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Comparison of two column agglutination tests for red blood cell antibody testing

BACKGROUND: Several sensitive methods are available for red blood cell (RBC) antibody screening. Among these, gel and glass card systems have demonstrated comparably good performance in retrospective studies and are widely used in routine patient diagnostics, but their performance in prospective stu...

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Autores principales: Sawierucha, Jonas, Posset, Marion, Hähnel, Viola, Johnson, Christian L., Hutchinson, James A., Ahrens, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312228/
https://www.ncbi.nlm.nih.gov/pubmed/30596807
http://dx.doi.org/10.1371/journal.pone.0210099
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author Sawierucha, Jonas
Posset, Marion
Hähnel, Viola
Johnson, Christian L.
Hutchinson, James A.
Ahrens, Norbert
author_facet Sawierucha, Jonas
Posset, Marion
Hähnel, Viola
Johnson, Christian L.
Hutchinson, James A.
Ahrens, Norbert
author_sort Sawierucha, Jonas
collection PubMed
description BACKGROUND: Several sensitive methods are available for red blood cell (RBC) antibody screening. Among these, gel and glass card systems have demonstrated comparably good performance in retrospective studies and are widely used in routine patient diagnostics, but their performance in prospective studies has not been sufficiently characterised. PATIENTS AND METHODS: Gel card (Bio-Rad DiaMed) and glass bead-based (Ortho Clinical Diagnostics) column agglutination technologies were used to screen for antibodies prospectively (group A) and for antibody identification in stored and fresh samples known to contain RBC antibodies retrospectively (group B). Untreated reagent RBCs and either papain-treated (Bio-Rad) or ficin-treated panel C cells (Ortho) were used for antibody identification. RESULTS: RBC-reactive antibodies were detected in 22 of 1000 group A samples, three of which tested positive only by gel card agglutination, and four only by glass bead agglutination (including one false positive each). Group B comprised 202 sera with known antibodies: 33 of these samples contained 36 antibodies detected only by gel card agglutination, whereas 9 samples contained antibodies detectable only by glass bead-based agglutination. Discrepancies mostly involved weak antibodies reactive by enzyme only. Two sera contained antibody mixtures that neither system detected completely. Of note, in antibody differentiation batches one and two, anti-Lu(a) was reactive in 7 of 7 and 1 of 8 samples, respectively. CONCLUSION: Both column agglutination tests for red cell antibodies had equal sensitivity and specificity with unstored samples. In stored samples, weak and enzyme-only antibodies were more frequently detected with the gel card system.
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spelling pubmed-63122282019-01-08 Comparison of two column agglutination tests for red blood cell antibody testing Sawierucha, Jonas Posset, Marion Hähnel, Viola Johnson, Christian L. Hutchinson, James A. Ahrens, Norbert PLoS One Research Article BACKGROUND: Several sensitive methods are available for red blood cell (RBC) antibody screening. Among these, gel and glass card systems have demonstrated comparably good performance in retrospective studies and are widely used in routine patient diagnostics, but their performance in prospective studies has not been sufficiently characterised. PATIENTS AND METHODS: Gel card (Bio-Rad DiaMed) and glass bead-based (Ortho Clinical Diagnostics) column agglutination technologies were used to screen for antibodies prospectively (group A) and for antibody identification in stored and fresh samples known to contain RBC antibodies retrospectively (group B). Untreated reagent RBCs and either papain-treated (Bio-Rad) or ficin-treated panel C cells (Ortho) were used for antibody identification. RESULTS: RBC-reactive antibodies were detected in 22 of 1000 group A samples, three of which tested positive only by gel card agglutination, and four only by glass bead agglutination (including one false positive each). Group B comprised 202 sera with known antibodies: 33 of these samples contained 36 antibodies detected only by gel card agglutination, whereas 9 samples contained antibodies detectable only by glass bead-based agglutination. Discrepancies mostly involved weak antibodies reactive by enzyme only. Two sera contained antibody mixtures that neither system detected completely. Of note, in antibody differentiation batches one and two, anti-Lu(a) was reactive in 7 of 7 and 1 of 8 samples, respectively. CONCLUSION: Both column agglutination tests for red cell antibodies had equal sensitivity and specificity with unstored samples. In stored samples, weak and enzyme-only antibodies were more frequently detected with the gel card system. Public Library of Science 2018-12-31 /pmc/articles/PMC6312228/ /pubmed/30596807 http://dx.doi.org/10.1371/journal.pone.0210099 Text en © 2018 Sawierucha 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sawierucha, Jonas
Posset, Marion
Hähnel, Viola
Johnson, Christian L.
Hutchinson, James A.
Ahrens, Norbert
Comparison of two column agglutination tests for red blood cell antibody testing
title Comparison of two column agglutination tests for red blood cell antibody testing
title_full Comparison of two column agglutination tests for red blood cell antibody testing
title_fullStr Comparison of two column agglutination tests for red blood cell antibody testing
title_full_unstemmed Comparison of two column agglutination tests for red blood cell antibody testing
title_short Comparison of two column agglutination tests for red blood cell antibody testing
title_sort comparison of two column agglutination tests for red blood cell antibody testing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312228/
https://www.ncbi.nlm.nih.gov/pubmed/30596807
http://dx.doi.org/10.1371/journal.pone.0210099
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