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Release of immune modulation factors from platelet concentrates during storage after photochemical pathogen inactivation treatment
Authors:Cognasse Fabrice  Osselaer Jean-Claude  Payrat Jean Marc  Chavarin Patricia  Corash Laurence  Garraud Olivier
Affiliation:Blood Transfusion Center, EFS Auvergne-Loire, Saint-Etienne, France.
Abstract:BACKGROUND: Blood platelets (PLTs) are critical for hemostasis, and they contain biologically active constituents with the potential to modulate inflammatory responses. This study examined the effects of photochemical pathogen inactivation treatment (PCT) on the release of cytokines and/or chemokines from PLT components. STUDY DESIGN AND METHODS: Double-dose apheresis PLT components were suspended in plasma-PLT additive solution mixtures and divided into paired therapeutic units. One unit served as an untreated control and the other unit was treated with PCT. PLT concentrations, pH, and levels of cytokines and/or chemokines (CD62p, platelet-derived growth factor-AB, interleukin [IL]-8, soluble CD40 ligand [sCD40L], IL-1beta, and tumor necrosis factor alpha) were measured during 7 days of storage in PLT component supernatants and PLT lysates. RESULTS: PLT content, pH, and cytokine and/or chemokine content and release from PLT component prepared with PCT were not different (p > 0.05) from paired control components during storage. Levels of sCD40L, however, increased significantly during storage while decreasing in parallel within PLT lysates, although no differences were detected between paired PCT and control PLT component. CONCLUSION: PCT did not increase the release or secretion of PLT chemokines and/or cytokines over a 7-day period compared to conventional PLT component.
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