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Fatal haemolytic transfusion reaction due to anti-Ena and identification of a novel GYPA c.295delG variant in a Thai family.
Suwanwootichai, Ploymanee; Lopez, Genghis H; Emthip, Morakot; Wilson, Brett; Millard, Glenda M; Onpuns, Sunisa; Laemsri, Kanchana; Bejrachandra, Sasitorn; Liew, Yew-Wah.
Afiliación
  • Suwanwootichai P; Red Cell Reference Laboratory, National Blood Centre, Thai Red Cross Society, Bangkok, Thailand.
  • Lopez GH; Research and Development, Clinical Services and Research, Australian Red Cross Lifeblood, Kelvin Grove, Queensland, Australia.
  • Emthip M; School of Health and Behavioural Sciences, University of the Sunshine Coast, Sippy Downs, Queensland, Australia.
  • Wilson B; Red Cell Reference Laboratory, National Blood Centre, Thai Red Cross Society, Bangkok, Thailand.
  • Millard GM; Red Cell Reference Laboratory, Clinical Services and Research, Australian Red Cross Lifeblood, Kelvin Grove, Queensland, Australia.
  • Onpuns S; Research and Development, Clinical Services and Research, Australian Red Cross Lifeblood, Kelvin Grove, Queensland, Australia.
  • Laemsri K; Red Cell Reference Laboratory, Clinical Services and Research, Australian Red Cross Lifeblood, Kelvin Grove, Queensland, Australia.
  • Bejrachandra S; Transfusion Medicine Unit, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand.
  • Liew YW; Transfusion Medicine Unit, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand.
Vox Sang ; 117(11): 1327-1331, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36102166
ABSTRACT
BACKGROUND AND

OBJECTIVES:

High-frequency antigen Ena (MNS 28) is expressed on glycophorin A (GPA). En(a-) individuals can form anti-Ena 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. 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.

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 Mk Mk RBCs.

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-Ena specificity.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glicoforinas / Reacción a la Transfusión Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glicoforinas / Reacción a la Transfusión Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Año: 2022 Tipo del documento: Article