Volume 87, Issue 4 pp. 250-256

Development of white blood cell fragments, during the preparation and storage of platelet concentrates, as measured by using real-time polymerase chain reaction

M. J. Dijkstra-Tiekstra

Corresponding Author

M. J. Dijkstra-Tiekstra

Sanquin Blood Bank North-west Region, Amsterdam, the Netherlands

Correspondence: M. J. Dijkstra-Tiekstra, Sanquin Blood Bank North-west Region, Plesmanlaan 125, 1066 CX Amsterdam, PO Box 9137, 1006 AC Amsterdam, the Netherlands
E-mail: [email protected]Search for more papers by this author
C. E. Van Der Schoot

C. E. Van Der Schoot

Sanquin Research, Amsterdam, the Netherlands

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R. N. I. Pietersz

R. N. I. Pietersz

Sanquin Blood Bank North-west Region, Amsterdam, the Netherlands

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P. C. Huijgens

P. C. Huijgens

VU medical centre, Department of Hematology, Amsterdam, the Netherlands

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P. F. Van Der Meer

P. F. Van Der Meer

Sanquin Blood Bank North-west Region, Amsterdam, the Netherlands

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H. W. Reesink

H. W. Reesink

Sanquin Blood Bank North-west Region, Amsterdam, the Netherlands

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First published: 07 December 2004
Citations: 7

Abstract

Background and Objectives White blood cell (WBC) fragments may cause human leucocyte antigen (HLA) immunization in recipients. We investigated the occurrence and production of WBC fragments in platelet concentrates (PCs) and plasma units, during storage and filtration, by using real-time polymerase chain reaction (PCR) and flow cytometry.

Materials and Methods To study the occurrence of WBC fragments, ‘male’ WBCs were spiked into double-filtered ‘female’ PCs in a concentration series of 0·03–100 WBCs/µl (n = 4 per level). To study the production of WBC fragments, ‘male’ WBCs were spiked into ‘female’ plasma units to 4 × 109 WBCs/l and stored at room temperature prior to filtration (n = 4 per storage time; t = 0, 24 or 48 h). DNA was measured by both albumin real-time PCR and Y real-time PCR. Intact WBCs were counted by using flow cytometry. The number of WBC fragments was calculated by subtracting cell-free DNA (real-time PCR on supernatant) and intact WBCs (flow cytometry) from the total DNA amount (real-time PCR).

Results Spiking of ‘male’ WBCs into ‘female’ PCs showed that the Y real-time PCR is linear and has a reproducible quantitative range down to 0·03 WBC/µl, but that the albumin-PCR, in unspiked samples, revealed a total of 6–10 WBC equivalents/µl (eq/µl). After centrifugation, half of this was observed as cell-free DNA in the supernatant, suggesting that the remaining DNA is derived from WBC fragments. The number of intact WBCs, amount of cell-free DNA and number of WBC fragments after filtration increased significantly when filtration was delayed for up to 48 h, from 0·1 WBC/µl, 1·3 WBC eq/µl and 0·6 WBC eq/µl at t = 0 h to 25 WBC/µl, 38 WBC eq/µl and 57 WBC eq/µl at t = 48 h, respectively.

Conclusions WBC fragments occur in WBC-reduced PCs and increase when products are stored, prior to filtration, up to levels that are equivalent to the amounts of intact WBCs that induce HLA immunization (i.e. > 5 × 106/unit).

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