Literature DB >> 35611383

Application of Blood Group Genotyping by Next-Generation Sequencing in Various Immunohaematology Cases.

Tae Yeul Kim1, HongBi Yu2, Minh-Trang Thi Phan3, Ja-Hyun Jang1, Duck Cho1,2,3,4.   

Abstract

Background: Next-generation sequencing (NGS) technology has been recently introduced into blood group genotyping; however, there are few studies using NGS-based blood group genotyping in real-world clinical settings. In this study, we applied NGS-based blood group genotyping into various immunohaematology cases encountered in routine clinical practice.
Methods: This study included 4 immunohaematology cases: ABO subgroup, ABO chimerism, antibody to a high-frequency antigen (HFA), and anti-CD47 interference. We designed a hybridization capture-based NGS panel targeting 39 blood group-related genes and applied it to the 4 cases.
Results: NGS analysis revealed a novel intronic variant (NM_020469.3:c.29-10T>G) in a patient with an Ael phenotype and detected a small fraction of ABO*A1.02 (approximately 3-6%) coexisting with the major genotype ABO*B.01/O.01.02 in dizygotic twins. In addition, NGS analysis found a homozygous stop-gain variant (NM_004827.3:c.376C>T, p.Gln126*; ABCG2*01N.01) in a patient with an antibody to an HFA; consequently, this patient's phenotype was predicted as Jr(a-). Lastly, blood group phenotypes predicted by NGS were concordant with those determined by serology in 2 patients treated with anti-CD47 drugs.
Conclusion: NGS-based blood group genotyping can be used for identifying ABO subgroup alleles, low levels of blood group chimerism, and antibodies to HFAs. Furthermore, it can be applied to extended blood group antigen matching for patients treated with anti-CD47 drugs.
Copyright © 2021 by S. Karger AG, Basel.

Entities:  

Keywords:  ABO subgroup; Anti-CD47 interference; Chimerism; Next-generation sequencing; Rare blood group

Year:  2021        PMID: 35611383      PMCID: PMC9082207          DOI: 10.1159/000517565

Source DB:  PubMed          Journal:  Transfus Med Hemother        ISSN: 1660-3796            Impact factor:   4.040


  43 in total

1.  Monoclonal anti-CD47 interference in red cell and platelet testing.

Authors:  Randall W Velliquette; Judith Aeschlimann; Julie Kirkegaard; Gayane Shakarian; Christine Lomas-Francis; Connie M Westhoff
Journal:  Transfusion       Date:  2018-12-05       Impact factor: 3.157

2.  Missense mutations outside the catalytic domain of the ABO glycosyltransferase can cause weak blood group A and B phenotypes.

Authors:  Axel Seltsam; Rainer Blasczyk
Journal:  Transfusion       Date:  2005-10       Impact factor: 3.157

3.  Introduction of a real-time-based blood-group genotyping approach.

Authors:  H Polin; M Danzer; J Pröll; K Hofer; U Heilinger; A Zopf; C Gabriel
Journal:  Vox Sang       Date:  2008-05-28       Impact factor: 2.144

4.  A novel mutation +5904 C>T of RUNX1 site in the erythroid cell-specific regulatory element decreases the ABO antigen expression in Chinese population.

Authors:  Y Ying; X Hong; X Xu; K Ma; J He; F Zhu
Journal:  Vox Sang       Date:  2018-07-05       Impact factor: 2.144

5.  Targeted exome sequencing designed for blood group, platelet, and neutrophil antigen investigations: Proof-of-principle study for a customized single-test system.

Authors:  Eileen Roulis; Elizna Schoeman; Matthew Hobbs; Greg Jones; Mark Burton; Gail Pahn; Yew-Wah Liew; Robert Flower; Catherine Hyland
Journal:  Transfusion       Date:  2020-07-20       Impact factor: 3.157

6.  A preliminary evaluation of next-generation sequencing as a screening tool for targeted genotyping of erythrocyte and platelet antigens in blood donors.

Authors:  Agnieszka Orzińska; Katarzyna Guz; Michał Mikula; Maria Kulecka; Anna Kluska; Aneta Balabas; Monika Pelc-Kłopotowska; Jerzy Ostrowski; Ewa Brojer
Journal:  Blood Transfus       Date:  2017-03-10       Impact factor: 3.443

Review 7.  ID CORE XT as a tool for molecular red blood cell typing.

Authors:  Carolina Bonet Bub; Lilian Castilho
Journal:  Expert Rev Mol Diagn       Date:  2019-08-23       Impact factor: 5.225

8.  Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study.

Authors:  William J Lane; Connie M Westhoff; Nicholas S Gleadall; Maria Aguad; Robin Smeland-Wagman; Sunitha Vege; Daimon P Simmons; Helen H Mah; Matthew S Lebo; Klaudia Walter; Nicole Soranzo; Emanuele Di Angelantonio; John Danesh; David J Roberts; Nick A Watkins; Willem H Ouwehand; Adam S Butterworth; Richard M Kaufman; Heidi L Rehm; Leslie E Silberstein; Robert C Green
Journal:  Lancet Haematol       Date:  2018-05-17       Impact factor: 18.959

9.  Weak blood group B phenotypes may be caused by variations in the CCAAT-binding factor/NF-Y enhancer region of the ABO gene.

Authors:  Axel Seltsam; Franz F Wagner; Daniela Grüger; Christa D Gupta; Christina Bade-Doeding; Rainer Blasczyk
Journal:  Transfusion       Date:  2007-08-30       Impact factor: 3.157

10.  Human complement receptor type 1 (CR1) protein levels and genetic variants in chronic Chagas Disease.

Authors:  Thaisa Lucas Sandri; Kárita Cláudia Freitas Lidani; Fabiana Antunes Andrade; Christian G Meyer; Peter G Kremsner; Iara J de Messias-Reason; Thirumalaisamy P Velavan
Journal:  Sci Rep       Date:  2018-01-11       Impact factor: 4.379

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