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. 2012 Sep;28(3):152-6.
doi: 10.1007/s12288-011-0120-0. Epub 2011 Oct 20.

HLA Antigens Shed from the Surface of Synthetic or Naturally Occurred Platelet-Derived Microparticles During Storage of Platelet Concentrate

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HLA Antigens Shed from the Surface of Synthetic or Naturally Occurred Platelet-Derived Microparticles During Storage of Platelet Concentrate

Fatemeh Yari et al. Indian J Hematol Blood Transfus. 2012 Sep.

Abstract

The demand for standard platelet concentrates (PCs) has continued to increase in the recent years. Infusible platelet membranes (IPM) prepared from new or outdated human platelets have been developed as an alternative to standard PCs, with the additional advantage of long shelf life and increased viral safety. Reduction of HLA antigens on the IPM has been assigned as one of the probable advantages of this product. In re-examining this issue, we studied the existence of HLA class I on the surface of IPM microparticles. In comparison we also surveyed HLA expression on the surface of the naturally occurred platelet-derived microparticles (nPMPs) during 7 days storage. Intended for producing IPM, PCs obtained from Iranian blood transfusion organization were lysed; virally inactivated with wet heat in the presence of a heat stabilizer and then sonicated. IPMs were separated using centrifugation and liquid-stored in 4°C. The expression of HLA class I antigens was surveyed using flow cytometry technique. HLA molecules were present on the microparticles. Shedding of HLA antigens was demonstrated from the surface of the both liquid-stored IPM and nPMPs during storage. Storage of IPM in 4°C was accompanied with significant reduction of HLA molecules. It seemed that achievement of HLA-free IPM could be impossible unless chloroquine treated platelets were used to prepare these microvesicles.

Keywords: HLA class I; IPM; Platelet-derived microparticles.

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Figures

Fig. 1
Fig. 1
Flow cytometry plot. IPM was prepared in 0.25 M concentration of sodium octanoate and liquid-stored in 4°C for 4 months. Expression of HLA class I was analyzed during this time. a The microparticles were gated, b the isotypic control immunoglobulin IgG, c represented the HLA levels in the freshly prepared IPM, d represented the HLA levels in the surface of IPM 1 month after preparation, e represented the HLA levels in the surface of IPM 4 months after preparation

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