Evidence map›Paper›PMID 32577675›Full record

ArticlemedRxiv : the preprint server for health sciences2020

Serological Assays Estimate Highly Variable SARS-CoV-2 Neutralizing Antibody Activity in Recovered COVID19 Patients.

Larry L Luchsinger, Brett Ransegnola, Daniel Jin, Frauke Muecksch, Yiska Weisblum, Weili Bao, Parakkal Jovvian George, Marilis Rodriguez, Nancy Tricoche, Fabian Schmidt and 10 more

Abstract 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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Larry L LuchsingerLaboratory of Stem Cell Regenerative Research, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Brett RansegnolaLaboratory of Stem Cell Regenerative Research, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Daniel JinLaboratory of Stem Cell Regenerative Research, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Frauke MueckschLaboratory of Retrovirology, The Rockefeller University, New York, NY 10065, USA.
Yiska WeisblumLaboratory of Retrovirology, The Rockefeller University, New York, NY 10065, USA.
Weili BaoLaboratory of Complement Biology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Parakkal Jovvian GeorgeLaboratory of Molecular Parasitology Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Marilis RodriguezLaboratory of Blood-Borne Parasites, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Nancy TricocheLaboratory of Molecular Parasitology Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Fabian SchmidtLaboratory of Retrovirology, The Rockefeller University, New York, NY 10065, USA.
Chengjie GaoLaboratory of Membrane Biology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Shabnam JawaharLaboratory of Molecular Parasitology Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Mouli PalLaboratory of Complement Biology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Emily SchnallLaboratory of Molecular Parasitology Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Huan ZhangLaboratory of Membrane Biology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Donna StraussNew York Blood Center Enterprises, New York, NY 10065, USA.
Karina YazdanbakhshLaboratory of Complement Biology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Christopher D HillyerLaboratory of Stem Cell Regenerative Research, Lindsley F. Kimball Research Institute, New York Blood Center, New York, NY 10065, USA.
Paul D BieniaszLaboratory of Retrovirology, The Rockefeller University, New York, NY 10065, USA.
Theodora HatziioannouLaboratory of Retrovirology, The Rockefeller University, New York, NY 10065, USA.

Funding

Overcoming Host Restriction Factors to Develop Better Animal Models for HIV/AIDS.R01AI078788 · NIAID · ROCKEFELLER UNIVERSITY · PI HATZIIOANNOU, THEODORA · 2008 to 2021
$9.3M
Discovery and Mechanism of Antiretroviral FactorsR37AI064003 · NIAID · ROCKEFELLER UNIVERSITY · PI BIENIASZ, PAUL D. · 2011 to 2020
$4.9M
NIAID NIH HHS R01 AI078788NIAID NIH HHS R37 AI064003
6 · The paper itself

Abstract

The development of neutralizing antibodies (nAb) against SARS-CoV-2, following infection or vaccination, is likely to be critical for the development of sufficient population immunity to drive cessation of the COVID19 pandemic. A large number of serologic tests, platforms and methodologies are being employed to determine seroprevalence in populations to select convalescent plasmas for therapeutic trials, and to guide policies about reopening. However, tests have substantial variability in sensitivity and specificity, and their ability to quantitatively predict levels of nAb is unknown. We collected 370 unique donors enrolled in the New York Blood Center Convalescent Plasma Program between April and May of 2020. We measured levels of antibodies in convalescent plasma using commercially available SARS-CoV- 2 detection tests and in-house ELISA assays and correlated serological measurements with nAb activity measured using pseudotyped virus particles, which offer the most informative assessment of antiviral activity of patient sera against viral infection. Our data show that a large proportion of convalescent plasma samples have modest antibody levels and that commercially available tests have varying degrees of accuracy in predicting nAb activity. We found the Ortho Anti-SARS-CoV-2 Total Ig and IgG high throughput serological assays (HTSAs), as well as the Abbott SARS-CoV-2 IgG assay, quantify levels of antibodies that strongly correlate with nAb assays and are consistent with gold-standard ELISA assay results. These findings provide immediate clinical relevance to serology results that can be equated to nAb activity and could serve as a valuable 'roadmap' to guide the choice and interpretation of serological tests for SARS-CoV-2.

Identifiers

PMID32577675
PMCPMC7302251

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.