QUALITY AND SAFETY OF PLATELET APHERESIS CONCENTRATES PRODUCED WITH ANEW LEUKOCYTE REDUCTION SYSTEM

Objectives: Contaminating white blood cells (WBC) in apheresis platele t concentrates (PC) can cause a variety of adverse effects after plate let transfusion. To obtain PCs with low WBC contamination, a new leuko reduction system (LRS) utilizing 'fluidized particle bed' technology h as recently been introduced. Methods: We prospectively examined the ef fect of LRS apheresis on the donor, the quality of the resulting PCs ( n=120), and the platelet increment in the corresponding recipients. Co nventionally prepared apheresis PCs served as control group (n=27). Pl atelet glycoproteins were examined by flow cytometry. Results: In LRS apheresis, we observed no serious adverse effects on the donors, but t he postdonation absolute lymphocyte counts were reduced from 1,787+/-5 05/mu l to 1,405+/-383/mu l (p<0.001). Comparable results were seen in non-LRS donors. The collection efficiency of the LRS procedures was 5 0.0+/-7.6%, resulting in a yield of 4.3+/-1.0x10(11) platelets/PC. In flow cytometry, platelet glycoproteins in LRS PCs were not elevated: m ean fluorescence of CD62 (6+/-4) or CD63 (9+/-3) in comparison with no n-LRS PCs (mean fluorescence of CD62: 7+/-4, CD63: 8+/-3). Median leuk ocyte contamination of the LRS PCs was 0.41x10(5) (range 0.07-8.5) WBC s/unit. In 43 recipients, the 24-hour corrected count increments after transfusion of LRS PCs (12,530+/-8,761) wore essentially the same as those of 20 recipients of non-LRS PCs (13,133+/-9,812; p=0.75). Conclu sions: LRS apheresis appears to be a safe procedure, which produced ef fective PCs with few contaminating leukocytes. With new apheresis tech nology, filtration of PCs may become superfluous.