Evidence map›Paper›PMID 34888672›Full record

SynthesisThe Journal of infectious diseases2022

Comparative Immunogenicity and Effectiveness of mRNA-1273, BNT162b2, and Ad26.COV2.S COVID-19 Vaccines.

Vivek Naranbhai, Wilfredo F Garcia-Beltran, Christina C Chang, Cristhian Berrios Mairena, Julia C Thierauf, Grace Kirkpatrick, Maristela L Onozato, Ju Cheng, Kerri J St Denis, Evan C Lam and 15 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in The Journal of infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 3 pooled it
7.5field-weighted citation impact, top 2% 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

102 citing papers in PubMed, 3 syntheses or guidelines pooled it, 131 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 3 institutions in 3 countries.

Vivek NaranbhaiDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0003-4281-8882
Wilfredo F Garcia-BeltranDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Christina C ChangCenter for the AIDS Programme of Research in South Africa, Durban, South Africa.
Cristhian Berrios MairenaDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Julia C ThieraufDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Grace KirkpatrickDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Maristela L OnozatoDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Ju ChengDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Kerri J St DenisRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts, USA.
Evan C LamRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts, USA.
Clarety KasekeRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts, USA.
Rhoda Tano-MenkaRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts, USA.
Diane YangDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Maia PavlovicDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Wendy YangDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Alexander KuiDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Tyler E MillerDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Michael G AstudilloDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Jennifer E CahillDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Anand S DigheDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
David J GregoryVaccine and Immunotherapy Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Mark C PoznanskyDepartment of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Gaurav D GaihaRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts, USA.
Alejandro B BalazsRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts, USA.
A John IafrateDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Massachusetts General Hospital · USRagon Institute of MGH, MIT and Harvard · USCentre for the AIDS Programme of Research in South Africa · ZA

Funding

Engineering Humoral Immunity to Functionally Cure HIV InfectionDP2DA040254 · NIDA · MASSACHUSETTS GENERAL HOSPITAL · PI BALAZS, ALEJANDRO BENJAMIN · 2015 to 2015
$2.6M
NIDA NIH HHS DP2 DA040254
6 · The paper itself

Abstract

backgroundUnderstanding immunogenicity and effectiveness of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines is critical to guide rational use.

methodsWe compared the immunogenicity of mRNA-1273, BNT-162b2, and Ad26.COV2.S in healthy ambulatory adults. We performed an inverse-variance meta-analysis of population-level effectiveness from public health reports in > 40 million individuals.

resultsA single dose of either mRNA vaccine yielded comparable antibody and neutralization titers to convalescent individuals. Ad26.COV2.S yielded lower antibody concentrations and frequently undetectable neutralization titers. Bulk and cytotoxic T-cell responses were higher in mRNA1273 and BNT162b2 than Ad26.COV2.S recipients. Regardless of vaccine, <50% of vaccinees demonstrated CD8+ T-cell responses. Antibody concentrations and neutralization titers increased comparably after the first dose of either vaccine, and further in recipients of a second dose. Prior infection was associated with high antibody concentrations and neutralization even after a single dose and regardless of vaccine. Neutralization of Beta, Gamma, and Delta strains were poorer regardless of vaccine. In meta-analysis, relative to mRNA1273 the effectiveness of BNT162b2 was lower against infection and hospitalization, and Ad26COV2.S was lower against infection, hospitalization, and death.

conclusionsVariation in the immunogenicity correlates with variable effectiveness of the 3 vaccines deployed in the United States.

Indexed as

Ad26COVS1COVID-192019-nCoV Vaccine mRNA-1273AdultBNT162 VaccineCOVID-19 VaccinesHumansImmunogenicity, VaccinemRNA VaccinesSARS-CoV-2Vaccines, Synthetic2019-nCoV Vaccine mRNA-1273Ad26COVS1BNT162 VaccineCOVID-19 VaccinesmRNA VaccinesVaccines, SyntheticAd26.COV2.SBNT162b2deatheffectivenesshospitalizationimmunogenicitymRNA-1273neutralizationSARS CoV-2T cells

Identifiers

PMID34888672
PMCPMC8689763
OpenAlexW4200498553

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.