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变异型克雅氏病。18年的研究与监测。

Variant CJD. 18 years of research and surveillance.

作者信息

Diack Abigail B, Head Mark W, McCutcheon Sandra, Boyle Aileen, Knight Richard, Ironside James W, Manson Jean C, Will Robert G

机构信息

a The Roslin Institute and R(D)SVS ; University of Edinburgh; Easter Bush ; Midlothian , Scotland , UK.

出版信息

Prion. 2014;8(4):286-95. doi: 10.4161/pri.29237. Epub 2014 Nov 1.

Abstract

It is now 18 years since the first identification of a case of vCJD in the UK. Since that time, there has been much speculation over how vCJD might impact human health. To date there have been 177 case reports in the UK and a further 51 cases worldwide in 11 different countries. Since establishing that BSE and vCJD are of the same strain of agent, we have also shown that there is broad similarity between UK and non-UK vCJD cases on first passage to mice. Transgenic mouse studies have indicated that all codon 129 genotypes are susceptible to vCJD and that genotype may influence whether disease appears in a clinical or asymptomatic form, supported by the appearance of the first case of potential asymptomatic vCJD infection in a PRNP 129MV patient. Following evidence of blood transfusion as a route of transmission, we have ascertained that all blood components and leucoreduced blood in a sheep model of vCJD have the ability to transmit disease. Importantly, we recently established that a PRNP 129MV patient blood recipient with an asymptomatic infection and limited PrP(Sc) deposition in the spleen could readily transmit disease into mice, demonstrating the potential for peripheral infection in the absence of clinical disease. This, along with the recent appendix survey which identified 16 positive appendices in a study of 32,441 cases, underlines the importance of continued CJD surveillance and maintaining control measures already in place to protect human health.

摘要

自英国首次确认首例变异型克雅氏病(vCJD)病例以来,已经过去了18年。从那时起,人们对vCJD如何影响人类健康进行了诸多猜测。迄今为止,英国已有177例病例报告,在全球11个不同国家又有51例病例。自从确定牛海绵状脑病(BSE)和vCJD是同一病原体毒株以来,我们还表明,英国和非英国的vCJD病例在首次接种到小鼠体内时具有广泛的相似性。转基因小鼠研究表明,所有密码子129基因型都易患vCJD,而且基因型可能会影响疾病是以临床形式还是无症状形式出现,PRNP 129MV患者中首例潜在无症状vCJD感染的出现就支持了这一点。在有证据表明输血是一种传播途径之后,我们已经确定,在vCJD的绵羊模型中,所有血液成分和白细胞滤除血液都有传播疾病的能力。重要的是,我们最近确定,一名PRNP 129MV患者血液接受者虽无症状感染且脾脏中PrP(Sc)沉积有限,但仍能轻易地将疾病传播给小鼠,这表明在没有临床疾病的情况下存在外周感染的可能性。这一点,连同最近的阑尾调查(在一项对32441例病例的研究中发现16份阳性阑尾),凸显了持续进行克雅氏病监测以及维持现有控制措施以保护人类健康的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582a/4601215/03708e1b014c/kprn-08-04-971581-g001.jpg

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