Evidence map›Paper›PMID 35339308›Full record

ArticleVaccine2023

Analysis of population immunity to poliovirus following cessation of trivalent oral polio vaccine.

Arend Voorman, Hil Lyons, Caroline Bennette, Stephanie Kovacs, Jeevan K Makam, John F Vertefeuille, Graham Tallis

Open access · hybridAbstract read
In one paragraph

Article in Vaccine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
4.3field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 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

7 authors at 2 institutions in 1 country.

Arend VoormanThe Bill and Melinda Gates Foundation, 500 5th Ave N, Seattle, WA 98109, USA. Electronic address: arend.voorman@gatesfoundation.org.
Hil LyonsThe Bill and Melinda Gates Foundation, 500 5th Ave N, Seattle, WA 98109, USA; Institute for Disease Modeling, Global Health Division, Bill and Melinda Gates Foundation (BMGF), 500 5th Ave N, Seattle, WA 98109, USA.
Caroline BennetteThe Bill and Melinda Gates Foundation, 500 5th Ave N, Seattle, WA 98109, USA; Institute for Disease Modeling, Global Health Division, Bill and Melinda Gates Foundation (BMGF), 500 5th Ave N, Seattle, WA 98109, USA.
Stephanie KovacsCenters for Disease Control and Prevention (CDC), 1600 Clifton Road, Atlanta, GA 30329, USA.
Jeevan K MakamUnited Nations Children's Fund (UNICEF), 3 United Nations Plaza, New York, NY 10017, USA.
John F VertefeuilleCenters for Disease Control and Prevention (CDC), 1600 Clifton Road, Atlanta, GA 30329, USA.
Graham TallisPolio Eradication, World Health Organization (WHO), Avenue Appia 20, 1202 Genève, Switzerland.
Centers for Disease Control and Prevention · USUnited Nations Children's Fund · US

Funding

Intramural CDC HHS CC999999World Health Organization 001
6 · The paper itself

Abstract

backgroundThe global withdrawal of trivalent oral poliovirus vaccine (OPV) (tOPV, containing Sabin poliovirus strains serotypes 1, 2 and 3) from routine immunization, and the introduction of bivalent OPV (bOPV, containing Sabin poliovirus strains serotypes 1 and 3) and trivalent inactivated poliovirus vaccine (IPV) into routine immunization was expected to improve population serologic and mucosal immunity to types 1 and 3 poliovirus, while population mucosal immunity to type 2 poliovirus would decline. However, over the period since tOPV withdrawal, the implementation of preventive bOPV supplementary immunization activities (SIAs) has decreased, while outbreaks of type 2 circulating vaccine derived poliovirus (cVDPV2) have required targeted use of monovalent type 2 OPV (mOPV2).

methodsWe develop a dynamic model of OPV-induced immunity to estimate serotype-specific, district-level immunity for countries in priority regions and characterize changes in immunity since 2016. We account for the changes in routine immunization schedules and varying implementation of preventive and outbreak response SIAs, assuming homogenous coverages of 50% and 80% for SIAs.

resultsIn areas with strong routine immunization, the switch from tOPV to bOPV has likely resulted in gains in population immunity to types 1 and 3 poliovirus. However, we estimate that improved immunogenicity of new schedules has not compensated for declines in preventive SIAs in areas with weak routine immunization. For type 2 poliovirus, without tOPV in routine immunization or SIAs, mucosal immunity has declined nearly everywhere, while use of mOPV2 has created highly heterogeneous population immunity for which it is important to take into account when responding to cVDPV2 outbreaks.

conclusionsThe withdrawal of tOPV and declining allocations of resources for preventive bOPV SIAs have resulted in reduced immunity in vulnerable areas to types 1 and 3 poliovirus and generally reduced immunity to type 2 poliovirus in the regions studied, assuming homogeneous coverages of 50% and 80% for SIAs. The very low mucosal immunity to type 2 poliovirus generates substantially greater risk for further spread of cVDPV2 outbreaks. Emerging gaps in immunity to all serotypes will require judicious targeting of limited resources to the most vulnerable populations by the Global Polio Eradication Initiative (GPEI).

Indexed as

PoliomyelitisPoliovirusHumansPoliovirus Vaccine, InactivatedPoliovirus Vaccine, OralSerogroupVaccinationPoliovirus Vaccine, InactivatedPoliovirus Vaccine, OralDisease ModelingPolioPopulation immunity

Identifiers

PMID35339308
PMCPMC10973941
OpenAlexW4220948925

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.