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首页> 外文期刊>Developments in Biologicals >Reacting to an Emerging Safety Threat: West Nile Virus in North America
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Reacting to an Emerging Safety Threat: West Nile Virus in North America

机译:应对新兴安全威胁:北美的西尼罗河病毒

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West Nile virus (WNV) entered North America in 1999 and in 2002 was shown to be transfusion transmitted. With competent mosquito and bird vectors throughout the United States and Canada, WNV clinical disease continues at epidemic proportions. Due to these facts, blood donor screening was implemented prior to the 2003 mosquito season and occurs using a variety of strategies. A combination of minipool (MP) nucleic acid amplification testing (NAT) during the " non-season," coupled with the conversion to the more sensitive individual donation (ID) NAT in epidemic locations during epidemic times, has been successful in detecting approximately 1500 infected blood donors. Assuming that each donation was infectious and manufactured into 1.45 blood components, testing has therefore prevented close to 2200 recipient infections and potential clinical disease. During this same time, transfusion transmission has occurred from seven MP NAT-nonreactive/ID NAT-reactive units (6 in 2003 and 1 in 2004), or a total of 30 transfusion transmitted cases since WNV has been identified in North America. Because WNV occurs in infected blood donors at low concentrations (i.e., lower viral loads than HIV or HCV with the highest viral load of 580,000 copies/ml observed in a blood donor), a trigger strategy that is used in most of the US consisting of two NAT-reactive donations detected by MP NAT and a frequency of 1 :1000 or greater has been developed. Since the full implementation of the MP to ID NAT trigger strategy, there have been no documented WNV transfusion transmissions. Because WNV is an acute infection that only occurs seasonally, other strategies have been proposed, such as seasonal testing, which has been implemented successfully in Canada (Quebec), coupled with a screening question used in the " non-season " of whether the donor has been in the US during the past 56 days; if so, WNV NAT is performed. WNV is an example of an emergent agent in which a rapid series of interventions has been successful in controlling transmission through blood transfusion.
机译:西尼罗河病毒(WNV)于1999年进入北美,并于2002年证明是通过输血传播的。 WNV临床疾病在美国和加拿大各地都拥有有效的蚊子和鸟类媒介,但仍在流行。由于这些事实,在2003年蚊子季节之前实施了献血者筛查,并使用多种策略进行了筛查。在“非季节”期间将微型池(MP)核酸扩增测试(NAT)结合起来,再加上在流行期间转换到流行地点中较敏感的个人捐赠(ID)NAT,已成功检测到约1500个受感染的献血者。假设每次捐赠都是具有传染性的,并制成1.45血液成分,那么测试就可以防止近2200例受体感染和潜在的临床疾病。在同一时间,从七个MP NAT-非反应性/ ID NAT-反应性单位(2003年为6个,2004年为1个)发生了输血传播,或者自从在北美发现WNV以来总共发生了30例输血传播病例。由于WNV发生在受感染的献血者中时浓度很低(即,比HIV或HCV的病毒载量低,在献血者中观察到的最高病毒载量为580,000拷贝/ ml),因此在美国大部分地区使用的触发策略包括已开发出两个由MP NAT检测到且频率为1:1000或更高的NAT反应性捐赠。自从MP到ID NAT触发策略的全面实施以来,还没有记录的WNV输血传输。由于WNV是仅在季节性发生的急性感染,因此提出了其他策略,例如季节性测试,该策略已在加拿大(魁北克)成功实施,并在供体是否在“非季节”中使用了筛选问题在过去56天内一直在美国;如果是这样,则执行WNV NAT。 WNV是一种新兴药物的例子,其中一系列快速的干预措施已成功地控制了通过输血的传播。

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