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FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft

INTRODUCTION: Fc gamma receptor (FcγR) IIa is considered the most widely distributed of the three classes of Fc receptors, and it expresses an allelic polymorphism. This type of polymorphism may modify the immune response and may be an important factor for some diseases. The aim of the study reporte...

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Autores principales: Fadel, Fatina I., Elshamaa, Manal F., Salah, Ahmed, Elghoroury, Eman A., El-Rahman, Safaa Abd, Ibrahim, Mona Hamed, Kamel, Solaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820981/
https://www.ncbi.nlm.nih.gov/pubmed/29472814
http://dx.doi.org/10.5114/ceji.2017.72817
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author Fadel, Fatina I.
Elshamaa, Manal F.
Salah, Ahmed
Elghoroury, Eman A.
El-Rahman, Safaa Abd
Ibrahim, Mona Hamed
Kamel, Solaf
author_facet Fadel, Fatina I.
Elshamaa, Manal F.
Salah, Ahmed
Elghoroury, Eman A.
El-Rahman, Safaa Abd
Ibrahim, Mona Hamed
Kamel, Solaf
author_sort Fadel, Fatina I.
collection PubMed
description INTRODUCTION: Fc gamma receptor (FcγR) IIa is considered the most widely distributed of the three classes of Fc receptors, and it expresses an allelic polymorphism. This type of polymorphism may modify the immune response and may be an important factor for some diseases. The aim of the study reported herein was to evaluate the association between the FcγRIIa polymorphism and susceptibility to both end-stage renal disease (ESRD) and acute kidney graft rejection (AR) in children who have undergone renal transplantation. MATERIAL AND METHODS: The study evaluated 70 children who had undergone transplantation and 60 healthy subjects. AR was observed in 25 children. RESULTS: FcγRIIa genotypes and alleles were significantly different between transplantation patients and the control group. The assessment for FcγR of the groups in which AR was present showed that there was only a risk of having an acute rejection in homozygous genotype RR. CONCLUSIONS: FcγRIIa RR genotype and allele frequency was increased in paediatric renal transplant recipients. The present findings showed that FcγRIIa genotype may be related to ESRD disease susceptibility, and FcγRIIa polymorphisms seemed to affect AR.
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spelling pubmed-58209812018-02-22 FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft Fadel, Fatina I. Elshamaa, Manal F. Salah, Ahmed Elghoroury, Eman A. El-Rahman, Safaa Abd Ibrahim, Mona Hamed Kamel, Solaf Cent Eur J Immunol Clinical Immunology INTRODUCTION: Fc gamma receptor (FcγR) IIa is considered the most widely distributed of the three classes of Fc receptors, and it expresses an allelic polymorphism. This type of polymorphism may modify the immune response and may be an important factor for some diseases. The aim of the study reported herein was to evaluate the association between the FcγRIIa polymorphism and susceptibility to both end-stage renal disease (ESRD) and acute kidney graft rejection (AR) in children who have undergone renal transplantation. MATERIAL AND METHODS: The study evaluated 70 children who had undergone transplantation and 60 healthy subjects. AR was observed in 25 children. RESULTS: FcγRIIa genotypes and alleles were significantly different between transplantation patients and the control group. The assessment for FcγR of the groups in which AR was present showed that there was only a risk of having an acute rejection in homozygous genotype RR. CONCLUSIONS: FcγRIIa RR genotype and allele frequency was increased in paediatric renal transplant recipients. The present findings showed that FcγRIIa genotype may be related to ESRD disease susceptibility, and FcγRIIa polymorphisms seemed to affect AR. Polish Society of Experimental and Clinical Immunology 2017-12-30 2017 /pmc/articles/PMC5820981/ /pubmed/29472814 http://dx.doi.org/10.5114/ceji.2017.72817 Text en Copyright: © 2017 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Immunology
Fadel, Fatina I.
Elshamaa, Manal F.
Salah, Ahmed
Elghoroury, Eman A.
El-Rahman, Safaa Abd
Ibrahim, Mona Hamed
Kamel, Solaf
FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft
title FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft
title_full FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft
title_fullStr FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft
title_full_unstemmed FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft
title_short FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft
title_sort fcγriia defunctioning polymorphism in paediatric patients with renal allograft
topic Clinical Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820981/
https://www.ncbi.nlm.nih.gov/pubmed/29472814
http://dx.doi.org/10.5114/ceji.2017.72817
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