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Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations

PURPOSE: Co(a) and Co(b) antigens of the Colton (CO) blood group system are implicated in acute and delayed hemolytic transfusion reactions (HTRs). Owing to the inadequate supply of specific antiserum, data on CO phenotypes remain limited. This study aimed to develop genotyping methods to predict Co...

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Autores principales: Nathalang, Oytip, Asisathaporn, Kamonchanok, Intharanut, Kamphon, Chaibangyang, Wanlapa, Leetrakool, Nipapan, Mitundee, Supattra, Bejrachandra, Sasitorn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942508/
https://www.ncbi.nlm.nih.gov/pubmed/36825218
http://dx.doi.org/10.2147/JBM.S398720
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author Nathalang, Oytip
Asisathaporn, Kamonchanok
Intharanut, Kamphon
Chaibangyang, Wanlapa
Leetrakool, Nipapan
Mitundee, Supattra
Bejrachandra, Sasitorn
author_facet Nathalang, Oytip
Asisathaporn, Kamonchanok
Intharanut, Kamphon
Chaibangyang, Wanlapa
Leetrakool, Nipapan
Mitundee, Supattra
Bejrachandra, Sasitorn
author_sort Nathalang, Oytip
collection PubMed
description PURPOSE: Co(a) and Co(b) antigens of the Colton (CO) blood group system are implicated in acute and delayed hemolytic transfusion reactions (HTRs). Owing to the inadequate supply of specific antiserum, data on CO phenotypes remain limited. This study aimed to develop genotyping methods to predict Co(a) and Co(b) antigens and to estimate transfusion-induced alloimmunization risks in three Thai blood donor populations. MATERIALS AND METHODS: The study included 2451 blood samples from unrelated healthy Thai blood donors obtained from central, northern, and southern Thailand. DNA sequencing was used to determine the CO*A and CO*B alleles. In-house PCR with sequence-specific primers (PCR-SSP) and high-resolution melting curve (HRM) assays were performed and genotyping results were compared using DNA sequencing. CO*A and CO*B allele frequencies among Thais were determined using PCR-SSP and their frequencies were compared with other populations. The risks of Co(a) and Co(b) transfusion-induced alloimmunization among Thai donor populations were calculated. RESULTS: The validated genotyping results by PCR-SSP and HRM assays agreed with DNA sequencing. The CO*A/CO*A was the most common (100.0, 100.0, and 99.3%), followed by CO*A/CO*B (0.0, 0.0, and 0.7%) among central, northern and southern Thais. Homozygous CO*B/CO*B was not found. The CO*A and CO*B allele frequencies among central Thais significantly differed compared among southern Thais (p < 0.01) but not among northern Thais. Those allele frequencies among Thais were similar to those of Taiwanese, Chinese and Malay-Malaysian populations but not to South Asian, Southeast Asian, Korean, Japanese, Filipino, French Basque, and Maltese populations (p < 0.01). A higher risk of anti-Co(b) production rather than anti-Co(a) production was particularly noted in the southern Thai population. CONCLUSION: This study constitutes the first to determine CO*A and CO*B genotypes using PCR-SSP and HRM assays among Thais and this finding would be beneficial in predicting alloimmunization risk and providing safe transfusions among Thais.
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spelling pubmed-99425082023-02-22 Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations Nathalang, Oytip Asisathaporn, Kamonchanok Intharanut, Kamphon Chaibangyang, Wanlapa Leetrakool, Nipapan Mitundee, Supattra Bejrachandra, Sasitorn J Blood Med Original Research PURPOSE: Co(a) and Co(b) antigens of the Colton (CO) blood group system are implicated in acute and delayed hemolytic transfusion reactions (HTRs). Owing to the inadequate supply of specific antiserum, data on CO phenotypes remain limited. This study aimed to develop genotyping methods to predict Co(a) and Co(b) antigens and to estimate transfusion-induced alloimmunization risks in three Thai blood donor populations. MATERIALS AND METHODS: The study included 2451 blood samples from unrelated healthy Thai blood donors obtained from central, northern, and southern Thailand. DNA sequencing was used to determine the CO*A and CO*B alleles. In-house PCR with sequence-specific primers (PCR-SSP) and high-resolution melting curve (HRM) assays were performed and genotyping results were compared using DNA sequencing. CO*A and CO*B allele frequencies among Thais were determined using PCR-SSP and their frequencies were compared with other populations. The risks of Co(a) and Co(b) transfusion-induced alloimmunization among Thai donor populations were calculated. RESULTS: The validated genotyping results by PCR-SSP and HRM assays agreed with DNA sequencing. The CO*A/CO*A was the most common (100.0, 100.0, and 99.3%), followed by CO*A/CO*B (0.0, 0.0, and 0.7%) among central, northern and southern Thais. Homozygous CO*B/CO*B was not found. The CO*A and CO*B allele frequencies among central Thais significantly differed compared among southern Thais (p < 0.01) but not among northern Thais. Those allele frequencies among Thais were similar to those of Taiwanese, Chinese and Malay-Malaysian populations but not to South Asian, Southeast Asian, Korean, Japanese, Filipino, French Basque, and Maltese populations (p < 0.01). A higher risk of anti-Co(b) production rather than anti-Co(a) production was particularly noted in the southern Thai population. CONCLUSION: This study constitutes the first to determine CO*A and CO*B genotypes using PCR-SSP and HRM assays among Thais and this finding would be beneficial in predicting alloimmunization risk and providing safe transfusions among Thais. Dove 2023-02-17 /pmc/articles/PMC9942508/ /pubmed/36825218 http://dx.doi.org/10.2147/JBM.S398720 Text en © 2023 Nathalang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Nathalang, Oytip
Asisathaporn, Kamonchanok
Intharanut, Kamphon
Chaibangyang, Wanlapa
Leetrakool, Nipapan
Mitundee, Supattra
Bejrachandra, Sasitorn
Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations
title Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations
title_full Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations
title_fullStr Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations
title_full_unstemmed Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations
title_short Genotyping Approach to Predict Co(a) and Co(b) Antigens in Thai Blood Donor Populations
title_sort genotyping approach to predict co(a) and co(b) antigens in thai blood donor populations
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942508/
https://www.ncbi.nlm.nih.gov/pubmed/36825218
http://dx.doi.org/10.2147/JBM.S398720
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