首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Probable transfusion transmission of West Nile virus from an apheresis platelet that screened non‐reactive by individual donor‐nucleic acid testing
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Probable transfusion transmission of West Nile virus from an apheresis platelet that screened non‐reactive by individual donor‐nucleic acid testing

机译:西尼罗河免疫血小板的可能输血传播,筛选单个供体 - 核酸试验的非反应性

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Abstract BACKGROUND Despite West Nile virus (WNV) blood donation screening using nucleic acid testing (NAT), donors with low viral loads not detected by mini‐pool‐NAT have led to transfusion transmitted (TT)‐WNV infection. We describe a probable case of fatal TT‐WNV infection from an individual donor (ID)‐NAT non‐reactive apheresis platelet donation. STUDY DESIGN AND METHODS An apheresis platelet donation was WNV ID‐NAT reactive and prior donations from the same donor were investigated. A WNV ID‐NAT non‐reactive apheresis platelet unit collected 26?days earlier was transfused during heart transplantation to a patient who subsequently developed WNV neuroinvasive disease and expired. The source of the recipient's WNV infection was investigated. RESULTS Twenty‐six days after collection of the suspect platelet unit, a donation from the same donor was WNV ID‐NAT reactive and WNV IgM and IgG positive. In addition to the suspect platelet unit, the heart transplant recipient who developed WNV infection received 17 blood components from 24 donors. Serologic testing performed on 11 of the remaining 24 donors (46%) was WNV IgM negative. Pre‐transplant recipient and heart donor samples tested WNV RNA and IgM negative. CONCLUSION A probable case of fatal neuroinvasive TT‐WNV was linked to an infectious apheresis platelet unit undetected by WNV ID‐NAT. It is hypothesized that the suspect unit was collected early in the viremic period when viral RNA was below the limit‐of‐detection of the ID‐NAT assay. Implementation of ID‐NAT screening of blood donors has not entirely eliminated the risk of TT‐WNV infections, which may best be addressed by pathogen inactivation technologies.
机译:摘要背景尽管西尼罗河病毒(WNV)献血筛选使用核酸试验(NAT),小池NAT未检测到未检测到的病毒载荷的供体导致输血(TT)-WNV感染。我们描述了来自个体供体(ID)的致命TT-WNV感染的可能情况 - 不反应性血吸镜捐献。研究设计和方法采集血小板捐赠是WNV ID-NAT反应性,并研究了来自同一供体的载载物。在随后开发出WNV神经侵蚀性疾病并过期的患者期间,收集了26℃的WNV ID-NAT非反应性血小板血小板单元26?天数在心脏移植到患者。研究了受体的WNV感染的来源。结果26天收集嫌疑人血小板单元后,来自同一供体的捐赠是WNV ID-NAT反应性和WNV IgM和IgG阳性。除嫌疑人血小板单位外,开发WNV感染的心脏移植受体来自24种捐助者的17种血液成分。在剩余的24个供体中的11个(46%)中进行的血清学测试是WnV IgM阴性。移植前受体和心脏供体样品测试WNV RNA和IgM阴性。结论致命的神经侵袭性TT-WNV的可能情况与WNV ID-NAT未被检测的感染性血栓性血小板单元连接。假设当病毒RNA低于ID-NAT测定的探测限制时,嫌疑单位在亚脑病时期收集。献血者ID-NAT筛查的实施并不完全消除了TT-WNV感染的风险,这可能最好通过病原体灭活技术来解决。

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