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Fatal haemolytic transfusion reaction due to anti-En a and identification of a novel GYPA c.295delG variant in a Thai family.

Authors :
Suwanwootichai P
Lopez GH
Emthip M
Wilson B
Millard GM
Onpuns S
Laemsri K
Bejrachandra S
Liew YW
Source :
Vox sanguinis [Vox Sang] 2022 Nov; Vol. 117 (11), pp. 1327-1331. Date of Electronic Publication: 2022 Sep 14.
Publication Year :
2022

Abstract

Background and Objectives: High-frequency antigen En <superscript>a</superscript> (MNS 28) is expressed on glycophorin A (GPA). En(a-) individuals can form anti-En <superscript>a</superscript> when exposed to GPA. A Thai patient formed an antibody that reacted against all reagent red blood cells (RBCs). The patient received incompatible blood resulting in a fatal haemolytic transfusion reaction (HTR). This study aimed to characterize the antibody detected in the patient and investigate the cause of HTR.<br />Materials and Methods: Blood samples from the patient and three of his family members were investigated. Massively parallel sequencing (MPS) and DNA-microarray were used for genotyping. Standard haemagglutination techniques were used for phenotyping and antibody investigations.<br />Results: DNA sequencing showed the patient was homozygous for GYPA*M c.295delG (p.Val99Ter) predicting En(a-). Three family members were heterozygous for GYPA c.295delG. MPS and DNA-microarray predicted the patient was N- discordant with the N+ RBC phenotype. The patient's plasma was positive with enzyme/chemical-treated reagent RBCs but failed to react with En(a-) and M <superscript>k</superscript> M <superscript>k</superscript> RBCs.<br />Conclusion: The GYPA c.295delG variant prevented GPA expression on RBCs resulting in En(a-) phenotype. The N+ phenotype result was probably due to the anti-N typing reagent detecting 'N' (MNS30) on GPB. The patient's alloantibody has anti-En <superscript>a</superscript> specificity.<br /> (© 2022 International Society of Blood Transfusion.)

Details

Language :
English
ISSN :
1423-0410
Volume :
117
Issue :
11
Database :
MEDLINE
Journal :
Vox sanguinis
Publication Type :
Academic Journal
Accession number :
36102166
Full Text :
https://doi.org/10.1111/vox.13358