Evidence map›Paper›PMID 34375308›Full record

ArticleThe Journal of clinical investigation2021

Dominance of Alpha and Iota variants in SARS-CoV-2 vaccine breakthrough infections in New York City.

Ralf Duerr, Dacia Dimartino, Christian Marier, Paul Zappile, Guiqing Wang, Jennifer Lighter, Brian Elbel, Andrea B Troxel, Adriana Heguy

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 54 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

9 authors at 3 institutions in 1 country.

Ralf DuerrDepartment of Microbiology, NYU Grossman School of Medicine, New York, New York, USA.
Dacia DimartinoGenome Technology Center, Office of Science and Research, NYU Langone Health, New York, New York, USA.
Christian MarierGenome Technology Center, Office of Science and Research, NYU Langone Health, New York, New York, USA.
Paul ZappileGenome Technology Center, Office of Science and Research, NYU Langone Health, New York, New York, USA.
Guiqing WangDepartment of Pathology.
Jennifer LighterDepartment of Pediatric Infectious Diseases, and.
Brian ElbelDepartment of Population Health, NYU Grossman School of Medicine, New York, New York, USA.
Andrea B TroxelDepartment of Population Health, NYU Grossman School of Medicine, New York, New York, USA.
Adriana HeguyGenome Technology Center, Office of Science and Research, NYU Langone Health, New York, New York, USA.
New York Genome Center · USNew York University · USPediatric Infectious Diseases Society · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
NCI NIH HHS P30 CA016087
6 · The paper itself

Abstract

The efficacy of COVID-19 mRNA vaccines is high, but breakthrough infections still occur. We compared the SARS-CoV-2 genomes of 76 breakthrough cases after full vaccination with BNT162b2 (Pfizer/BioNTech), mRNA-1273 (Moderna), or JNJ-78436735 (Janssen) to unvaccinated controls (February-April 2021) in metropolitan New York, including their phylogenetic relationship, distribution of variants, and full spike mutation profiles. The median age of patients in the study was 48 years; 7 required hospitalization and 1 died. Most breakthrough infections (57/76) occurred with B.1.1.7 (Alpha) or B.1.526 (Iota). Among the 7 hospitalized cases, 4 were infected with B.1.1.7, including 1 death. Both unmatched and matched statistical analyses considering age, sex, vaccine type, and study month as covariates supported the null hypothesis of equal variant distributions between vaccinated and unvaccinated in χ2 and McNemar tests (P > 0.1), highlighting a high vaccine efficacy against B.1.1.7 and B.1.526. There was no clear association among breakthroughs between type of vaccine received and variant. In the vaccinated group, spike mutations in the N-terminal domain and receptor-binding domain that have been associated with immune evasion were overrepresented. The evolving dynamic of SARS-CoV-2 variants requires broad genomic analyses of breakthrough infections to provide real-life information on immune escape mediated by circulating variants and their spike mutations.

Indexed as

Evolution, MolecularMutationSARS-CoV-2Spike Glycoprotein, Coronavirus2019-nCoV Vaccine mRNA-1273Ad26COVS1AdultAgedAged, 80 and overBNT162 VaccineCOVID-19COVID-19 VaccinesFemaleHumansImmune EvasionMale2019-nCoV Vaccine mRNA-1273Ad26COVS1BNT162 VaccineCOVID-19 VaccinesSpike Glycoprotein, CoronavirusCOVID-19EpidemiologyMolecular biology

Identifiers

PMID34375308
PMCPMC8439605
OpenAlexW3191934781

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.