Literature DB >> 17593287

Molecular genetic blood group typing by the use of PCR-SSP technique.

Martina Prager1.   

Abstract

BACKGROUND: DNA-based methods are useful for enhancing immunohematology typings. Ready-to-use Conformité Européenne (CE)-marked test kits based on polymerase chain reaction with sequence-specific priming (PCR-SSP) have been developed, which enable the examination of weak, unexpected, or unclear serologic findings. DEVELOPMENT AND VALIDATION: Primers were designed according to established mutation databases. Proficiency testing for CE marking was performed in accordance with Directive 98/79EC of the European Parliament and of the Council of October 27, 1998 on in vitro diagnostic medical devices using pretyped in-house and external samples. INTENDED USE: BAGene PCR-SSP kits are in vitro diagnostic devices. Genotyping of ABO and RHD/RHCE as well as HPA and KEL, JK, and FY specificities has to be performed after the conclusion of the serologic determination. APPLICATION: Ready-to-use PCR-SSP typing kits allow the determination of common, rare, or weak alleles of the ABO blood group, Rhesus, and Kell/Kidd/Duffy systems as well as alleles of the human platelet antigens.
RESULTS: The investigations showed clear-cut results in accordance with serology or molecular genetic pretyping.
CONCLUSION: PCR-SSP is a helpful supplementary technique for resolving most of the common problems caused by discrepant or doubtful serologic results, and it is an easy-to-handle robust method. Questionable cases in donor, recipient, and patient typing can be examined with acceptable cost.

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Year:  2007        PMID: 17593287     DOI: 10.1111/j.1537-2995.2007.01311.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  14 in total

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2.  Rapid, single-subject genotyping to predict red blood cell antigen expression.

Authors:  S L Slezak; S Adams; H Lee-Stroka; J E Martin; L Caruccio; D F Stroncek
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3.  Applying molecular immunohaematology to regularly transfused thalassaemic patients in Thailand.

Authors:  Pairaya Rujirojindakul; Willy A Flegel
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4.  ABO genotyping: the quest for clinical applications.

Authors:  Willy A Flegel
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5.  Improved allele-specific PCR technique for Kidd blood group genotyping.

Authors:  Kamphon Intharanut; Rudi Grams; Sasitorn Bejrachandra; Pramote Sriwanitchrak; Oytip Nathalang
Journal:  J Clin Lab Anal       Date:  2013-01       Impact factor: 2.352

6.  The Bloodgen Project of the European Union, 2003-2009.

Authors:  Neil D Avent; Antonio Martinez; Willy A Flegel; Martin L Olsson; Marion L Scott; Núria Nogués; Martin Písăcka; Geoff L Daniels; Eduardo Muñiz-Diaz; Tracey E Madgett; Jill R Storry; Sigrid Beiboer; Petra M Maaskant-van Wijk; Inge von Zabern; Elisa Jiménez; Diego Tejedor; Monica López; Emma Camacho; Goedele Cheroutre; Anita Hacker; Pavel Jinoch; Irena Svobodova; Ellen van der Schoot; Masja de Haas
Journal:  Transfus Med Hemother       Date:  2009-05-28       Impact factor: 3.747

7.  Molecular typing for blood group antigens within 40 min by direct polymerase chain reaction from plasma or serum.

Authors:  Franz F Wagner; Willy A Flegel; Rita Bittner; Andrea Döscher
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Review 8.  Next-Generation Sequencing Technologies in Blood Group Typing.

Authors:  Daniel Fürst; Chrysanthi Tsamadou; Christine Neuchel; Hubert Schrezenmeier; Joannis Mytilineos; Christof Weinstock
Journal:  Transfus Med Hemother       Date:  2019-12-11       Impact factor: 3.747

9.  Defining Blood Group Gene Reference Alleles by Long-Read Sequencing: Proof of Concept in the ACKR1 Gene Encoding the Duffy Antigens.

Authors:  Yann Fichou; Isabelle Berlivet; Gaëlle Richard; Christophe Tournamille; Lilian Castilho; Claude Férec
Journal:  Transfus Med Hemother       Date:  2019-12-11       Impact factor: 3.747

10.  ABO allele-level frequency estimation based on population-scale genotyping by next generation sequencing.

Authors:  Kathrin Lang; Ines Wagner; Bianca Schöne; Gerhard Schöfl; Kerstin Birkner; Jan A Hofmann; Jürgen Sauter; Julia Pingel; Irina Böhme; Alexander H Schmidt; Vinzenz Lange
Journal:  BMC Genomics       Date:  2016-05-20       Impact factor: 3.969

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