Evidence map›Paper›PMID 33515984›Full record

ArticleBiosensors & bioelectronics2021

Testing-on-a-probe biosensors reveal association of early SARS-CoV-2 total antibodies and surrogate neutralizing antibodies with mortality in COVID-19 patients.

He S Yang, Sabrina E Racine-Brzostek, Mohsen Karbaschi, Jim Yee, Alicia Dillard, Peter A D Steel, William T Lee, Kathleen A McDonough, Yuqing Qiu, Thomas J Ketas and 15 more

Open access · greenAbstract readValidation Study
In one paragraph

Article in Biosensors & bioelectronics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 5 institutions in 1 country.

He S YangDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
Sabrina E Racine-BrzostekDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
Mohsen KarbaschiET HealthCare, Palo Alto, CA, USA.
Jim YeeNewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
Alicia DillardDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
Peter A D SteelNewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA; Department of Emergency Medicine, Weill Cornell Medical Center, New York, NY, USA.
William T LeeDiagnostic Immunology Laboratory, Wadsworth Center, New York State Department of Health, Albany, NY, USA.
Kathleen A McDonoughDiagnostic Immunology Laboratory, Wadsworth Center, New York State Department of Health, Albany, NY, USA.
Yuqing QiuDepartment of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
Thomas J KetasDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY, USA.
Erik FrancomanoDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY, USA.
P J KlasseDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY, USA.
Layla HatemDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
Lars WestbladeDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Heng WuET HealthCare, Palo Alto, CA, USA.
Haode ChenET HealthCare, Palo Alto, CA, USA.
Robert ZukET HealthCare, Palo Alto, CA, USA.
Hong TanET HealthCare, Palo Alto, CA, USA.
Roxanne C GirardinDiagnostic Immunology Laboratory, Wadsworth Center, New York State Department of Health, Albany, NY, USA.
Alan P DupuisDiagnostic Immunology Laboratory, Wadsworth Center, New York State Department of Health, Albany, NY, USA.
Anne F PayneDiagnostic Immunology Laboratory, Wadsworth Center, New York State Department of Health, Albany, NY, USA.
John P MooreDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, NY, USA.
Melissa M CushingDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
Amy ChadburnDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA.
Zhen ZhaoDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA; NewYork-Presbyterian Hospital/Weill Cornell Medical Campus, New York, NY, USA. Electronic address: zhz9010@med.cornell.edu.
Cornell University · USNew York Hospital Queens · USNew York State Department of Health · USWeill Cornell Medicine · USWadsworth Center · US

Funding

Structural studies of native-like SOSIP trimersP01AI110657 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MOORE, JOHN P · 2015 to 2024
$35.4M
Neutralization of Primate Immunodeficiency VirusesR01AI036082 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI JOHN P MOORE · 1994 to 2026
$4.3M
NIAID NIH HHS P01 AI110657NIAID NIH HHS R01 AI036082
6 · The paper itself

Abstract

The association of mortality with the early humoral response to SARS-CoV-2 infection within the first few days after onset of symptoms (DAOS) has not been thoroughly investigated partly due to a lack of sufficiently sensitive antibody testing methods. Here we report two sensitive and automated testing-on-a-probe (TOP) biosensor assays for SARS-CoV-2 viral specific total antibodies (TAb) and surrogate neutralizing antibodies (SNAb), which are suitable for clinical use. The TOP assays employ an RBD-coated quartz probe using a Cy5-Streptavidin-polysacharide conjugate to improve sensitivity and minimize interference. Disposable cartridges containing pre-dispensed reagents require no liquid manipulation or fluidics during testing. The TOP-TAb assay exhibited higher sensitivity in the 0-7 DAOS window than a widely used FDA-EUA assay. The rapid and automated TOP-SNAb correlated well with two well-established SARS-CoV-2 virus neutralization tests. The clinical utility of the TOP assays was demonstrated by evaluating early antibody responses in 120 SARS-CoV-2 RT-PCR positive adult hospitalized patients. Higher TAb and SNAb positivity rates and more robust antibody responses at patient's initial hospital presentation were seen in inpatients who survived COVID-19 than those who died in the hospital. Survival analysis using the Cox Proportional Hazards Model showed that patients who had negative TAb and/or SNAb at initial hospital presentation were at a higher risk of in-hospital mortality. Furthermore, TAb and SNAb levels at presentation were inversely associated with SARS-CoV-2 viral load based on concurrent RT-PCR testing. Overall, the sensitive and automated TAb and SNAb assays allow the detection of early SARS-CoV-2 antibodies which associate with mortality.

Indexed as

AdultAgedAged, 80 and overAntibodies, NeutralizingAntibodies, ViralBiosensing TechniquesCohort StudiesCOVID-19COVID-19 Nucleic Acid TestingCOVID-19 Serological TestingEquipment DesignFemaleHumansMaleMiddle AgedNeutralization TestsAntibodies, NeutralizingAntibodies, ViralAcute humoral responseCoronavirus Disease-2019 (COVID-19)MortalityNeutralizing antibodySARS-CoV-2 antibodyTesting-on-a-probe biosensors

Identifiers

PMID33515984
PMCPMC7816890
OpenAlexW3124562652

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.