Evidence map›Paper›PMID 33842901›Full record

ArticleCell reports. Medicine2021

Rapid decline of neutralizing antibodies is associated with decay of IgM in adults recovered from mild COVID-19.

Whitney E Harrington, Olesya Trakhimets, Daniela V Andrade, Nicholas Dambrauskas, Andrew Raappana, Yonghou Jiang, John Houck, William Selman, Ashton Yang, Vladimir Vigdorovich and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% of its field
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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

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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

20 authors at 2 institutions in 1 country.

Whitney E HarringtonCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Olesya TrakhimetsCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Daniela V AndradeCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Nicholas DambrauskasCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Andrew RaappanaCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Yonghou JiangCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
John HouckCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
William SelmanCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Ashton YangCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Vladimir VigdorovichCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Winnie YeungCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Micaela HaglundCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Jackson WallnerCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Alyssa OldroydCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Samantha HardyCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Samuel W A StewartCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Ana GervassiCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Wes Van VoorhisCenter for Emerging and Re-emerging Infectious Diseases, University of Washington, Seattle, WA 98109, USA.
Lisa FrenkelCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
D Noah SatherCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Infectious Disease Research Institute · USUniversity of Washington · US

Funding

Kinetics, evolution, and effector function of Fc repertoires during vaccination with native-like Env trimersR01AI140951 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI SATHER, D. NOAH · 2019 to 2023
$4.4M
The Effect of Maternal Cells on Infant ImmunityK08AI135072 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI HARRINGTON, WHITNEY ELIZABETH · 2018 to 2022
$854k
NIAID NIH HHS K08 AI135072NIAID NIH HHS R01 AI140951
6 · The paper itself

Abstract

The fate of protective immunity following mild severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) infection remains ill defined. Here, we characterize antibody responses in a cohort of participants recovered from mild SARS-CoV-2 infection with follow-up to 6 months. We measure immunoglobulin A (IgA), IgM, and IgG binding and avidity to viral antigens and assess neutralizing antibody responses over time. Furthermore, we correlate the effect of fever, gender, age, and time since symptom onset with antibody responses. We observe that total anti-S trimer, anti-receptor-binding domain (RBD), and anti-nucleocapsid protein (NP) IgG are relatively stable over 6 months of follow-up, that anti-S and anti-RBD avidity increases over time, and that fever is associated with higher levels of antibodies. However, neutralizing antibody responses rapidly decay and are strongly associated with declines in IgM levels. Thus, while total antibody against SARS-CoV-2 may persist, functional antibody, particularly IgM, is rapidly lost. These observations have implications for the duration of protective immunity following mild SARS-CoV-2 infection.

Indexed as

AdultAgedAntibodies, NeutralizingCOVID-19FemaleFeverHumansImmunoglobulin GImmunoglobulin MMaleMiddle AgedNeutralization TestsNucleocapsid ProteinsProtein DomainsProtein MultimerizationSARS-CoV-2Antibodies, NeutralizingImmunoglobulin GImmunoglobulin MNucleocapsid ProteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibody avidityCOVID-19IgGIgMmild infectionneutralizing antibodiesSARS-CoV-2

Identifiers

PMID33842901
PMCPMC8020863
OpenAlexW3141930699

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.