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MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a)

BACKGROUND: Glycophorin variants of the MNSs blood group are important in Taiwan. For more than 20 years, screening for the most frequent irregular antibody, anti-‘Mi(a)’, has been conducted by using ‘Mi(a)’(+) RBCs, with a significant success. However, the sensitivity and the specificity of this sc...

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Autores principales: Chen, Tai-Di, Chen, Ding-Ping, Wang, Wei-Ting, Sun, Chien-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032321/
https://www.ncbi.nlm.nih.gov/pubmed/24858913
http://dx.doi.org/10.1371/journal.pone.0098166
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author Chen, Tai-Di
Chen, Ding-Ping
Wang, Wei-Ting
Sun, Chien-Feng
author_facet Chen, Tai-Di
Chen, Ding-Ping
Wang, Wei-Ting
Sun, Chien-Feng
author_sort Chen, Tai-Di
collection PubMed
description BACKGROUND: Glycophorin variants of the MNSs blood group are important in Taiwan. For more than 20 years, screening for the most frequent irregular antibody, anti-‘Mi(a)’, has been conducted by using ‘Mi(a)’(+) RBCs, with a significant success. However, the sensitivity and the specificity of this screening strategy have never been validated, and the true incidences of different glycophorin variants in Taiwan have been in controversy. Also, the significance of another less frequent and usually separately reported variant, St(a), has never been evaluated. METHODOLOGY/PRINCIPAL FINDINGS: We ran a population-based screening (from unselected patients in our hospital) for MNSs blood group glycophorin variants by PCR-sequencing method. GP.Mur (Mil.III) was confirmed by sequence from 57 out of 1027 samples (5.6%), and there was no other Miltenberger subtype glycophorin variant found. Glycophorin variant St(a) was found from 35 out of 1027 samples (3.4%). In contrast to anti-‘Mi(a)’, which is the most frequently identified irregular antibody in Taiwan, the prevalence of anti-St(a) was only 0.13% as determined by serologic method. In addition, two new alleles for St(a) were found and reported. CONCLUSION/SIGNIFICANCE: We confirm the long-standing assumption that GP.Mur is the only prevalent Miltenberger subtype in Taiwan. The current anti-‘Mi(a)’ screening method used in Taiwan, although neither sensitive nor specific, is still a suitable practice. Although St(a) antigen has a high prevalence in Taiwan, routine screening for anti-St(a) is not warranted based on current evidence.
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spelling pubmed-40323212014-05-28 MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a) Chen, Tai-Di Chen, Ding-Ping Wang, Wei-Ting Sun, Chien-Feng PLoS One Research Article BACKGROUND: Glycophorin variants of the MNSs blood group are important in Taiwan. For more than 20 years, screening for the most frequent irregular antibody, anti-‘Mi(a)’, has been conducted by using ‘Mi(a)’(+) RBCs, with a significant success. However, the sensitivity and the specificity of this screening strategy have never been validated, and the true incidences of different glycophorin variants in Taiwan have been in controversy. Also, the significance of another less frequent and usually separately reported variant, St(a), has never been evaluated. METHODOLOGY/PRINCIPAL FINDINGS: We ran a population-based screening (from unselected patients in our hospital) for MNSs blood group glycophorin variants by PCR-sequencing method. GP.Mur (Mil.III) was confirmed by sequence from 57 out of 1027 samples (5.6%), and there was no other Miltenberger subtype glycophorin variant found. Glycophorin variant St(a) was found from 35 out of 1027 samples (3.4%). In contrast to anti-‘Mi(a)’, which is the most frequently identified irregular antibody in Taiwan, the prevalence of anti-St(a) was only 0.13% as determined by serologic method. In addition, two new alleles for St(a) were found and reported. CONCLUSION/SIGNIFICANCE: We confirm the long-standing assumption that GP.Mur is the only prevalent Miltenberger subtype in Taiwan. The current anti-‘Mi(a)’ screening method used in Taiwan, although neither sensitive nor specific, is still a suitable practice. Although St(a) antigen has a high prevalence in Taiwan, routine screening for anti-St(a) is not warranted based on current evidence. Public Library of Science 2014-05-23 /pmc/articles/PMC4032321/ /pubmed/24858913 http://dx.doi.org/10.1371/journal.pone.0098166 Text en © 2014 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chen, Tai-Di
Chen, Ding-Ping
Wang, Wei-Ting
Sun, Chien-Feng
MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a)
title MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a)
title_full MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a)
title_fullStr MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a)
title_full_unstemmed MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a)
title_short MNSs Blood Group Glycophorin Variants in Taiwan: A Genotype-Serotype Correlation Study of ‘Mi(a)’ and St(a) with Report of Two New Alleles for St(a)
title_sort mnss blood group glycophorin variants in taiwan: a genotype-serotype correlation study of ‘mi(a)’ and st(a) with report of two new alleles for st(a)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032321/
https://www.ncbi.nlm.nih.gov/pubmed/24858913
http://dx.doi.org/10.1371/journal.pone.0098166
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