Evidence map›Paper›PMID 34268524›Full record

ArticlemedRxiv : the preprint server for health sciences2021

Longitudinal variation in SARS-CoV-2 antibody levels and emergence of viral variants: implications for the ability of serological assays to predict immunity.

Frauke Muecksch, Helen Wise, Kate Templeton, Becky Batchelor, Maria Squires, Kirsty McCance, Lisa Jarvis, Kristen Malloy, Elizabeth Furrie, Claire Richardson and 9 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2021. 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, 16 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 3 countries.

Frauke Muecksch *Laboratory of Retrovirology, The Rockefeller University, 1230 York Avenue, New York NY 10065.
Helen Wise *Royal Infirmary of Edinburgh, NHS Lothian, 51 Little France Crescent, Edinburgh EH16 4SA.
Kate TempletonRoyal Infirmary of Edinburgh, NHS Lothian, 51 Little France Crescent, Edinburgh EH16 4SA.
Becky BatchelorWestern General Hospital, Crewe Road South, Edinburgh, EH4 2XU.
Maria SquiresRoyal Infirmary of Edinburgh, NHS Lothian, 51 Little France Crescent, Edinburgh EH16 4SA.
Kirsty McCanceRoyal Infirmary of Edinburgh, NHS Lothian, 51 Little France Crescent, Edinburgh EH16 4SA.
Lisa JarvisSNBTS Microbiology Reference Laboratory, The Jack Copland Centre, 52 Research Avenue North, Heriot Watt Research Park, Edinburgh, EH14 4AP.
Kristen MalloySNBTS Microbiology Reference Laboratory, The Jack Copland Centre, 52 Research Avenue North, Heriot Watt Research Park, Edinburgh, EH14 4AP.
Elizabeth FurrieNinewells Hospital and Medical School, NHS Tayside, Dundee, DD1 9SY.
Claire RichardsonUniversity Hospital Monklands, NHS Lanarkshire, Airdrie, ML6 0JS.
Jacqueline MacGuireUniversity Hospital Monklands, NHS Lanarkshire, Airdrie, ML6 0JS.
Ian GodberQueen Elizabeth University Hospital, Govan Road, Glasgow, G51 4TF.
Alana BurnsQueen Elizabeth University Hospital, Govan Road, Glasgow, G51 4TF.
Sally MavinScottish Microbiology Reference Laboratory, NHS Highland, Inverness, IV2 3UJ.
Fengwen ZhangLaboratory of Retrovirology, The Rockefeller University, 1230 York Avenue, New York NY 10065.
Fabian SchmidtLaboratory of Retrovirology, The Rockefeller University, 1230 York Avenue, New York NY 10065.
Paul BieniaszLaboratory of Retrovirology, The Rockefeller University, 1230 York Avenue, New York NY 10065.
Sara JenksRoyal Infirmary of Edinburgh, NHS Lothian, 51 Little France Crescent, Edinburgh EH16 4SA.
Theodora HatziioannouLaboratory of Retrovirology, The Rockefeller University, 1230 York Avenue, New York NY 10065.
Rockefeller University · USHeriot-Watt University · GBNHS Lanarkshire · GBQueen Elizabeth University Hospital · GBHoward Hughes Medical Institute · USNHS Highland · GBNHS Tayside · GBWestern General Hospital · GB

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
RNA Protein interactions in HIV-1 replicationR01AI050111 · NIAID · ROCKEFELLER UNIVERSITY · PI BIENIASZ, PAUL D. · 2001 to 2021
$7.9M
NIAID NIH HHS R01 AI050111NIAID NIH HHS R01 AI078788
6 · The paper itself

Abstract

backgroundSerological assays are being deployed to monitor antibody responses in SARS-CoV-2 convalescents and vaccine recipients. There is a need to determine whether such assays can predict immunity, as antibody levels wane and viral variants emerge.

methodsWe measured antibodies in a cohort of SARS-CoV-2 infected patients using several high-throughput serological tests and functional neutralization assays. The effects of time and spike protein sequence variation on the performance and predictive value of the various assays was assessed.

findingsNeutralizing antibody titers decreased over the first few months post-infection but stabilized thereafter, at about 30% of the level observed shortly after infection. Serological assays commonly used to measure antibodies against SARS-CoV-2 displayed a range of sensitivities that declined to varying extents over time. Quantitative measurements generated by serological assays based on the spike protein were better at predicting neutralizing antibody titers than assays based on nucleocapsid, but performance was variable and manufacturer positivity thresholds were not able to predict the presence or absence of detectable neutralizing activity. Even though there was some deterioration in correlation between serological measurements and functional neutralization activity, some assays maintained an ability to predict neutralizing titers, even against variants of concern.

interpretationThe ability of high throughput serological assays to predict neutralizing antibody titers is likely crucial for evaluation of immunity at the population scale. These data will facilitate the selection of the most suitable assays as surrogates of functional neutralizing activity and suggest that such measurements may have utility in clinical practice.

Identifiers

PMID34268524
PMCPMC8282113
OpenAlexW3182155919

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.