Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2018 Dec 31;13(12):e0210099.
doi: 10.1371/journal.pone.0210099. eCollection 2018.

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

Affiliations
Clinical Trial

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

Jonas Sawierucha et al. PLoS One. .

Abstract

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-Lua 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.

PubMed Disclaimer

Conflict of interest statement

This work was supported by Bio-Rad DiaMed. This does not alter the adherence to all PLOS ONE policies on sharing data and materials.

Similar articles

Cited by

References

    1. Schonewille H, Honohan A, van der Watering LM, Hudig F, Te Boekhorst PA, Koopman-van Gemert AW, et al. Incidence of alloantibody formation after ABO-D or extended matched red blood cell transfusions: a randomized trial (MATCH study). Transfusion. 2016;56(2):311–20. Epub 2015/10/08. 10.1111/trf.13347 - DOI - PubMed
    1. Ahrens N, Pruss A, Kähne A, Kiesewetter H, Salama A. Coexistence of autoantibodies and alloantibodies to red blood cells due to blood transfusion. Transfusion. 2007;47(5):813–6. Epub 2007/05/01. 10.1111/j.1537-2995.2007.01194.x - DOI - PubMed
    1. Schonewille H, Haak HL, van Zijl AM. RBC antibody persistence. Transfusion. 2000;40(9):1127–31. Epub 2000/09/16. 10.1046/j.1537-2995.2000.40091127.x - DOI - PubMed
    1. Reverberi R. The persistence of red cell alloantibodies. Blood Transfus. 2008;6(4):225–34. Epub 2008/12/31. 10.2450/2008.0021-08 - DOI - PMC - PubMed
    1. Tormey CA, Stack G. The persistence and evanescence of blood group alloantibodies in men. Transfusion. 2009;49(3):505–12. Epub 2008/12/02. 10.1111/j.1537-2995.2008.02014.x - DOI - PubMed

Publication types