Volume 44, Issue 1 pp. 82-87
ORIGINAL ARTICLE
Free to Read

Measurement of hematopoietic progenitor cells using XN2000 hematology analyzer

Sahimah Al Mamari

Sahimah Al Mamari

Sultan Qaboos University Hospital, Muscat, Oman

Search for more papers by this author
Ahoud Al Saadi

Ahoud Al Saadi

Sultan Qaboos University Hospital, Muscat, Oman

Search for more papers by this author
Rua Al Zaabi

Rua Al Zaabi

Sultan Qaboos University Hospital, Muscat, Oman

Search for more papers by this author
Alshaima Al Jamalani

Alshaima Al Jamalani

Sultan Qaboos University Hospital, Muscat, Oman

Search for more papers by this author
Jamal Al Qassabi

Jamal Al Qassabi

Sultan Qaboos University Hospital, Muscat, Oman

Search for more papers by this author
Anil Pathare

Anil Pathare

Sultan Qaboos University Hospital, Muscat, Oman

Search for more papers by this author
Murtadha Al-Khabori

Corresponding Author

Murtadha Al-Khabori

Sultan Qaboos University, Muscat, Oman

Correspondence

Murtadha Al-Khabori, Department of Hematology, Sultan Qaboos University, PO Box 38, PC 123, Muscat, Oman.

Emails: [email protected]; [email protected]

Search for more papers by this author
First published: 18 August 2021
Citations: 3

Abstract

Introduction

Stem cell enumeration by the hematopoietic progenitor cells (HPC) mode is a novel method available from Sysmex XN2000 hematology analyzer. A small amount of blood (190 μL) is required, and the results are available in a few minutes without manual gating or presample treatment. The present study compares stem cell measurements using XN2000 analyzer HPC mode and FC500 flow cytometry analyzer using peripheral blood (PB) specimens and apheresis products.

Methods

In this prospective study, CD34-positive cell counts were enumerated using an FC500 flow cytometry analyzer and compared with XN2000 Sysmex analyzer (XN-HPC mode) in the same samples. Results were compared using Bland-Altman plots.

Results

A total of 103 samples were used. In the PB samples, the median HPC count and CD34-positive cells were 83.5 × 106/L and 78.0 × 106/L, respectively. The mean Bland-Altman difference was 4.5 × 106/L (Limits: −51.7 to 60.7 × 106/L), with a Pearson's correlation of 0.79. In the apheresis products, the median HPC count and CD34-positive cells were 1468 × 106/L (IQR: 1049 - 1960 × 106/L) and 1327 × 106/L (IQR: 910 - 2001 × 106/L), respectively. The mean Bland-Altman difference was 179.0 × 106/L (Limits: −2022.2 - 2380.2 × 106/L), with a Pearson's correlation of 0.58.

Conclusion

The XN-HPC mode has an excellent correlation and minimal disagreement for stem cell enumeration in PB compared with flow cytometry and could replace it. There is high disagreement in apheresis products, and therefore, the XN-HPC mode cannot be recommended.

CONFLICT OF INTEREST

All authors declare no relevant conflict of interest.

DATA AVAILABILITY STATEMENT

Data is available on request from the authors.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.