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用二甲基亚甲基蓝进行灭病毒光处理后红细胞特性的保存

Preservation of red cell properties after virucidal phototreatment with dimethylmethylene blue.

作者信息

Wagner S J, Skripchenko A, Robinette D, Mallory D A, Cincotta L

机构信息

Jerome H. Holland Laboratory for the Biomedical Sciences, American Red Cross, Rockville, Maryland, USA.

出版信息

Transfusion. 1998 Aug;38(8):729-37. doi: 10.1046/j.1537-2995.1998.38898375511.x.

Abstract

BACKGROUND

All published reports have described methods for virus photoinactivation which significantly alter red cell (RBC) properties during storage. In order to improve virucidal activity and reduce damage to RBCs, a series of phenothiazine derivatives were either synthesized or purified and screened for bacteriophage inactivation and red cell potassium efflux. One compound, 1,9-dimethylmethylene blue (dimethyl-methylene blue), had superior screening results and was chosen for further characterization.

STUDY DESIGN AND METHODS

White cell reduced RBC suspensions (30% hematocrit) were deliberately inoculated with extracellular virus or virus-infected VERO cells, incubated with 4 microM dimethyl-methylene blue and illuminated with cool-white fluorescent light. Control and treated samples were titered for virus inactivation. In parallel studies, RBC suspensions were exposed to dimethylmethylene blue and light under identical conditions and assayed for in vitro RBC storage properties.

RESULTS

Phototreatment of RBC suspensions inactivated > 4.4 log10 of extracellular vesicular stomatitis virus (VSV), > 3.0 log10 of intracellular VSV, > 5.0 log10 of extracellular pseudorabies virus (PRV), > 4.8 log10 of intracellular PRV, > 4.7 log10 of extra-cellular bovine virus diarrhea virus, 5.8 log10 of bacterio-phage phi 6 and > 7 log10 of bacteriophage R17. Encephalo-myocarditis virus, a nonenveloped picornavirus, was resistant to photoinactivation. Virucidal conditions resulted in no detectable IgG binding in 11 of 13 samples, unchanged RBC morphology, normal banding patterns of RBC membrane proteins on SDS PAGE, and unaltered characteristics of 12 of 13 RBC antigens during storage as measured by antibody titrations. In addition, minimal changes were observed in RBC osmotic fragility, lysis, potassium efflux, ATP and 2,3-DPG levels, and the strength of one RBC antigen during storage of phototreated samples compared with controls.

CONCLUSION

Dimethylmethylene blue photo-treatment can inactivate several intracellular and extracellular model viruses under conditions which minimally alter RBC properties during 42 days storage at 1-6 degrees C.

摘要

背景

所有已发表的报告都描述了病毒光灭活方法,这些方法在储存过程中会显著改变红细胞(RBC)的特性。为了提高杀病毒活性并减少对红细胞的损伤,合成或纯化了一系列吩噻嗪衍生物,并对其进行噬菌体灭活和红细胞钾外流筛选。一种化合物,1,9-二甲基亚甲蓝(二甲基亚甲蓝),筛选结果优异,被选作进一步表征。

研究设计与方法

将白细胞减少的红细胞悬液(血细胞比容30%)故意接种细胞外病毒或病毒感染的VERO细胞,与4 microM二甲基亚甲蓝孵育,并用冷白色荧光灯照射。对对照和处理后的样品进行病毒灭活滴定。在平行研究中,将红细胞悬液在相同条件下暴露于二甲基亚甲蓝和光下,并检测其体外红细胞储存特性。

结果

红细胞悬液的光处理可灭活>4.4 log10的细胞外水泡性口炎病毒(VSV)、>3.0 log10的细胞内VSV、>5.0 log10的细胞外伪狂犬病病毒(PRV)、>4.8 log10的细胞内PRV、>4.7 log10的细胞外牛病毒性腹泻病毒、5.8 log10的噬菌体phi 6和>7 log10的噬菌体R17。脑心肌炎病毒,一种无包膜的微小核糖核酸病毒,对光灭活有抗性。杀病毒条件导致13个样品中的11个未检测到IgG结合,红细胞形态未改变,SDS-PAGE上红细胞膜蛋白的条带模式正常,通过抗体滴定测量,储存期间13个红细胞抗原中的12个特性未改变。此外,与对照相比,光处理样品储存期间红细胞渗透脆性、溶血、钾外流、ATP和2,3-DPG水平以及一种红细胞抗原的强度变化最小。

结论

在1-6℃下储存42天期间,二甲基亚甲蓝光处理可在最小程度改变红细胞特性的条件下灭活多种细胞内和细胞外模型病毒。

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