Wei Xu1, Mei Zhu2, Bao-Long Wang3, Hong Su4, Min Wang3. 1. Department of Laboratory Medicine, Affiliated Provincial Hospital of Anhui Medical University, Hefei, Anhui, China ; Department of Blood Transfusion, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China. 2. Department of Nuclear Medicine, The Third Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China. 3. Department of Laboratory Medicine, Affiliated Provincial Hospital of Anhui Medical University, Hefei, Anhui, China. 4. Department of Epidemiology & Biostatistics, School of Public Health, Anhui Medical University, Hefei, Anhui, China.
Abstract
BACKGROUND: The D antigen is highly immunogenic, requiring only a small quantity of transfused red blood cells (RBCs) to cause alloimmunization in D- immunocompetent recipients. DEL was reported arousing alloimmunization to true Rh- patients. Molecular studies of the RHD gene have revealed that DEL individuals retain a grossly intact RHD gene or have a portion of RHD in their genomes. Avoiding immunization with clinically important antibodies is a primary objective in transfusion medicine. METHODS: In order to determine whether pregnant DEL women carrying an RhD+ fetus are at risk of anti-D alloimmunization, 808 Rh- pregnant women with a history of gestations or parturitions who regularly visited hospitals for their prenatal anti-D screening and postpartum care from January 2011 to December 2012 were investigated. Samples were analyzed for DEL by PCR with specific primers, PCR-sequence-specific primers (PCR-SSP), reverse transcription-PCR (RT-PCR), PCRrestriction fragment length polymorphism (PCR-RFLP), and by gene sequencing to characterize different alleles. RESULTS: Among the 808 Rh- pregnant women of our sample, 178 (22.0%) were typed as DEL; 168 DEL samples were confirmed to have the RHD (1,227 G>A) allele, 8 DEL samples were characterized by one base mutation of the RHD (3G >A) allele, and the remaining two DEL samples were determined to carry RHD-CE(4-9)-D or RHD-CE(2-5)-D. The observation of allo-anti-D in two prominent D epitope loss cases confirmed the partial nature of these DEL phenotypes. CONCLUSIONS: In conclusion, evidence is provided that different DEL genotypes code either for partial or complete D antigen expression. It is suggested that the use of RhD+ RBCs in complete D antigen DEL patients does not induce adverse reaction.
BACKGROUND: The D antigen is highly immunogenic, requiring only a small quantity of transfused red blood cells (RBCs) to cause alloimmunization in D- immunocompetent recipients. DEL was reported arousing alloimmunization to true Rh- patients. Molecular studies of the RHD gene have revealed that DEL individuals retain a grossly intact RHD gene or have a portion of RHD in their genomes. Avoiding immunization with clinically important antibodies is a primary objective in transfusion medicine. METHODS: In order to determine whether pregnant DEL women carrying an RhD+ fetus are at risk of anti-D alloimmunization, 808 Rh- pregnant women with a history of gestations or parturitions who regularly visited hospitals for their prenatal anti-D screening and postpartum care from January 2011 to December 2012 were investigated. Samples were analyzed for DEL by PCR with specific primers, PCR-sequence-specific primers (PCR-SSP), reverse transcription-PCR (RT-PCR), PCRrestriction fragment length polymorphism (PCR-RFLP), and by gene sequencing to characterize different alleles. RESULTS: Among the 808 Rh- pregnant women of our sample, 178 (22.0%) were typed as DEL; 168 DEL samples were confirmed to have the RHD (1,227 G>A) allele, 8 DEL samples were characterized by one base mutation of the RHD (3G >A) allele, and the remaining two DEL samples were determined to carry RHD-CE(4-9)-D or RHD-CE(2-5)-D. The observation of allo-anti-D in two prominent D epitope loss cases confirmed the partial nature of these DEL phenotypes. CONCLUSIONS: In conclusion, evidence is provided that different DEL genotypes code either for partial or complete D antigen expression. It is suggested that the use of RhD+ RBCs in complete D antigen DEL patients does not induce adverse reaction.
Entities:
Keywords:
Alloimmunization; Complete DEL; DEL variant; Partial DEL; Pregnant women
Authors: Günther F Körmöczi; Elisabeth Förstemann; Christian Gabriel; Wolfgang R Mayr; Diether Schönitzer; Christoph Gassner Journal: Transfusion Date: 2005-10 Impact factor: 3.157
Authors: Jose R Gonzalez-Porras; Ignacio F Graciani; Jose A Perez-Simon; Jesus Martin-Sanchez; Cristina Encinas; Maria P Conde; Maria J Nieto; Mercedes Corral Journal: Transfusion Date: 2008-04-17 Impact factor: 3.157