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线性表位在肽酶联免疫吸附试验中的诊断性能评估。

Evaluation of the Diagnostic Performance of Linear Epitopes in a Peptide Enzyme-Linked Immunosorbent Assay.

机构信息

Janssen Diagnostics, Janssen R&D, Beerse, Belgium.

Kumasi Centre for Collaborative Research into Tropical medicine, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

出版信息

Am J Trop Med Hyg. 2018 Mar;98(3):779-785. doi: 10.4269/ajtmh.17-0756. Epub 2018 Jan 4.

Abstract

Diagnostic tools for the detection of infection with are presently limited to microfilaria detection in skin biopsies and serological assessment using the Ov16 immunoglobulin G4 (IgG4) rapid test, both of which have limited sensitivity. We have investigated the diagnostic performance of a peptide enzyme-linked immunosorbent assay (ELISA) based on immunodominant linear epitopes previously discovered. Peptides that were used in these assays were designated motif peptides (OvMP): OvMP-1 (VSV-EPVTTQET-VSV), OvMP-2 (VSV-KDGEDK-VSV), OvMP-3 (VSV-QTSNLD-VSV), and the combination of the latter two, OvMP-23 (VSV-KDGEDK-VSV-QTSNLD-VSV). Sensitivity ( infection), specificity (non-helminth infections), and cross-reactivity (helminth infections) were determined using several panels of clinical plasma isolates. OvMP-1 was found to be very sensitive (100%) and specific (98.7%), but showed substantial cross-reactivity with other helminths. Of the other peptides, OvMP-23 was the most promising peptide with a sensitivity of 92.7%, a specificity of 100%, and a cross-reactivity of 6%. It was also demonstrated that these peptides were immunoreactive to IgG but not IgG4, and there is no correlation with the Ov16 IgG4 status, making them promising candidates to complement this already available test. Combination of the Ov16 IgG4 rapid test and OvMP-23 peptide ELISA led to a sensitivity of 97.3% for the detection of infection, without compromising specificity and with minimal impact on cross-reactivity. The available results open the opportunity for a "" discussion for improved epidemiological mapping.

摘要

目前,用于检测感染的诊断工具仅限于皮肤活检中的微丝蚴检测和使用 Ov16 免疫球蛋白 G4(IgG4)快速检测进行的血清学评估,这两种方法的敏感性都有限。我们研究了先前发现的基于免疫显性线性表位的肽酶联免疫吸附试验(ELISA)的诊断性能。用于这些检测的肽被指定为 OvMP 肽:OvMP-1(VSV-EPVTTQET-VSV)、OvMP-2(VSV-KDGEDK-VSV)、OvMP-3(VSV-QTSNLD-VSV)以及后两者的组合 OvMP-23(VSV-KDGEDK-VSV-QTSNLD-VSV)。使用几个人群临床血浆分离物面板确定了敏感性( 感染)、特异性(非寄生虫感染)和交叉反应性(寄生虫感染)。发现 OvMP-1 非常敏感(100%)和特异性(98.7%),但与其他寄生虫有很大的交叉反应。在其他肽中,OvMP-23 是最有希望的肽,其敏感性为 92.7%,特异性为 100%,交叉反应性为 6%。还证明这些肽对 IgG 有免疫反应性,但对 IgG4 没有免疫反应性,并且与 Ov16 IgG4 状态没有相关性,这使它们成为补充这种现有检测方法的有希望的候选物。将 Ov16 IgG4 快速检测与 OvMP-23 肽 ELISA 结合使用,可将 感染的检测敏感性提高到 97.3%,而特异性和交叉反应性不受影响。现有结果为进行“ ”讨论以改善 流行病学绘图提供了机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c02b/5930915/f2d7d8e3c096/tpmd170756f1.jpg

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