Skip to main navigation Skip to search Skip to main content

International standards for minimum potency of anti-A and anti-B blood grouping reagents: Evaluation of candidate preparations in an international collaborative study

  • S. J. Thorpe*
  • , B. Fox
  • , A. B. Heath
  • , M. Scott
  • , M. de Haas
  • , S. Kochman
  • , A. Padilla
  • *Corresponding author for this work
  • Medicines and Healthcare Products Regulatory Agency
  • NHS Blood and Transplant
  • Sanquin Blood Supply Foundation
  • United States Food and Drug Administration
  • World Health Organization

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background and Objectives: The aim of the study was to evaluate lyophilized monoclonal IgM anti-A and anti-B preparations for use as international standards (IS) to specify recommended minimum potencies of anti-A and anti-B blood grouping reagents in tube tests. Materials and Methods: The candidate IS for minimum potency of anti-A and anti-B blood grouping reagents, codes 03/188 and 03/164, respectively, were evaluated against a wide range of commercial anti-A and anti-B blood grouping reagents in an international collaborative study involving 16 laboratories in nine countries. Laboratories titrated 03/188 and 03/164 in parallel with as many commercial anti-A and anti-B blood grouping reagents, respectively, as were available to them, in tube tests according to specified haemagglutination methodology. Three of these laboratories and a further laboratory also titrated 03/188 and 03/164 in parallel with currently available reference preparations for anti-A and anti-B. The ratios of the mean endpoint titres of the anti-A and anti-B reagents to those of 03/188 and 03/164, respectively, within each laboratory were calculated. Results: The ratios of the mean titres of the anti-A reagents to the mean titre of 03/188 within a laboratory fell within 0·062 and 4, i.e. the potencies of the anti-A reagents were between a sixteenth to four times as strong as 03/188. The ratios of the mean titres of the anti-B reagents to the mean titre of 03/164 within a laboratory also fell within 0·062 and 4, with one outlier. Conclusions: By international consensus, a 1 in 8 dilution of the candidate IS for anti-A, 03/188, and a 1 in 4 dilution of the candidate IS for anti-B, 03/164, were considered appropriate to define the recommended minimum potencies of anti-A and anti-B blood grouping reagents, respectively, in tube tests. On the basis of these results, preparations 03/188 and 03/164 were established by the World Health Organization as International Standards for Minimum Potency of Anti-A and Anti-B Blood Grouping Reagents respectively, and by the US Food and Drug Administration Center for Biologics Evaluation and Research as Minimum Potency Reference Reagents. © 2006 Blackwell Publishing Ltd.
Original languageEnglish
Pages (from-to)336-344
JournalVox sanguinis
Volume91
Issue number4
DOIs
Publication statusPublished - Nov 2006
Externally publishedYes

Fingerprint

Dive into the research topics of 'International standards for minimum potency of anti-A and anti-B blood grouping reagents: Evaluation of candidate preparations in an international collaborative study'. Together they form a unique fingerprint.

Cite this