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现在,使用实时 QUIC 检测法可以早期检测遗传型人类朊病毒病中的异常朊病毒蛋白。

Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay.

机构信息

Department of Molecular Microbiology and Immunology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

PLoS One. 2013;8(1):e54915. doi: 10.1371/journal.pone.0054915. Epub 2013 Jan 25.

Abstract

INTRODUCTION

The definitive diagnosis of genetic prion diseases (gPrD) requires pathological confirmation. To date, diagnosis has relied upon the finding of the biomarkers 14-3-3 protein and total tau (t-tau) protein in the cerebrospinal fluid (CSF), but many researchers have reported that these markers are not sufficiently elevated in gPrD, especially in Gerstmann-Sträussler-Scheinker syndrome (GSS). We recently developed a new in vitro amplification technology, designated "real-time quaking-induced conversion (RT-QUIC)", to detect the abnormal form of prion protein in CSF from sporadic Creutzfeldt-Jakob disease (sCJD) patients. In the present study, we aimed to investigate the presence of biomarkers and evaluate RT-QUIC assay in patients with gPrD, as the utility of RT-QUIC as a diagnostic tool in gPrD has yet to be determined.

METHOD/PRINCIPAL FINDINGS: 56 CSF samples were obtained from gPrD patients, including 20 cases of GSS with P102L mutation, 12 cases of fatal familial insomnia (FFI; D178N), and 24 cases of genetic CJD (gCJD), comprising 22 cases with E200K mutation and 2 with V203I mutation. We subjected all CSF samples to RT-QUIC assay, analyzed 14-3-3 protein by Western blotting, and measured t-tau protein using an ELISA kit. The detection sensitivities of RT-QUIC were as follows: GSS (78%), FFI (100%), gCJD E200K (87%), and gCJD V203I (100%). On the other hand the detection sensitivities of biomarkers were considerably lower: GSS (11%), FFI (0%), gCJD E200K (73%), and gCJD V203I (67%). Thus, RT-QUIC had a much higher detection sensitivity compared with testing for biomarkers, especially in patients with GSS and FFI.

CONCLUSION/SIGNIFICANCE: RT-QUIC assay is more sensitive than testing for biomarkers in gPrD patients. RT-QUIC method would thus be useful as a diagnostic tool when the patient or the patient's family does not agree to genetic testing, or to confirm the diagnosis in the presence of a positive result for genetic testing.

摘要

简介

遗传性朊病毒病(gPrD)的明确诊断需要病理学确认。迄今为止,诊断依赖于在脑脊液(CSF)中发现生物标志物 14-3-3 蛋白和总 tau(t-tau)蛋白,但许多研究人员报告说,这些标志物在 gPrD 中升高不充分,尤其是在 Gerstmann-Sträussler-Scheinker 综合征(GSS)中。我们最近开发了一种新的体外扩增技术,称为“实时震颤诱导转换(RT-QUIC)”,用于检测散发性克雅氏病(sCJD)患者 CSF 中的异常形式朊病毒蛋白。在本研究中,我们旨在研究 gPrD 患者中生物标志物的存在,并评估 RT-QUIC 检测,因为 RT-QUIC 作为 gPrD 的诊断工具的实用性尚未确定。

方法/主要发现:从 gPrD 患者中获得了 56 份 CSF 样本,包括 20 例 P102L 突变的 GSS 病例、12 例致命性家族性失眠症(FFI;D178N)病例和 24 例遗传 CJD(gCJD)病例,包括 22 例 E200K 突变病例和 2 例 V203I 突变病例。我们对所有 CSF 样本进行了 RT-QUIC 检测,通过 Western blot 分析 14-3-3 蛋白,并使用 ELISA 试剂盒测量 t-tau 蛋白。RT-QUIC 的检测灵敏度如下:GSS(78%)、FFI(100%)、gCJD E200K(87%)和 gCJD V203I(100%)。另一方面,生物标志物的检测灵敏度要低得多:GSS(11%)、FFI(0%)、gCJD E200K(73%)和 gCJD V203I(67%)。因此,与生物标志物检测相比,RT-QUIC 具有更高的检测灵敏度,尤其是在 GSS 和 FFI 患者中。

结论/意义:在 gPrD 患者中,RT-QUIC 检测比生物标志物检测更敏感。因此,当患者或患者家属不同意进行基因检测,或在基因检测结果阳性时需要确认诊断时,RT-QUIC 方法将成为一种有用的诊断工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5153/3556051/80a4e157ab52/pone.0054915.g001.jpg

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