Kühnel Denis, Müller Sebastian, Pichotta Alexander, Radomski Kai Uwe, Volk Andreas, Schmidt Torben
Virus & Prion Validation Department, Octapharma Biopharmaceuticals GmbH, Frankfurt am Main, Germany.
Transfusion. 2017 Mar;57(3pt2):802-810. doi: 10.1111/trf.13964. Epub 2016 Dec 26.
In 2016 the World Health Organization declared the mosquito-borne Zika virus (ZIKV) a "public health emergency of international concern." ZIKV is a blood-borne pathogen, which therefore causes concerns regarding the safety of human plasma-derived products due to potential contamination of the blood supply. This study investigated the effectiveness of viral inactivation steps used during the routine manufacturing of various plasma-derived products to reduce ZIKV infectivity.
Human plasma and intermediates from the production of various plasma-derived products were spiked with ZIKV and subjected to virus inactivation using the identical techniques (either solvent/detergent [S/D] treatment or pasteurization) and conditions used for the actual production of the respective products. Samples were taken and the viral loads measured before and after inactivation.
After S/D treatment of spiked intermediates of the plasma-derived products Octaplas(LG), Octagam, and Octanate, the viral loads were below the limit of detection in all cases. The mean log reduction factor (LRF) was at least 6.78 log for Octaplas(LG), at least 7.00 log for Octagam, and at least 6.18 log for Octanate after 60, 240, and 480 minutes of S/D treatment, respectively. For 25% human serum albumin (HSA), the mean LRF for ZIKV was at least 7.48 log after pasteurization at 60°C for 120 minutes.
These results demonstrate that the commonly used virus inactivation processes utilized during the production of human plasma and plasma-derived products, namely, S/D treatment or pasteurization, are effective for inactivation of ZIKV.
2016年,世界卫生组织宣布蚊媒传播的寨卡病毒(ZIKV)为“国际关注的突发公共卫生事件”。ZIKV是一种血源性病原体,因此,由于血液供应存在潜在污染,人们对人血浆衍生产品的安全性表示担忧。本研究调查了在各种血浆衍生产品的常规生产过程中使用的病毒灭活步骤对降低ZIKV感染性的有效性。
将寨卡病毒添加到来自各种血浆衍生产品生产过程中的人血浆和中间体中,并使用与实际生产相应产品相同的技术(溶剂/去污剂[S/D]处理或巴氏消毒)和条件进行病毒灭活。在灭活前后采集样本并测量病毒载量。
对血浆衍生产品Octaplas(LG)、Octagam和Octanate的加标中间产物进行S/D处理后,所有情况下病毒载量均低于检测限。在S/D处理60、240和480分钟后,Octaplas(LG)的平均对数减少因子(LRF)至少为6.78 log,Octagam至少为7.00 log,Octanate至少为6.18 log。对于25%人血清白蛋白(HSA),在60°C巴氏消毒120分钟后,ZIKV的平均LRF至少为7.48 log。
这些结果表明,在人血浆和血浆衍生产品生产过程中常用的病毒灭活工艺,即S/D处理或巴氏消毒,对灭活ZIKV是有效的。