Ehmann W C, Dancis A, Ferziger R, Karpatkin S
Department of Medicine, New York University Medical School, New York 10016.
Proc Soc Exp Biol Med. 1990 Nov;195(2):192-6. doi: 10.3181/00379727-195-43133.
Three previous articles have reported a PLA1 antigen in the plasma of stored blood which is capable of binding to PLA1-negative platelets in the presence of divalent cations, rendering them PLA1 positive. Such a mechanism could explain the enigma of posttransfusion purpura (PTP), i.e., severe thrombocytopenia in a healthy subject with PLA1-negative platelets secondary to the infusion of blood containing PLA1-positive platelets. We find that the PLA1 antigen of stored blood is due to the presence of platelet fragments which can be removed by centrifugation and that divalent cation-chelating agents play no role in the apparent binding of these fragments to platelets. The apparent conversion of PLA1-negative platelets to the PLA1-positive phenotype by incubation with stored plasma from a PLA1-positive subject is due to the cosedimentation of platelet fragments with the platelets. No soluble PLA1 antigen was found in the plasma of five patients with acute posttransfusion purpura.
此前有三篇文章报道,储存血液的血浆中存在一种PLA1抗原,在二价阳离子存在的情况下,它能够与PLA1阴性血小板结合,使其变为PLA1阳性。这样一种机制可以解释输血后紫癜(PTP)之谜,即健康受试者输注含有PLA1阳性血小板的血液后,出现严重血小板减少,其血小板为PLA1阴性。我们发现,储存血液的PLA1抗原是由于存在血小板碎片,这些碎片可通过离心去除,并且二价阳离子螯合剂在这些碎片与血小板的表面结合中不起作用。通过与PLA1阳性受试者的储存血浆孵育,PLA1阴性血小板表面转变为PLA1阳性表型,这是由于血小板碎片与血小板共同沉降所致。在五例急性输血后紫癜患者的血浆中未发现可溶性PLA1抗原。