Keil Shawn D, Saakadze Natia, Bowen Richard, Newman James L, Karatela Sulaiman, Gordy Paul, Marschner Susanne, Roback John, Hillyer Christopher D
Terumo BCT, Lakewood, Colorado.
Emory University, Atlanta, Georgia.
Transfusion. 2015 Apr;55(4):858-63. doi: 10.1111/trf.12945. Epub 2014 Dec 1.
Two studies were performed to test the effectiveness of riboflavin and ultraviolet (UV) light treatment (Mirasol PRT, Terumo BCT) against murine cytomegalovirus (MCMV). The first study utilized immune-compromised mice to measure the reduction of cell-free MCMV. A second study used a murine model to evaluate the ability of Mirasol PRT to prevent transfusion-transmitted (TT)-MCMV infection.
Human plasma was inoculated with MCMV and then treated with Mirasol PRT. The viral titer was measured using an infectious dose 50% assay in nude mice. Mice were euthanized on Day 10 posttransfusion, and their spleens were tested for the presence of MCMV DNA using polymerase chain reaction (PCR). Mirasol PRT was also evaluated to determine its effectiveness in preventing TT-MCMV in platelets (PLTs) stored in PLT additive solution. PLTs were inoculated with either cell-associated MCMV or cell-free MCMV and then treated with Mirasol PRT. Mice were transfused with treated or untreated product and were euthanized 14 days posttransfusion. Blood and spleens were assayed for MCMV DNA by real-time-PCR.
Using nude mice to titer MCMV, a modest 2.1-log reduction was observed in plasma products after Mirasol PRT treatment. TT-MCMV was not observed in the mouse transfusion model when either cell-free or cell-associated MCMV was treated with Mirasol PRT; MCMV transmission was uniformly observed in mice transfused with untreated PLTs.
These results suggest that using riboflavin and UV light treatment may be able to reduce the occurrence of transmission of human CMV from infectious PLTs and plasma units.
进行了两项研究以测试核黄素和紫外线(UV)光处理(Mirasol PRT,泰尔茂BCT公司)对抗鼠巨细胞病毒(MCMV)的有效性。第一项研究利用免疫受损小鼠来测量无细胞MCMV的减少情况。第二项研究使用小鼠模型来评估Mirasol PRT预防输血传播(TT)-MCMV感染的能力。
用人血浆接种MCMV,然后用Mirasol PRT进行处理。使用在裸鼠中的半数感染剂量测定法测量病毒滴度。在输血后第10天对小鼠实施安乐死,并使用聚合酶链反应(PCR)检测其脾脏中是否存在MCMV DNA。还对Mirasol PRT进行了评估,以确定其在预防储存于血小板添加剂溶液中的血小板(PLT)中TT-MCMV方面的有效性。用细胞相关MCMV或无细胞MCMV接种PLT,然后用Mirasol PRT进行处理。给小鼠输注经处理或未处理的产品,并在输血后14天对其实施安乐死。通过实时PCR检测血液和脾脏中的MCMV DNA。
使用裸鼠对MCMV进行滴度测定时,Mirasol PRT处理后的血浆制品中观察到适度的2.1对数级减少。当用Mirasol PRT处理无细胞或细胞相关MCMV时,在小鼠输血模型中未观察到TT-MCMV;在输注未处理PLT的小鼠中均观察到MCMV传播。
这些结果表明,使用核黄素和紫外线光处理可能能够减少人类CMV从感染性PLT和血浆单位传播的发生。