The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran

Abstract Introduction The alloimmunization following blood transfusion can be life‐threatening. The Rh alloantibodies are one of the most common causes contributing to alloimmunization. This study aimed to evaluate the rate and causes of alloimmunization and to determine the Rh phenotypes and genoty...

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Main Authors: Mohammad Ali Jalali Far, Arezoo Oodi, Naser Amirizadeh, Mahshid Mohammadipour, Bijan Keikhaei Dehdezi
Format: Article
Language:English
Published: Wiley 2021-03-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
Online Access:https://doi.org/10.1002/mgg3.1614
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author Mohammad Ali Jalali Far
Arezoo Oodi
Naser Amirizadeh
Mahshid Mohammadipour
Bijan Keikhaei Dehdezi
author_facet Mohammad Ali Jalali Far
Arezoo Oodi
Naser Amirizadeh
Mahshid Mohammadipour
Bijan Keikhaei Dehdezi
author_sort Mohammad Ali Jalali Far
collection DOAJ
description Abstract Introduction The alloimmunization following blood transfusion can be life‐threatening. The Rh alloantibodies are one of the most common causes contributing to alloimmunization. This study aimed to evaluate the rate and causes of alloimmunization and to determine the Rh phenotypes and genotypes among sickle cell disease (SCD) and sickle thalassemia (Sβ). Materials and Methods Our study included 104 SCD and Sβ patients referring to Baghaei 2 Hospital of Ahvaz in 2019 using a non‐random simple sampling method. The blood samples were collected for Rh phenotypes, alloantibody screening and identification, and molecular tests. The SSP‐PCR and RFLP methods with the Pst 1 enzyme were used. Results The alloimmunization rate was 9.6% and 13.2% based on immunohematological tests and medical records, respectively. The main alloantibodies (90%) were anti‐Rh, and 40% of the patients had multiple alloantibodies. A significant correlation was found between gender and alloimmunization. The phenotypes of DCce (37.5%), DCcEe (24%), Dce (20.2%), and dce (5.8%) and genotypes of R1r (25%), R1R2 (20.2%), R1R1 (18.3%), and R1R0 (10.6%) were the most prevalent. The R1R2 was a frequent genotype in Sβ. Conclusion R0r′ and R1R0 genotypes were limited to our population in Iran. Due to the differences in RH genotypes between our population and others, the blood transfusion from other ethnicities increased our total alloimmunization rate.
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spelling doaj.art-667b5173a9514fe3983d90fd4fb500032022-12-21T22:33:24ZengWileyMolecular Genetics & Genomic Medicine2324-92692021-03-0193n/an/a10.1002/mgg3.1614The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in IranMohammad Ali Jalali Far0Arezoo Oodi1Naser Amirizadeh2Mahshid Mohammadipour3Bijan Keikhaei Dehdezi4Blood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran IranBlood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran IranBlood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran IranBlood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran IranThalassemia & Hemoglobinopathy Research Center, Research Institute of Health Ahvaz Jundishapur University of Medical Sciences Ahvaz IranAbstract Introduction The alloimmunization following blood transfusion can be life‐threatening. The Rh alloantibodies are one of the most common causes contributing to alloimmunization. This study aimed to evaluate the rate and causes of alloimmunization and to determine the Rh phenotypes and genotypes among sickle cell disease (SCD) and sickle thalassemia (Sβ). Materials and Methods Our study included 104 SCD and Sβ patients referring to Baghaei 2 Hospital of Ahvaz in 2019 using a non‐random simple sampling method. The blood samples were collected for Rh phenotypes, alloantibody screening and identification, and molecular tests. The SSP‐PCR and RFLP methods with the Pst 1 enzyme were used. Results The alloimmunization rate was 9.6% and 13.2% based on immunohematological tests and medical records, respectively. The main alloantibodies (90%) were anti‐Rh, and 40% of the patients had multiple alloantibodies. A significant correlation was found between gender and alloimmunization. The phenotypes of DCce (37.5%), DCcEe (24%), Dce (20.2%), and dce (5.8%) and genotypes of R1r (25%), R1R2 (20.2%), R1R1 (18.3%), and R1R0 (10.6%) were the most prevalent. The R1R2 was a frequent genotype in Sβ. Conclusion R0r′ and R1R0 genotypes were limited to our population in Iran. Due to the differences in RH genotypes between our population and others, the blood transfusion from other ethnicities increased our total alloimmunization rate.https://doi.org/10.1002/mgg3.1614alloimmunizationRH genotypeRh phenotypesickle cell diseasesickle thalassemia
spellingShingle Mohammad Ali Jalali Far
Arezoo Oodi
Naser Amirizadeh
Mahshid Mohammadipour
Bijan Keikhaei Dehdezi
The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran
Molecular Genetics & Genomic Medicine
alloimmunization
RH genotype
Rh phenotype
sickle cell disease
sickle thalassemia
title The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran
title_full The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran
title_fullStr The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran
title_full_unstemmed The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran
title_short The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran
title_sort rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in iran
topic alloimmunization
RH genotype
Rh phenotype
sickle cell disease
sickle thalassemia
url https://doi.org/10.1002/mgg3.1614
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