In vitro Quality of Platelets with Low Plasma Carryover Treated with Ultraviolet C Light for Pathogen Inactivation

被引:23
|
作者
Johnson, Lacey [1 ]
Hyland, Ryan [1 ]
Tan, Shereen [1 ]
Tolksdorf, Frank [2 ]
Sumian, Chryslain [3 ]
Seltsam, Axel [4 ]
Marks, Denese [1 ]
机构
[1] Australian Red Cross Blood Serv, Res & Dev, Sydney, NSW, Australia
[2] MacoPharma Int GmbH, Langen, Germany
[3] MacoPharma, Tourcoing, France
[4] German Red Cross Blood Serv NSTOB, Springe, Germany
关键词
UVC; Pathogen inactivation; Platelet concentrates; Plasma carryover; ADDITIVE SOLUTION; BLOOD COMPONENTS; REDUCTION; SYSTEM; MICROPARTICLES; IRRADIATION; STORAGE; UV; UPDATE; PHASE;
D O I
10.1159/000441830
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The THERAFLEX UV-Platelets system uses shortwave ultraviolet C light (UVC, 254 nm) to inactivate pathogens in platelet components. Plasma carryover influences pathogen inactivation and platelet quality following treatment. The plasma carryover in the standard platelets produced by our institution are below the intended specification (< 30%). Methods: A pool and split study was carried out comparing untreated and UVC-treated platelets with < 30% plasma carryover (n = 10 pairs). This data was compared to components that met specifications (> 30% plasma). The platelets were tested over storage for in vitro quality. Results: Platelet metabolism was accelerated following UVC treatment, as demonstrated by increased glucose consumption and lactate production. UVC treatment caused increased externalization of phosphatidylserine on platelets and microparticles, activation of the GPIIb/ IIIa receptor (PAC-1 binding), and reduced hypotonic shock response. Platelet function, as measured with thrombelastogram, was not affected by UVC treatment. Components with < 30% plasma were similar to those meeting specification with the exception of enhanced glycolytic metabolism. Conclusion: This in vitro analysis demonstrates that treatment of platelets with < 30% plasma carryover with the THERAFLEX UV-Platelets system affects some aspects of platelet metabolism and activation, although in vitro platelet function was not negatively impacted. This study also provides evidence that the treatment specifications of plasma carryover could be extended to below 30%. (C) 2015 S. Karger GmbH, Freiburg
引用
收藏
页码:190 / 197
页数:8
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