Volume 44, Issue 5 pp. 868-874
ORIGINAL ARTICLE

Validation of a single tube 3-colour immature red blood cell screening assay for the detection and enumeration of small, medium and large paroxysmal nocturnal haemoglobinuria clones by flow cytometry

Iuri Marinov

Corresponding Author

Iuri Marinov

Clinical Department, Institute of Haematology and Blood Transfusion, Prague, Czech Republic

Correspondence

Iuri Marinov, Institute of Haematology and Blood Transfusion, U nemocnice 1, 128 20, Prague 2, Czech Republic.

Email: [email protected]

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Stephen J. Richards

Stephen J. Richards

Division of Haematology and Immunology, Leeds Institute of Medical Research at St James's, University of Leeds, Leeds, UK

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Adam Pešek

Adam Pešek

Clinical Department, Institute of Haematology and Blood Transfusion, Prague, Czech Republic

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Andrea J. Illingworth

Andrea J. Illingworth

Dahl-Chase Diagnostic Services, Bangor, Maine, USA

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D. Robert Sutherland

D. Robert Sutherland

Department of Laboratory Medicine, Toronto General Hospital, Toronto, Ontario, Canada

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First published: 25 May 2022
Citations: 2

Abstract

Introduction

The reliable diagnosis of paroxysmal nocturnal haemoglobinuria (PNH) by flow cytometry is based on mandatory analysis of the erythroid, neutrophilic and monocytic lineages. In this study, we have evaluated the performance characteristics of a recently published immature red blood cell (iRBC) assay as a potential screening test for PNH by flow cytometry.

Methods

Intra- and inter-assay imprecision were determined in five replicates of small, medium and large PNH iRBC clones. Analytical and functional sensitivity was assessed by performing spiking tests for five replicates. Thirty healthy donors and 441 PNH patients were tested for evaluation of clinical specificity, sensitivity, positive and negative predictive values.

Results

Coefficients of variation (CV) for intra-/inter-assay imprecision analyses were 1.31/1.50, 3.19/2.61 and 3.99/1.58 for the big, medium and small clone sizes, respectively. Absolute values (100%) were found for both clinical specificity and sensitivity as well as for both positive and negative predictive values. The CV from 5 replicate results for 10 clustered events was 15.7%. The coefficient of determination (r2), Pearson's correlation coefficient (r) and Bland–Altman mean bias were 0.9436/0.9234/1.7 for PNH iRBC compared to PNH neutrophils and 0.9553/0.9387/2.1 for PNH iRBCs compared to PNH monocytes.

Conclusion

Our results confirm very good performance characteristics, high analytical and functional sensitivity, absolute clinical specificity and sensitivity as well as favourable correlation between PNH iRBCs and both PNH neutrophils and monocytes, suggesting that this cost-effective 3-colour iRBC assay can be used as a reliable screening test for evaluation of small, medium and large PNH clones by flow cytometry.

CONFLICT OF INTEREST

The authors have no competing interests.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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