Evidence map›Paper›PMID 36727201›Full record

ReviewHuman vaccines & immunotherapeutics2023

Evidence synthesis and pooled analysis of vaccine effectiveness for COVID-19 mRNA vaccine BNT162b2 as a heterologous booster after inactivated SARS-CoV-2 virus vaccines.

Moe H Kyaw, Julia Spinardi, Ling Zhang, Helen May Lin Oh, Amit Srivastava

Open access · goldAbstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 3 countries.

Moe H KyawVaccine Medical Affairs, Emerging Markets, Pfizer Inc, Gaithersburg, MD, USA.ORCID 0000-0002-7633-271X
Julia SpinardiVaccine Medical Affairs, Emerging Markets, Pfizer Inc, Sao Paulo, Brazil.
Ling ZhangReal World Evidence Analytics Center of Excellence, Boehringer Ingelheim, Ridgefield, CT, USA.
Helen May Lin OhDepartment of Infectious Diseases, Changi General Hospital, Singapore.
Amit SrivastavaOrbital Therapeutics, Cambridge, MA, USA.ORCID 0000-0002-2510-5058
Pfizer (United States) · USBoehringer Ingelheim (Egypt) · EGChangi General Hospital · SGOrbital Research (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction of primary COVID-19 vaccination has helped reduce severe disease and death caused by SARS-CoV-2 infection. Understanding the protection conferred by heterologous booster regimens informs alternative vaccination strategies that enable programmatic resilience and can catalyze vaccine confidence and coverage. Inactivated SARS-CoV-2 vaccines are among the most widely used vaccines worldwide. This review synthesizes the available evidence identified as of May 26, 2022, on the safety, immunogenicity, and effectiveness of a heterologous BNT162b2 (Pfizer-BioNTech) mRNA vaccine booster dose after an inactivated SARS-CoV-2 vaccine primary series, to help protect against COVID-19. Evidence showed that the heterologous BNT16b2 mRNA vaccine booster enhances immunogenicity and improves vaccine effectiveness against COVID-19, and no new safety concerns were identified with heterologous inactivated primary series with mRNA booster combinations.

Indexed as

COVID-19COVID-19 VaccinesBNT162 VaccineHumansmRNA VaccinesSARS-CoV-2Vaccine EfficacyBNT162 VaccineCOVID-19 VaccinesmRNA VaccinesBNT162b2COVID-19effectivenessheterologous boosterinactivated virus vaccinemRNA vaccine

Identifiers

PMID36727201
PMCPMC9980688
OpenAlexW4318921945

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.