Background: The MNS7 (Mia) is a low-prevalence antigen, associated with GP.Mur hybrid glycophorin is high in Thai populations. Consequently, anti-Mia, particularly anti-Mur caused by alloimmunisation is involved in transfusion medicine. In Thailand, before the first transfusion of transfusion-dependent patients with thalassemia, typing of Mia and Rh antigens is minimally required to provide phenotype-matched donors. A patient with Mia-positive phenotype encoded by GYP*Mur homozygote (do not express GPB, JENU-negative) receiving either Mia-negative or Mia-positive phenotype can produce anti-JENU, leading to difficulty in locating compatible donors. Genotyping for GYP*(B-A-B) hybrid alleles to predict the JENU-negative phenotype is alternatively implemented. This study aimed to predict the JENU-negative phenotype in multitransfused Thai patients using PCR-based coupled DNA sequencing. Methods: Blood samples from 861 multi-transfused Thai patients were included. Mia antigen testing was performed using serology and PCR-sequence-specific primer (PCR-SSP). GYP*(B-A-B) hybrid alleles were analyzed using Sanger DNA sequencing. Only 5 of 68 patients receiving more than 40 red cell units developed alloantibodies. The sequence analysis revealed that 60 of 68 patients carried the GYP*Mur allele, including GYP*Mur/GYPB heterozygotes (86.76%) and the GYP*Mur/GYP*Mur homozygote (1.47%). The remaining 8 patients were GYP*Thai/GYPB heterozygotes (10.29%) and GYP*ThaiII/GYPB heterozygotes (1.47%). The GYP*Bun, GYP*HF, GYP*Hop and GYP*Kip alleles were not observed. One female patient with JENU-negative phenotype received 24 red cell transfusions within one year without alloantibody production, which might be due to the number of red blood cell (RBC) units or her disease status. Conclusions: Concerning this study, multiple transfusions can induce alloantibody production. Therefore, phenotype-match transfusions are beneficial among patients with long-term transfusion therapy, and further investigation of the JENU-negative phenotype is suggested.
Read full abstract- All Solutions
Editage
One platform for all researcher needs
Paperpal
AI-powered academic writing assistant
R Discovery
Your #1 AI companion for literature search
Mind the Graph
AI tool for graphics, illustrations, and artwork
Unlock unlimited use of all AI tools with the Editage Plus membership.
Explore Editage Plus - Support
Overview
2216 Articles
Published in last 50 years
Articles published on Number Of Red Blood Cells
Authors
Select Authors
Journals
Select Journals
Duration
Select Duration
2190 Search results
Sort by Recency