EFS-PyMed (Etablissement Français du Sang de Pyrénées Méditerranée), R&D TransDiag, Sécurité Transfusionnelle et Innovation Diagnostique, Montpellier, France.
PLoS One. 2013 Jul 24;8(7):e69632. doi: 10.1371/journal.pone.0069632. Print 2013.
Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative infectious disorder, characterized by a prominent accumulation of pathological isoforms of the prion protein (PrP(TSE)) in the brain and lymphoid tissues. Since the publication in the United Kingdom of four apparent vCJD cases following transfusion of red blood cells and one apparent case following treatment with factor VIII, the presence of vCJD infectivity in the blood seems highly probable. For effective blood testing of vCJD individuals in the preclinical or clinical phase of infection, it is considered necessary that assays detect PrP(TSE) concentrations in the femtomolar range.
METHODOLOGY/PRINCIPAL FINDINGS: We have developed a three-step assay that firstly captures PrP(TSE) from infected blood using a plasminogen-coated magnetic-nanobead method prior to its serial amplification via protein misfolding cyclic amplification (PMCA) and specific PrP(TSE) detection by western blot. We achieved a PrP(TSE) capture yield of 95% from scrapie-infected material. We demonstrated the possibility of detecting PrP(TSE) in white blood cells, in buffy coat and in plasma isolated from the blood of scrapie-infected sheep collected at the pre-clinical stage of the disease. The test also allowed the detection of PrP(TSE) in human plasma spiked with a 10(-8) dilution of vCJD-infected brain homogenate corresponding to the level of sensitivity (femtogram) required for the detection of the PrP(TSE) in asymptomatic carriers. The 100% specificity of the test was revealed using a blinded panel comprising 96 human plasma samples.
CONCLUSION/SIGNIFICANCE: We have developed a sensitive and specific amplification assay allowing the detection of PrP(TSE) in the plasma and buffy coat fractions of blood collected at the pre-clinical phase of the disease. This assay represents a good candidate as a confirmatory assay for the presence of PrP(TSE) in blood of patients displaying positivity in large scale screening tests.
变异型克雅氏病(vCJD)是一种神经退行性传染病,其特征是大脑和淋巴组织中病理性朊病毒蛋白(PrP(TSE))的明显积累。自英国发表了四起输血后明显的 vCJD 病例和一起因子 VIII 治疗后的明显病例以来,血液中存在 vCJD 感染性似乎极有可能。为了在感染的临床前或临床阶段有效检测 vCJD 个体,认为有必要检测检测方法能够检测到纳摩尔级别的 PrP(TSE)浓度。
方法/主要发现:我们开发了一种三步检测法,首先使用纤溶酶原涂层的磁性纳米珠方法从感染的血液中捕获 PrP(TSE),然后通过蛋白错误折叠循环扩增(PMCA)进行连续扩增,最后通过 Western blot 特异性检测 PrP(TSE)。我们从瘙痒病感染材料中获得了 95%的 PrP(TSE)捕获产量。我们证明了在疾病临床前阶段从感染瘙痒病的绵羊血液中分离的白细胞、血白细胞层和血浆中检测到 PrP(TSE)的可能性。该检测还允许在人血浆中检测到用 vCJD 感染性脑匀浆 10(-8)稀释液(对应于无症状携带者中 PrP(TSE)检测所需的灵敏度(飞摩尔))进行的 PrP(TSE)检测。使用包括 96 个人类血浆样本的盲法面板揭示了该检测的 100%特异性。
结论/意义:我们开发了一种敏感和特异的扩增检测法,允许在疾病临床前阶段采集的血液血浆和白细胞层部分中检测到 PrP(TSE)。该检测法有望成为在大规模筛查试验中呈阳性的患者血液中存在 PrP(TSE)的确认检测法。