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Applications of ultraviolet light in the preparation of platelet concentrates
Author(s) -
Pamphilon D. H.,
Corbin S. A.,
Saunders J.,
Tandy N. P.
Publication year - 1989
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1046/j.1537-2995.1989.29589284134.x
Subject(s) - platelet , blood product , irradiation , ultraviolet light , chemistry , andrology , epinephrine , ultraviolet , immunology , medicine , surgery , materials science , physics , optoelectronics , photochemistry , nuclear physics
Passenger lymphocytes in platelet concentrates (PCs) may induce the formation of lymphocytotoxic antibodies (LCTAbs) and subsequent refractoriness to platelet transfusions. Ultraviolet (UV) irradiation can prevent lymphocytes' acting as stimulator or responder cells in mixed‐lymphocyte reactions (MLRs) and could theoretically prevent LCTAb formation in vivo. A system has been devised for the delivery of UV irradiation to PCs: platelet storage characteristics and MLRs were evaluated in UV‐irradiated PCs harvested from healthy donors with the Haemonetics V50 and PCS cell separators. MLR and response to phytohemagglutinin stimulation were abolished by a dose of 3000 joules per m 2 at a mean wavelength of 310 nm. Platelet aggregatory responses to adenosine diphosphate (ADP), ristocetin, collagen and epinephrine, hypotonic shock response, and pH showed no important differences when control PCs and PCs irradiated as above were compared during 5 days of storage in Fenwal PL‐1240 packs. Lactate production during storage was significantly higher in UV‐treated PCs (p<0.001), but values did not exceed 20 mmol per L. UV transmission at 310 nm in standard blood product containers, including the Fenwal PL‐146, PL‐1240, and PL‐732, was low (<30%), but it was acceptable in the Delmed Cryostorage and DuPont SteriCell packs (>50%). UV irradiation may provide a simple and inexpensive means of producing nonimmunogenic PCs.