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估计人血中变异型克雅氏病的感染滴度。

Estimation of variant Creutzfeldt-Jakob disease infectivity titers in human blood.

机构信息

Division of Emerging and Transfusion-Transmitted Diseases, Office of Blood Research and Review, Rockville, Maryland 20852, USA.

出版信息

Transfusion. 2011 Dec;51(12):2596-602. doi: 10.1111/j.1537-2995.2011.03199.x. Epub 2011 Jun 3.

Abstract

BACKGROUND

Blood of individuals with variant Creutzfeldt-Jakob disease (vCJD) is infectious but the titer is unknown. Current estimates of possible vCJD infectivity titers in blood have largely relied on an assumption that the titers of vCJD agent in human blood are likely to be similar to those in blood of rodents infected with model transmissible spongiform encephalopathy agents, assayed by intracerebral inoculations of rodents of the same species.

STUDY DESIGN AND METHODS

We analyzed published descriptions of experimental transfusion-transmitted (TT) bovine spongiform encephalopathy and scrapie in sheep and reports of TTvCJD in humans, applying statistical approaches to estimate the probable number of intravenous infectious doses (ID(iv) ) per unit of transfused blood (ID(iv) /unit). For humans, ID(iv) /unit of nonleukoreduced red blood cells (NLR-RBCs) were estimated by two statistical models.

RESULTS

Sheep blood collected at or near onset of clinical illness contained a mean of 0.80 ID(iv) /unit. Estimates of infectivity in NLR-RBCs from donors incubating vCJD indicated a probable mean infectivity of 0.29 ID(iv) /unit (Model 1) and 0.75 ID(iv) /unit (Model 2). The analysis predicted a mean of 21 vCJD-infected recipients expected in a cohort transfused with vCJD-implicated NLR-RBCs in the United Kingdom.

CONCLUSION

Our analysis suggested that, while less than one ID(iv ) is likely to be present in a given unit of NLR-RBCs collected from a donor incubating vCJD, there is a high probability of TT infection among recipients of vCJD-implicated blood components. The analysis supports continuing measures currently recommended to reduce the risk of TTvCJD.

摘要

背景

变异型克雅氏病(vCJD)患者的血液具有感染性,但具体滴度未知。目前对血液中 vCJD 感染性滴度的估计主要依赖于一个假设,即 vCJD 病原体在人血中的滴度可能与感染模型传染性海绵状脑病病原体的啮齿动物血液中的滴度相似,通过同种啮齿动物的脑内接种来检测。

研究设计和方法

我们分析了已发表的关于绵羊实验性输血传播(TT)牛海绵状脑病和瘙痒病的描述,以及关于人类 TTvCJD 的报告,应用统计学方法估计每单位输注血液中的可能静脉内感染剂量(ID(iv))(ID(iv)/单位)。对于人类,我们通过两种统计模型估计非白细胞减少性红细胞(NLR-RBC)的 ID(iv)/单位。

结果

在临床发病或接近发病时采集的绵羊血液中,平均含有 0.80 ID(iv)/单位。从潜伏期 vCJD 供体中估计的 NLR-RBC 的感染性,表明可能的平均感染性为 0.29 ID(iv)/单位(模型 1)和 0.75 ID(iv)/单位(模型 2)。分析预测,在英国,用 vCJD 感染的 NLR-RBC 输注一个队列,预计会有 21 名 vCJD 感染的受者。

结论

我们的分析表明,虽然从潜伏期 vCJD 供体采集的每单位 NLR-RBC 中可能存在不到一个 ID(iv),但 vCJD 相关血液成分的受者有很高的 TT 感染概率。该分析支持继续采取目前建议的措施,以降低 TTvCJD 的风险。

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