Yang Peng, Zhang Xun-Shan, Cheng Yue, Zhao Jun, Wang Ming-Li
Department of Blood Transfusion, Anhui Medical University First Affiliated Hospital, Hefei 230022, Anhui Province, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011 Feb;19(1):227-30.
This study was aimed to evaluate the efficacy of riboflavin photochemical inactivation of virus in red blood cells by using animal models. human cytomegalovirus (HCMV) plus red blood cells were used as indicator, 30 BALA/c mice were divided into the experimental group (n = 10), virus control group (n = 10), visible light control group (n = 5) and red blood cell control group (n = 5). Mice in experimental group were inoculated with red blood cells inactive by the riboflavin photochemical, mice in virus control group was injected with red blood cells without riboflavin photochemical inactivation treatment, and mice in light control group was infused with red blood cells irradiated by visible light, and mice in red blood cells control group was injected with normal red blood cells. The virus was isolated in vitro from mice of various groups, the HCMV UL83 gene was detected by PCR, the PP65 antigen was identified by indirect immunofluorescence. The results indicated that the virus isolation, PCR detection and indirect immunofluorescence identification all showed positive in virus control group and visible light control group, while the results of detection in experimental and red blood cell control groups were negative. It is concluded that riboflavin photochemical viral inactivation of red blood cells is effective.
本研究旨在通过动物模型评估核黄素光化学法对红细胞中病毒的灭活效果。以人巨细胞病毒(HCMV)加红细胞作为指标,将30只BALB/c小鼠分为实验组(n = 10)、病毒对照组(n = 10)、可见光对照组(n = 5)和红细胞对照组(n = 5)。实验组小鼠接种经核黄素光化学法灭活的红细胞,病毒对照组小鼠注射未经核黄素光化学灭活处理的红细胞,可见光对照组小鼠输注经可见光照射的红细胞,红细胞对照组小鼠注射正常红细胞。对各组小鼠进行体外病毒分离,采用PCR检测HCMV UL83基因,通过间接免疫荧光鉴定PP65抗原。结果表明,病毒对照组和可见光对照组的病毒分离、PCR检测及间接免疫荧光鉴定均呈阳性,而实验组和红细胞对照组的检测结果为阴性。结论是核黄素光化学法对红细胞病毒灭活有效。