Evidence map›Paper›PMID 33269345›Full record

ArticleResearch square2020

A betacoronavirus multiplex microsphere immunoassay detects early SARS-CoV-2 seroconversion and antibody cross reactions.

Eric Laing, Spencer Sterling, Stephanie Richard, Nusrat Epsi, Shreshta Phogat, Emily Samuels, Lianying Yan, Nicole Moreno, Christian Coles, Matthew Drew and 15 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Understanding COVID-19-associated coagulopathy.Nature reviews. Immunology · 2022
    Review
  2. Article
  3. Review
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

25 authors at 5 institutions in 2 countries.

Eric LaingUniformed Services University.
Spencer SterlingUniformed Services University of the Health Sciences.
Stephanie RichardUniformed Services University/Henry M. Jackson Foundation.
Nusrat EpsiUniformed Services University/Henry M. Jackson Foundation.
Shreshta PhogatUniformed Services University/Henry M. Jackson Foundation.
Emily SamuelsUniformed Services University/Henry M. Jackson Foundation.ORCID 0000-0002-5139-7808
Lianying YanUniformed Services University of the Health Sciences.
Nicole MorenoUniformed Services University/Henry M. Jackson Foundation.
Christian ColesUniformed Services University/Henry M. Jackson Foundation.
Matthew DrewFrederick National Laboratory for Cancer Research.
Jennifer MehalkoFrederick National Laboratory for Cancer Research.
Caroline EnglishUniformed Services University/Henry M. Jackson Foundation.
Scott MerrittUniformed Services University/Henry M. Jackson Foundation/Brooke Army Medical Center.
Katrin MendeUniformed Services University/Henry M. Jackson Foundation/Brooke Army Medical Center.
Kevin ChungUniformed Services University.
G CliftonBrooke Army Medical Center.
Vincent MunsterNational Institute of Allergy and Infectious Diseases.ORCID 0000-0002-2288-3196
Emmie de WitNational Institute of Allergy and Infectious Diseases.ORCID 0000-0002-9763-7758
David TribbleUniformed Services University.
Brian AganUniformed Services University/Henry M. Jackson Foundation.
Dominic EspositoFrederick National Laboratory for Cancer Research.ORCID 0000-0002-9987-1687
Charlotte LanteriUniformed Services University.
Edward MitreUniformed Services University.
Timothy BurgessUniformed Services University.
Chritopher BroderUniformed Services University of the Health Sciences.
Unifor · NOFrederick National Laboratory for Cancer Research · USUniformed Services University of the Health Sciences · USNational Institute of Allergy and Infectious Diseases · USBrooke Army Medical Center · US

Funding

NIAID NIH HHS Y01 AI005072
6 · The paper itself

Abstract

Sensitive and specific SARS-CoV-2 antibody assays remain critical for community and hospital-based SARS-CoV-2 surveillance. Here, we developed and applied a multiplex microsphere-based immunoassay (MMIA) for COVD-19 antibody studies that incorporates spike protein trimers of SARS-CoV-2, SARS-CoV-1, MERS-CoV, and the seasonal human betacoronaviruses, HCoV-HKU1 and HCoV-OC43, that enables measurement of off-target pre-existing cross-reactive antibodies. The MMIA performances characteristics are: 98% sensitive and 100% specific for human subject samples collected as early as 10 days from symptom onset. The MMIA permitted the simultaneous identification of SARS-CoV-2 seroconversion and the induction of SARS-CoV-2 IgG antibody cross reactions to SARS-CoV-1 and MERS-CoV. Further, synchronous increases of HCoV-OC43 IgG antibody levels was detected with SARS-CoV-2 seroconversion in a subset of subjects for whom early infection sera were available prior to their SARS-CoV-2 seroconversion, suggestive of an HCoV-OC43 memory response triggered by SARS-CoV-2 infection.

Indexed as

multiplex microsphere-based immunoassaySARS-CoV-2seroconversion

Identifiers

PMID33269345
PMCPMC7709164
OpenAlexW3107594096

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.