Evidence map›Paper›PMID 34942543›Full record

ArticleBiosensors & bioelectronics2022

Dual-detection fluorescent immunochromatographic assay for quantitative detection of SARS-CoV-2 spike RBD-ACE2 blocking neutralizing antibody.

Xuejun Duan, Yijun Shi, Xudong Zhang, Xiaoxiao Ge, Rong Fan, Jinghan Guo, Yubin Li, Guoge Li, Yaowei Ding, Rasha Alsamani Osman and 4 more

Open access · greenAbstract read
In one paragraph

Article in Biosensors & bioelectronics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 37 citations in OpenAlex.

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  15. Evaluation of a rapid semiquantitative lateral flow assay for the prediction of serum neutralizing activity against SARS-CoV-2 variants.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Xuejun DuanBeijing North Institute of Biotechnology Co., Ltd., NO. A20 Panjiamiao, Fengtai Distrct, Beijing, China. Electronic address: xzs_duanxuejun@163.com.
Yijun ShiDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China.
Xudong ZhangBeijing North Institute of Biotechnology Co., Ltd., NO. A20 Panjiamiao, Fengtai Distrct, Beijing, China.
Xiaoxiao GeBeijing Institute of Brain Disorders, Capital Medical Univerity, Beijing, China.
Rong FanBeijing North Institute of Biotechnology Co., Ltd., NO. A20 Panjiamiao, Fengtai Distrct, Beijing, China.
Jinghan GuoBeijing North Institute of Biotechnology Co., Ltd., NO. A20 Panjiamiao, Fengtai Distrct, Beijing, China.
Yubin LiBeijing North Institute of Biotechnology Co., Ltd., NO. A20 Panjiamiao, Fengtai Distrct, Beijing, China.
Guoge LiDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China.
Yaowei DingDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China.
Rasha Alsamani OsmanDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China.
Wencan JiangDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China.
Jialu SunDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China.
Xin LuanDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China.
Guojun ZhangDepartment of Clinical Diagnosis, Laboratory of Beijing Tiantan Hospital, Capital Medical University, Beijing, China; NMPA Key Laboratory for Quality Control of In Vitro Diagnostics, Beijing, China; Beijing Engineering Research Center of Immunological Reagents Clinical Research, Beijing, China. Electronic address: tiantanzgj@163.com.
Capital Medical University · CNNorth China Institute of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global effort against the COVID-19 pandemic dictates that routine quantitative detection of SARS-CoV-2 neutralizing antibodies is vital for assessing immunity following periodic revaccination against new viral variants. Here, we report a dual-detection fluorescent immunochromatographic assay (DFIA), with a built-in self-calibration process, that enables rapid quantitative detection of neutralizing antibodies that block binding between the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein and the angiotensin-converting enzyme 2 (ACE2). Thus, this assay is based on the inhibition of binding between ACE2 and the RBD of the SARS-CoV-2 spike protein by neutralizing antibodies, and the affinity of anti-human immunoglobulins for these neutralizing antibodies. Our self-calibrating DFIA shows improved precision and sensitivity with a wider dynamic linear range, due to the incorporation of a ratiometric algorithm of two-reverse linkage signals responding to an analyte. This was evident by the fact that no positive results (0/14) were observed in verified negative samples, while 22 positives were detected in 23 samples from verified convalescent plasma. A comparative analysis of the ability to detect neutralizing antibodies in 266 clinical serum samples including those from vaccine recipients, indicated that the overall percent agreement between DFIA and the commercial ELISA kit was 90.98%. Thus, the proposed DFIA provides a more reliable and accurate rapid test for detecting SARS-CoV-2 infections and vaccinations in the community. Therefore, the DFIA based strategy for detecting biomarkers, which uses a ratiometric algorithm based on affinity and inhibition reactions, may be applied to improve the performance of immunochromatographic assays.

Indexed as

Biosensing TechniquesCOVID-19Angiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralCOVID-19 SerotherapyHumansImmunization, PassiveImmunoassayPandemicsSARS-CoV-2Spike Glycoprotein, CoronavirusAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Dual-detectionLateral flow assayNeutralization antibodyPoint of care testingRatiometric biosensorSARS CoV-2

Identifiers

PMID34942543
PMCPMC8673933
OpenAlexW4200446885

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.