Background and Objectives: The presence of contaminating white blood cells
(WBCs) in platelet concentrates is associated with transfusion reactions an
d may adversely alter the quality of platelets during storage. Leukocyte de
pletion by filtration of platelets has been increasingly used to avoid thes
e complications. However, the best time for filtration and the benefits of
filtering single-donor platelet concentrates (thrombapheresis, TH) have yet
to be clearly defined. Methods: In a randomized study of 202 TH collected
with an Autopheresis C system, we determined whether prestorage filtration
(preSF) of WBCs from TH as compared with poststorage (bedside) filtration (
postSF) resulted in a better product. Levels of cytokines and C3a accumulat
ing in the medium during storage, platelet activation state, in vivo platel
et recovery, and transfusion reactions were compared in pre- and poststorag
e products. Results: As compared to preSF, significantly more postSF TH had
detectable levels of tumor necrosis factor-alpha (TNF-alpha; 47 vs. 15%; p
<0.0001) and interleukin 6 (13 vs. 3%; p = 0.02), lower pH (p<0.0001) and d
ecreased levels of C3a (910 vs. 2,000 pg/ml; p<0.0001). Furthermore, platel
et activation was increased in postSF TH (p = 0.022). PostSF TH tended to p
lug the bedside filter (27% of postSF TH delivered) from day 3 onward. Ther
e was also a significant difference in platelet recovery, postSF TH showing
a lower corrected count increment (CCI; p = 0.0055) when taking into accou
nt the postSF TH that plugged filters (CCI = 0), but no difference when plu
gged TH were excluded. A correlation could be established between TNF-a lev
els and poor in vivo recovery (p < 0.0001). Febrile non hemolytic transfusi
on reactions were low in both groups (4 and 9%). Conclusion: These results
indicate a benefit of preSF TH as compared with postSF TH based on the foll
owing parameters: decrease in cytokine levels, less platelet activation, ma
intenance of higher pH, and more efficient use of stored platelets (27% of
postSF TH were lost because of plugging of filters). These results apply pa
rticularly to the Autopheresis C systems with its high initial WBC content.