Evidence map›Paper›PMID 36146536›Full record

ArticleVaccines2022

Durability of Protection Post-Primary COVID-19 Vaccination in the United States.

Amanda Zheutlin, Miles Ott, Ran Sun, Natalia Zemlianskaia, Craig S Meyer, Meagan Rubel, Jennifer Hayden, Breno Neri, Tripthi Kamath, Najat Khan and 2 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  11. Adenovirus-based vaccines-a platform for pandemic preparedness against emerging viral pathogens.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
  12. Article
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

12 authors at 2 institutions in 1 country.

Amanda ZheutlinData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Miles OttData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Ran SunData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Natalia ZemlianskaiaData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Craig S MeyerData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Meagan RubelData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.ORCID 0000-0002-4246-9531
Jennifer HaydenData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Breno NeriData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Tripthi KamathData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Najat KhanData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Sebastian SchneeweissDivision of Pharmacoepidemiology, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02120, USA.
Khaled SarsourData Sciences, Research & Development, Janssen Pharmaceuticals, Titusville, NJ 08560, USA.
Janssen (United States) · USBrigham and Women's Hospital · US

Funding

Janssen (United States) NA
6 · The paper itself

Abstract

The durability of immune responses after COVID-19 vaccination will drive long-term vaccine effectiveness across settings and may differ by vaccine type. To determine durability of protection of COVID-19 vaccines (BNT162b2, mRNA-1273, and Ad26.COV2.S) following primary vaccination in the United States, a matched case-control study was conducted in three cohorts between 1 January and 7 September 2021 using de-identified data from a database covering 168 million lives. Odds ratios (ORs) for developing outcomes of interest (breakthrough SARS-CoV-2 infection, hospitalization, or intensive care unit admission) were determined for each vaccine (no direct comparisons). In total, 17,017,435 individuals were identified. Relative to the baseline, stable protection was observed for Ad26.COV2.S against infections (OR [95% confidence interval (CI)], 1.31 [1.18-1.47]) and hospitalizations (OR [95% CI], 1.25 [0.86-1.80]). Relative to the baseline, protection waned over time against infections for BNT162b2 (OR [95% CI], 2.20 [2.01-2.40]) and mRNA-1273 (OR [95% CI], 2.07 [1.87-2.29]) and against hospitalizations for BNT162b2 (OR [95% CI], 2.38 [1.79-3.17]). Baseline protection remained stable for intensive care unit admissions for all three vaccines. Calculated baseline VE was consistent with published literature. This study suggests that the three vaccines in three separate populations may have different durability profiles.

Indexed as

Ad26.COV2.SBNT162b2durabilitymRNA-1273vaccine effectiveness

Identifiers

PMID36146536
PMCPMC9505933
OpenAlexW4295094955

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.