BACKGROUND: In the event of hemorrhage and blood loss, platelets play
a vital role in the coagulation process. However. there are currently
no acceptable protocols far long-term storage of platelets. As a first
step toward testing the efficacy of stored platelets or platelet subs
titutes in vivo, a flow cytometric technique was developed to detect h
uman platelets in rabbit blood. STUDY DESIGN AND METHODS: Human platel
ets were transfused to rabbits whose reticuloendothelial system was in
hibited by the administration of ethyl palmitate. Because human and ra
bbit platelets display surface molecules with different epitopes, huma
n platelets were selectively labeled with antibodies specific for glyc
oprotein IX (CD42a). As this antibody does not label rabbit platelets,
it allows discrimination of human from rabbit platelets in samples of
rabbit blood containing both types of platelets. RESULTS: Survival of
human platelets in rabbits was monitored by flow cytometry and fluore
scence microscopy in blood drawn at various times after the platelet t
ransfusion. Fresh human platelets transfused to untreated control rabb
its (n = 3) were removed from circulation within 10 minutes of the com
pletion of the transfusion. Fresh platelets (1 day old) transfused to
rabbits treated with ethyl palmitate (n = 5) survived for 24 hours wit
h an average half-life of 8.6 hours. In contrast, 8-day-old platelets
were cleared from the circulation sooner with an average half-life of
2.9 hours (n = 4). CONCLUSION: This report describes a rapid and effic
ient method of assessing the survival of human platelets in a rabbit m
odel using flow cytometry. This technique will enable.the monitoring i
n rabbits of human platelets prepared by various preservation protocol
s.