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沉默抗体开始说话:通过将标签分两步掺入免疫复合物增强侧向流动血清诊断。

Silent Antibodies Start Talking: Enhanced Lateral Flow Serodiagnosis with Two-Stage Incorporation of Labels into Immune Complexes.

机构信息

A.N. Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, Leninsky Prospect 33, 119071 Moscow, Russia.

State Key Laboratory of Membrane Biology, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing 100084, China.

出版信息

Biosensors (Basel). 2022 Jun 21;12(7):434. doi: 10.3390/bios12070434.

Abstract

The presence of pathogen-specific antibodies in the blood is widely controlled by a serodiagnostic technique based on the lateral flow immunoassay (LFIA). However, its common one-stage format with an antigen immobilized in the binding zone of a test strip and a nanodispersed label conjugated with immunoglobulin-binding proteins is associated with risks of very low analytical signals. In this study, the first stage of the immunochromatographic serodiagnosis was carried out in its traditional format using a conjugate of gold nanoparticles with staphylococcal immunoglobulin-binding protein A and an antigen immobilized on a working membrane. At the second stage, a labeled immunoglobulin-binding protein was added, which enhanced the coloration of the bound immune complexes. The use of two separated steps, binding of specific antibodies, and further coloration of the formed complexes, allowed for a significant reduction of the influence of non-specific immunoglobulins on the assay results. The proposed approach was applied for the serodiagnosis using a recombinant RBD protein of SARS-CoV-2. As a result, an increase in the intensity of test zone coloration by more than two orders of magnitude was demonstrated, which enabled the significant reduction of false-negative results. The diagnostic sensitivity of the LFIA was 62.5% for the common format and 100% for the enhanced format. Moreover, the diagnostic specificity of both variants was 100%.

摘要

血液中病原体特异性抗体的存在广泛受到基于侧向流动免疫分析(LFIA)的血清诊断技术的控制。然而,其常见的单阶段格式,即将抗原固定在测试条的结合区,而纳米分散的标签与免疫球蛋白结合蛋白结合,存在分析信号非常低的风险。在这项研究中,免疫层析血清诊断的第一阶段采用金纳米粒子与葡萄球菌免疫球蛋白结合蛋白 A 的缀合物和固定在工作膜上的抗原进行传统格式。在第二阶段,添加了标记的免疫球蛋白结合蛋白,这增强了结合免疫复合物的着色。使用两个分开的步骤,即特异性抗体的结合和随后形成的复合物的着色,大大降低了非特异性免疫球蛋白对检测结果的影响。该方法用于使用 SARS-CoV-2 的重组 RBD 蛋白进行血清诊断。结果,测试区着色强度增加了两个数量级以上,从而显著降低了假阴性结果的数量。LFIA 的诊断灵敏度对于常见格式为 62.5%,对于增强格式为 100%。此外,两种变体的诊断特异性均为 100%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa6c/9313186/c4fd46580175/biosensors-12-00434-g001.jpg

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