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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Polish Society of Experimental and Clinical Immunology
2017
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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. |
format | Online Article Text |
id | pubmed-5820981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Polish Society of Experimental and Clinical Immunology |
record_format | MEDLINE/PubMed |
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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