Evidence map›Paper›PMID 35123650›Full record

ArticleCell2022

SARS-CoV-2 breakthrough infections elicit potent, broad, and durable neutralizing antibody responses.

Alexandra C Walls, Kaitlin R Sprouse, John E Bowen, Anshu Joshi, Nicholas Franko, Mary Jane Navarro, Cameron Stewart, Elisabetta Cameroni, Matthew McCallum, Erin A Goecker and 6 more

Abstract read
In one paragraph

Article in Cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
144citing papers in PubMed, 1 pooled it
–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

144 citing papers in PubMed, 1 synthesis or guideline pooled it.

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84 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Alexandra C WallsDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA. Electronic address: acwalls@uw.edu.
Kaitlin R SprouseDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA.
John E BowenDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA.
Anshu JoshiDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA.
Nicholas FrankoDivision of Allergy and Infectious Diseases, University of Washington, Seattle, WA 98195, USA.
Mary Jane NavarroDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA.
Cameron StewartDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA.
Elisabetta CameroniHumabs Biomed SA, a Subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.
Matthew McCallumDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA.
Erin A GoeckerDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Emily J Degli-AngeliDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Jenni LogueDivision of Allergy and Infectious Diseases, University of Washington, Seattle, WA 98195, USA.
Alex GreningerDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Davide CortiHumabs Biomed SA, a Subsidiary of Vir Biotechnology, 6500 Bellinzona, Switzerland.
Helen Y ChuDivision of Allergy and Infectious Diseases, University of Washington, Seattle, WA 98195, USA.
David VeeslerDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA. Electronic address: dveesler@uw.edu.

Funding

Unraveling the bat humoral immune response against zoonotic viruses to guide the design of next-generation therapeuticsDP1AI158186 · NIAID · UNIVERSITY OF WASHINGTON · PI VEESLER, DAVID · 2020 to 2024
$5.4M
NIAID NIH HHS DP1 AI158186NIAID NIH HHS HHSN272201700059C
6 · The paper itself

Abstract

Although infections among vaccinated individuals lead to milder COVID-19 symptoms relative to those in unvaccinated subjects, the specificity and durability of antibody responses elicited by breakthrough cases remain unknown. Here, we demonstrate that breakthrough infections induce serum-binding and -neutralizing antibody responses that are markedly more potent, durable, and resilient to spike mutations observed in variants than those in subjects who received only 2 doses of vaccine. However, we show that breakthrough cases, subjects who were vaccinated after infection, and individuals vaccinated three times have serum-neutralizing activity of comparable magnitude and breadth, indicating that an increased number of exposures to SARS-CoV-2 antigen(s) enhance the quality of antibody responses. Neutralization of SARS-CoV was moderate, however, underscoring the importance of developing vaccines eliciting broad sarbecovirus immunity for pandemic preparedness.

Indexed as

antibodiesbreakthrough infectionCOVID-19Delta variantneutralizationSARS-CoV-2vaccine

Identifiers

PMID35123650
PMCPMC8769922

What OpenQuestion holds

Textmetadata
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.