Evidence map›Paper›PMID 39470282›Full record

ArticleMicrobiology spectrum2024

Quantitating SARS-CoV-2 neutralizing antibodies from human dried blood spots.

Katherine Berman, Greta Van Slyke, Hayley Novak, Jean M Rock, Rachel Bievenue, Amanda K Damjanovic, Kate L DeRosa, Gianna Mirabile, Kara Phipps, Jessica Machowski and 9 more

Abstract read
In one paragraph

Article in Microbiology spectrum, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Katherine BermanDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Greta Van SlykeDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Hayley NovakDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Jean M RockDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Rachel BievenueDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Amanda K DamjanovicDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Kate L DeRosaDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Gianna MirabileDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Kara PhippsDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Jessica MachowskiDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Sean BialosukniaDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Roxie C GiradinDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Alan P DupuisDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Anne F PayneDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
William T LeeDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.ORCID 0000-0003-2883-0391
Kathleen A McDonoughDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.
Monica M ParkerDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.ORCID 0000-0001-7806-968X
Linda M StyerDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.ORCID 0000-0001-8137-0318
Nicholas J MantisDivision of Infectious Disease, Wadsworth Center, New York State Department of Health, Albany, New York, USA.ORCID 0000-0002-5083-8640

Funding

High-Throughput Dried Blood Spot (HT-DBS) Technologies in SARS COV-2 Serology and VaccinologyU01CA260508 · NCI · WADSWORTH CENTER · PI MANTIS, NICHOLAS J. · 2020 to 2023
$2.6M
DOC | NIST | National Institute for Innovation in Manufacturing Biopharmaceuticals (NIIMBL) COVID19-1.01HHS | NIH | National Cancer Institute (NCI) U01CA260508NCI NIH HHS U01 CA260508
6 · The paper itself

Abstract

In the earliest days of the COVID-19 pandemic, the collection of dried blood spots (DBS) enabled public health laboratories to undertake population-scale seroprevalence studies used to estimate rates of SARS-CoV-2 exposure. With SARS-CoV-2 seropositivity levels now estimated to exceed 94% in the United States, attention has turned to using DBS to assess neutralizing antibodies within cohorts of interest. With this goal in mind, we generated contrived DBS (cDBS) and whole blood-derived DBS from convalescent and vaccinated individuals and subjected DBS eluates to a battery of assays, including a SARS-CoV-2 multiplexed microsphere immunoassay (MIA), a receptor binding domain (RBD)-human ACE2 inhibition assay (iACE2), a cell-based pseudovirus neutralization assay, and real-time PCR-based surrogate neutralization assay (NAB-Sure). The DBS results were benchmarked against paired serum samples tested in a clinically validated SARS-CoV-2 plaque reduction neutralization titer (PRNT) assay. The results of an 8-plex MIA and NAB-Sure assays demonstrated highly significant correlations with PRNT values when evaluated with a panel of 86 paired serum-DBS samples. Both the MIA and NAB-Sure are adaptable to automated liquid handlers for high-throughput capacity. While neutralizing assays were limited to the ancestral SARS-CoV-2 WA1, this study nonetheless represents an important proof of concept demonstrating the potential utility of DBS as a biospecimen type for use in assessing immunity to SARS-CoV-2 at the community and population levels.IMPORTANCESARS-CoV-2 variants of concern continue to circulate globally and remain a serious health threat to large segments of the population. From a public health standpoint, identifying vulnerable communities based on immune status is critical in terms of vaccine booster recommendations. In this report, we investigated the utility of dried blood spots (DBS) as a biospecimen type from which to estimate SARS-CoV-2 neutralizing antibody titers. Using contrived and whole blood-derived DBS, we demonstrate that SARS-CoV-2 neutralizing antibodies are readily measurable in DBS eluates and correlate with plaque reduction neutralization titer (PRNT) values from paired serum samples. Moreover, several of the methods used to estimate SARS-CoV-2 neutralizing antibodies in DBS eluates are adaptable to high-throughput platforms.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCOVID-19Dried Blood Spot TestingSARS-CoV-2COVID-19 Serological TestingHumansImmunoassayNeutralization TestsAntibodies, NeutralizingAntibodies, ViralantibodyCOVID-19humanneutralizingserology

Identifiers

PMID39470282
PMCPMC11619372

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.