Evidence map›Paper›PMID 33173900›Full record

ArticlemedRxiv : the preprint server for health sciences2020

Multiplexed, quantitative serological profiling of COVID-19 from a drop of blood by a point-of-care test.

Jacob T Heggestad, David S Kinnamon, Lyra B Olson, Jason Liu, Garrett Kelly, Simone A Wall, Cassio M Fontes, Daniel Y Joh, Angus M Hucknall, Carl Pieper and 10 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 2 institutions in 1 country.

Jacob T HeggestadDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
David S KinnamonDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Lyra B OlsonDuke Medical Scientist Training Program, Department of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC 27710 USA.
Jason LiuDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Garrett KellyDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Simone A WallDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Cassio M FontesDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Daniel Y JohDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Angus M HucknallDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Carl PieperDepartments of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, NC 27708 USA.
Ibtehaj A NaqviDepartment of Surgery, Duke University School of Medicine, Durham, NC 27710 USA.
Lingye ChenDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, NC 27710 USA.
Loretta G QueDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, NC 27710 USA.
Thomas OguinDepartment of Medicine and Duke Human Vaccine Institute, School of Medicine, Duke University, Durham, NC 27710 USA.
Smita K NairDepartment of Surgery, Duke University School of Medicine, Durham, NC 27710 USA.
Bruce A SullengerDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Christopher W WoodsDepartment of Medicine and Duke Human Vaccine Institute, School of Medicine, Duke University, Durham, NC 27710 USA.
Gregory D SempowskiDepartment of Medicine and Duke Human Vaccine Institute, School of Medicine, Duke University, Durham, NC 27710 USA.
Bryan D KraftDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, NC 27710 USA.
Ashutosh ChilkotiDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708 USA.
Duke University · USDuke Medical Center · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI JOHN N. NORTON · 1985 to 2026
$174.8M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Regional Biocontainment Laboratory (RBL)UC6AI058607 · NIAID · DUKE UNIVERSITY · PI WILLIAMS, R SANDERS · 2003 to 2005
$16.3M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
A Fully Integrated Point-of-Care Test for EbolaR01AI150888 · NIAID · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH · 2020 to 2024
$3.4M
Point-of-care cellular and molecular pathology of breast tumors on a cell phoneR01CA248491 · NCI · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH, HWANG, E. SHELLEY · 2020 to 2024
$2.9M
Smartphone Enabled Point-of-Care Detection of Serum Markers of Liver CancerUH3CA211232 · NCI · DUKE UNIVERSITY · PI CHAO, NELSON J., CHILKOTI, ASHUTOSH · 2019 to 2021
$1.9M
Role of S-nitrosothiols in Akt1 signaling and pneumonia resolutionK08HL130557 · NHLBI · DUKE UNIVERSITY · PI KRAFT, BRYAN D. · 2017 to 2021
$591k
NCI NIH HHS P30 CA014236NCI NIH HHS R01 CA248491NCI NIH HHS UH3 CA211232NHLBI NIH HHS K08 HL130557NIAID NIH HHS R01 AI150888NIAID NIH HHS UC6 AI058607NIGMS NIH HHS T32 GM007171NIGMS NIH HHS T32 GM145449
6 · The paper itself

Abstract

Highly sensitive, specific, and point-of-care (POC) serological assays are an essential tool to manage the COVID-19 pandemic. Here, we report on a microfluidic, multiplexed POC test that can profile the antibody response against multiple SARS-CoV-2 antigens - Spike S1 (S1), Nucleocapsid (N), and the receptor binding domain (RBD) - simultaneously from a 60 microliter drop of blood, plasma, or serum. We assessed the levels of anti-SARS-CoV-2 antibodies in plasma samples from 19 individuals (at multiple time points) with COVID-19 that required admission to the intensive care unit and from 10 healthy individuals. This POC assay shows good concordance with a live virus microneutralization assay, achieved high sensitivity (100%) and specificity (100%), and successfully tracked the longitudinal evolution of the antibody response in infected individuals. We also demonstrated that we can detect a chemokine, IP-10, on the same chip, which may provide prognostic insight into patient outcomes. Because our test requires minimal user intervention and is read by a handheld detector, it can be globally deployed in the fight against COVID-19 by democratizing access to laboratory quality tests.

Identifiers

PMID33173900
PMCPMC7654894
OpenAlexW3103627439

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.