Changes in patterns of Bradykinin generation during leucocyte filtration of platelet concentrates

Changes in patterns of Bradykinin generation during leucocyte filtration of platelet concentrates

Transfusion and Apheresis Science 24 (2001) 291±292 www.elsevier.com/locate/transci Short communication Changes in patterns of Bradykinin generatio...

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Transfusion and Apheresis Science 24 (2001) 291±292

www.elsevier.com/locate/transci

Short communication

Changes in patterns of Bradykinin generation during leucocyte ®ltration of platelet concentrates J. Seghatchian a,b,*, P. Krailadsiri a,b a

National Blood Service, Colindale Avenue, Colindale, London NW9 5BG, UK National Blood Service, Crescent Drive, Brentwood, Essex CM15 8DP, UK

b

Received 31 January 2001; accepted 13 February 2001

The passage of platelet concentrates through di€erent types of WBC ®lters can lead to variable degrees of activation of kallikrein/kinin system [1±3]. The generation of Bradykinin has been associated with hypotensive reactions in patients receiving angiotensin-converting enzyme inhibitors [4,5]. While the reactions usually occur in the early stage of transfusion, the kinetic of Bradykinin (BK) generation/retention during WBC ®ltration remains unclear. In this respect, it is not known whether the characteristic behaviour of the two types of ®lters in current use are the same. This study was carried out with the following objectives: 1. To compare the e€ect of negatively and positively charged WBC ®lters on Bradykinin (BK) formation, in a sequential sampling model, using platelet concentrates of the same origin. 2. To compare the characteristic properties of ®ltered platelets obtained from the two types of ®lters, in terms of changes in platelet cellular indices. Platelet concentrates were prepared according to the local SOPs. Filtration was carried out under

* Corresponding author. Tel.: +44-208-258-2700; fax: +44208-258-2970. E-mail address: [email protected] (J. Seghatchian).

standard conditions of head pressure as recommended by the manufacturers. Measurement of Bradykinin (BK): A competitive Elisa technique was employed, using a commercial kit (Markit, Japan). Measurement of platelet cellular indices: Sysmex SE9000 was used for the assessment of platelet count (PLT), mean platelet volume (MPV) and platelet large cell ratio (P-LCR). In all cases (N ˆ 6) a hyperbolic pattern of BK generation/retention was observed, with negatively charged ®lters showing higher values of BK (Fig. 1). The level of BK was much higher in apheresis PC as compared to pooled BC±PC. This may be related to the di€erences in ratio of anticoagulation, the nature of storage container and the difference in subpopulation of platelet/leucocytes in various products. Moreover, during ®ltration a sharp decrease in platelet count occurred initially, followed by a slow increase to the original count as ®ltration continued, indicating a saturation phenomenon. Negatively charged ®lters appeared to preferentially retain the large platelet subpopulation and aggregates (Fig. 2). Conclusion: The observed hyperbolic pattern re¯ects a saturation phenomenon, followed by a slow rate displacement of BK as ®ltration

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J. Seghatchian, P. Krailadsiri / Transfusion and Apheresis Science 24 (2001) 291±292

continued. This could be related to the adhesive property of negatively charged platelets and changes in the microenvironment. Both the overall surface charge and the rate of ®ltration may in¯uence the pattern of BK generation/retention [6]. This may account for the controversial reports that the rate of generation/retention of BK on di€erent ®lters is variable. The pattern of changes observed in negatively charged ®lters is relevant to transfusion reactions of similar negatively charged ®lters used as bed site. In this respect, the prestorage ®lters will be bene®cial as BK is known to have a short shelf-life. Fig. 1. A representative pattern of BK generation/retention by negatively and positively charged ®lters in platelets.

References [1] Krailadsiri P, Seghatchian J. Negatively charged leucocyte ®lter signi®cantly enhances kallikrein and thrombin-like activities of platelet concentrates. Thromb Res 1996;83: 469±74. [2] Shiba M, Tadokoro K, Sawanobori M, et al. Activation of the contact system by ®ltration of platelet concentrates with a negatively charged white cell-removal ®lter and measurement of venous blood bradykinin level in patients who received ®ltered platelets. Transfusion 1997;37:457±62. [3] Takahashi TA, Abe H, Hosoda M, et al. Bradykinin generation during ®ltration of platelet concentrates with a white cell-reduction ®lter. Transfusion 1995;35:967. [4] Sano H, Koga Y, Hamasaki K, et al. Anaphylaxis associated with white-cell reduction ®lter. Lancet 1996; 347:1053. [5] Mair B, Leparc GF. Hypotensive reactions associated with platelet transfusions and angiotensin-converting enzyme inhibitors. Vox Sang 1998;74:27±30. [6] Snyder E, Mechanic S, Baril L, Davenport RO. Removal of soluble biologic response modi®ers (complement and chemokines) by a bedside white cell-reduction ®lter. Transfusion 1996;36(8):707±13.

Fig. 2. Changes in platelet count, MPV and large platelet subpopulation subsequent to passage through negatively and positively charged ®lters.