = "1041--5",
journal = "HUM IMMUNOL",
issn = "0198-8859",
publisher = "Elsevier Inc.",
number = "8",

}

RIS

TY - JOUR

T1 - Lack of association between CTLA-4 and PDCD1 polymorphisms and acute rejection in German liver transplant recipients

AU - Thude, Hansjörg

AU - Schipler, Anna Dorothea

AU - Treszl, Andras

AU - Peine, Sven

AU - Koch, Martina

AU - Sterneck, Martina

AU - Nashan, Björn

N1 - Copyright © 2013 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.

PY - 2013/8/1

Y1 - 2013/8/1

N2 - Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and programmed cell-death 1 (PDCD1) are two genes encoding coinhibitory immunoreceptors that are involved in regulation transplant rejection and tolerance induction. Thus, CTLA-4 and PDCD1 may be good candidate genes to evaluate in liver transplant rejection. In this retrospective study, we investigated whether four functional single nucleotide polymorphisms (SNP) of the CTLA-4 gene and PDCD1 gene were associated with susceptibility to liver transplant rejection. The SNPs -1772T>C (rs733618), -1661A>G (rs4553808) of the CTLA-4 gene, and the SNPs 7146G>A (rs11568821), 7209C>T (rs41386349) of the PDCD1 gene were genotyped by polymerase chain reaction allele specific restriction enzyme analysis (PCR-ASRA) in 100 liver recipients with acute rejection, 104 liver transplant recipients without acute rejection and 100 healthy control individuals. For the selected SNPs we did not detect any significant difference in genotypic and allelic frequencies between liver transplant recipients with and without acute rejection. In conclusion, our results suggest that the tested SNPs may not be associated with susceptibility to acute liver transplant rejection in a Caucasian population.

AB - Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and programmed cell-death 1 (PDCD1) are two genes encoding coinhibitory immunoreceptors that are involved in regulation transplant rejection and tolerance induction. Thus, CTLA-4 and PDCD1 may be good candidate genes to evaluate in liver transplant rejection. In this retrospective study, we investigated whether four functional single nucleotide polymorphisms (SNP) of the CTLA-4 gene and PDCD1 gene were associated with susceptibility to liver transplant rejection. The SNPs -1772T>C (rs733618), -1661A>G (rs4553808) of the CTLA-4 gene, and the SNPs 7146G>A (rs11568821), 7209C>T (rs41386349) of the PDCD1 gene were genotyped by polymerase chain reaction allele specific restriction enzyme analysis (PCR-ASRA) in 100 liver recipients with acute rejection, 104 liver transplant recipients without acute rejection and 100 healthy control individuals. For the selected SNPs we did not detect any significant difference in genotypic and allelic frequencies between liver transplant recipients with and without acute rejection. In conclusion, our results suggest that the tested SNPs may not be associated with susceptibility to acute liver transplant rejection in a Caucasian population.

KW - Adult

KW - Aged

KW - Alleles

KW - CTLA-4 Antigen

KW - European Continental Ancestry Group

KW - Female

KW - Gene Frequency

KW - Genotype

KW - Germany

KW - Graft Rejection

KW - Humans

KW - Liver Transplantation

KW - Male

KW - Middle Aged

KW - Odds Ratio

KW - Polymorphism, Single Nucleotide

KW - Programmed Cell Death 1 Receptor

KW - Retrospective Studies

U2 - 10.1016/j.humimm.2013.04.021

DO - 10.1016/j.humimm.2013.04.021

M3 - SCORING: Journal article

C2 - 23628397

VL - 74

SP - 1041

EP - 1045

JO - HUM IMMUNOL

JF - HUM IMMUNOL

SN - 0198-8859

IS - 8

ER -