Lab Med Online.  2022 Jan;12(1):1-10. 10.47429/lmo.2022.12.1.1.

Development of Cryopreserved Red Blood Cell Panels as Biological Reference Standards for Performance Evaluation of ABO and D Blood Grouping Reagents

Affiliations
  • 1Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea
  • 2Department of Laboratory Medicine, The Catholic University of Korea College of Medicine, Seoul, Korea
  • 3Department of Laboratory Medicine, University of Ulsan College of Medicine, Seoul, Korea

Abstract

Background
Accurate blood typing is essential for blood transfusions, and requires the constant evaluation and maintenance of ABO and D blood grouping reagents. In the present study, we developed cryopreserved red blood cell (RBC) panels and evaluated their feasibility as a standard reference material to verify the quality of ABO and D blood grouping reagents in Korea.
Methods
RBC units obtained from healthy donors were cryopreserved using a high-glycerol method. A total of 400 sets of RBC panels were prepared, composed of blood group A (N=5), B (N=5), O (N=10), AB (N=4), Rh D-positive (N=4), Rh D-negative (N=5), and weak-D (N=1), and 200 sets of RBC subgroup panels composed of A2, A2B, A2B3, A1B3, and B3, and A2, A2B, A2B3, A1B3, and A3B (N=1, each). Quality assessment of the cryopreserved RBC panels before and after cryopreservation was performed by measuring their sensitivity, specificity, avidity, and potency titers.
Results
Our cryopreserved ABO and D RBC panels had a sensitivity and specificity of 100% to existing monoclonal blood grouping reagents, regardless of blood type and cryopreservation time. There were no significant differences in the avidity time and potency titers of the cryopreserved RBCs before and after 6 or 12 months of cryopreservation.
Conclusions
The quality parameters measured here suggest that our newly developed cryopreserved RBC panels were reliable for use as a standard reference material for the performance evaluation of anti-A, -B, and -D blood grouping reagents.

Keyword

Cryopreservation; Red blood cells; Blood grouping reagent; High-glycerol method

Figure

  • Fig. 1 The antigenicity variations observed in cryopreserved RBCs on the day of thawing, and at 1, 3, and 7 days after thawing, according to the preservative used for (A) A antigen, (B) B antigen, (C) D antigen.

  • Fig. 2 The antigenicity variations observed in cryopreserved RBCs on the day of thawing, and at 1, 3, and 7 days after thawing, according to the transportation medium used for (A) A antigen, (B) B antigen, (C) D antigen.


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