Evidence map›Paper›PMID 33766944›Full record

ArticleScience (New York, N.Y.)2021

mRNA vaccination boosts cross-variant neutralizing antibodies elicited by SARS-CoV-2 infection.

Leonidas Stamatatos, Julie Czartoski, Yu-Hsin Wan, Leah J Homad, Vanessa Rubin, Hayley Glantz, Moni Neradilek, Emilie Seydoux, Madeleine F Jennewein, Anna J MacCamy and 9 more

Open access · hybridAbstract readEditorial
In one paragraph

Article in Science (New York, N.Y.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 386 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
386citing papers in PubMed, 1 pooled it
37.3field-weighted citation impact, top 1% 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

386 citing papers in PubMed, 1 synthesis or guideline pooled it, 616 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 2 countries.

Leonidas StamatatosFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA. amcguire@fredhutch.org lstamata@fredhutch.org jmcelrat@fredhutch.org.ORCID https://orcid.org/0000-0002-1106-7097
Julie CzartoskiFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0002-4344-6390
Yu-Hsin WanFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0003-2826-9928
Leah J HomadFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0001-8421-6519
Vanessa RubinFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0003-2134-0576
Hayley GlantzFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0002-1017-3488
Moni NeradilekFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0002-3154-6597
Emilie SeydouxFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0003-1021-4056
Madeleine F JenneweinFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0001-6633-7413
Anna J MacCamyFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0001-5552-9209
Junli FengFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.
Gregory MizeFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0003-4680-1893
Stephen C De RosaFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0003-3871-4618
Andrés FinziCentre de Recherche du CHUM, Montréal, QC, Canada.ORCID https://orcid.org/0000-0002-4992-5288
Maria P LemosFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0002-3530-9310
Kristen W CohenFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0002-8901-9941
Zoe MoodieFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.ORCID https://orcid.org/0000-0001-8701-2001
M Juliana McElrathFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA. amcguire@fredhutch.org lstamata@fredhutch.org jmcelrat@fredhutch.org.ORCID https://orcid.org/0000-0003-2276-7117
Andrew T McGuireFred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA. amcguire@fredhutch.org lstamata@fredhutch.org jmcelrat@fredhutch.org.ORCID https://orcid.org/0000-0003-1841-6859
Fred Hutch Cancer Center · USUniversity of Washington · USCentre Hospitalier de l’Université de Montréal · CA

Funding

LC: HIV Vaccine Trials NetworkUM1AI068618 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Margaret Juliana McElrath · 2011 to 2026
$483.6M
SDMC: HIV Vaccine Trials NetworkUM1AI068635 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Peter B. Gilbert, Yunda Huang · 2011 to 2026
$385.9M
Seattle Vaccine Trials UnitUM1AI069481 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Rachel Ann Bender Ignacio, Margaret Juliana McElrath · 2012 to 2026
$24.4M
NIAID NIH HHS UM1 AI068618NIAID NIH HHS UM1 AI068635NIAID NIH HHS UM1 AI069481
6 · The paper itself

Abstract

Emerging SARS-CoV-2 variants have raised concerns about resistance to neutralizing antibodies elicited by previous infection or vaccination. We examined whether sera from recovered and naïve donors collected prior to, and following immunizations with existing mRNA vaccines, could neutralize the Wuhan-Hu-1 and B.1.351 variants. Pre-vaccination sera from recovered donors neutralized Wuhan-Hu-1 and sporadically neutralized B.1.351, but a single immunization boosted neutralizing titers against all variants and SARS-CoV-1 by up to 1000-fold. Neutralization was due to antibodies targeting the receptor binding domain and was not boosted by a second immunization. Immunization of naïve donors also elicited cross-neutralizing responses, but at lower titers. Our study highlights the importance of vaccinating both uninfected and previously infected persons to elicit cross-variant neutralizing antibodies.

Identifiers

PMID33766944
PMCPMC8139425
OpenAlexW3136570200

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.