Evidence map›Paper›PMID 35865654›Full record

ArticleLancet regional health. Americas2022

Achieving high immunogenicity against poliovirus with fractional doses of inactivated poliovirus vaccine in Ecuador-results from a cross-sectional serological survey.

Gabriel Trueba, Vishali Jeyaseelan, Lazaro Lopez, Bernardo A Mainou, Yiting Zhang, Alvaro Whittembury, Alfredo Jose Olmedo Valarezo, Gonzalo Baquero, Rosa Romero de Aguinaga, Lucia Jeannete Zurita Salinas and 6 more

Open access · goldAbstract read
In one paragraph

Article in Lancet regional health. Americas, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 9 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

16 authors at 5 institutions in 3 countries.

Gabriel TruebaUniversity of San Francisco, Quito, Ecuador.
Vishali JeyaseelanPolio Eradication Department, World Health Organization, Avenue Appia 20, CH-1211 Genève 27, Geneva, Switzerland.
Lazaro LopezUniversity of San Francisco, Quito, Ecuador.
Bernardo A MainouDivision of Viral Diseases, Centres for Disease Control and Prevention, Atlanta, USA.
Yiting ZhangDivision of Viral Diseases, Centres for Disease Control and Prevention, Atlanta, USA.
Alvaro WhittemburyPan American Health Organization, Ecuador.
Alfredo Jose Olmedo ValarezoPan American Health Organization, Ecuador.
Gonzalo BaqueroNational Polio Certification Commission, Ecuador.
Rosa Romero de AguinagaNational Polio Certification Commission, Ecuador.
Lucia Jeannete Zurita SalinasNational Polio Certification Commission, Ecuador.
Maria Gabriela Santacruz ManchenoMinistry of Public Health, Ecuador.
Diana Elizabeth Medina ChachoMinistry of Public Health, Ecuador.
Emmanuelle QuentinUniversidad UTE, Ecuador.
Ana Elena ChevezImmunization Unit, Pan American Health Organization, Washington, USA.
Gloria Rey-BenitoImmunization Unit, Pan American Health Organization, Washington, USA.
Ondrej MachPolio Eradication Department, World Health Organization, Avenue Appia 20, CH-1211 Genève 27, Geneva, Switzerland.
Centers for Disease Control and Prevention · USUniversidad San Francisco de Quito · ECWorld Health Organization · CHWorld Health Organization Regional Office for the Americas · USUniversidad UTE · EC

Funding

World Health Organization 001
6 · The paper itself

Abstract

Background: In January 2018, Ecuador changed its routine immunization schedule by replacing one full dose of inactivated poliovirus vaccine (IPV) administered intramuscularly at 2 months of age with two doses of fractional IPV (1/5th of full dose, fIPV) administered intradermally at 2 and 4 months of age; and bivalent oral poliovirus vaccine (serotypes 1 and 3, bOPV) continues to be used. We compared seroprevalence and titres of polio antibodies achieved by the past and the current immunization schedules. Methods: This was a cross-sectional serological survey in children in Ecuador who received bOPV and either one IPV dose in 2017 or two fIPV doses in 2018. One blood sample was collected between October 2020 and March 2021 and analysed for presence of poliovirus neutralizing antibodies at CDC, Atlanta by microneutralization assay. Findings: We obtained 321 analysable samples from 329 (97·6%) enrolled children (160 received IPV and 161 fIPV). For serotype 2, seroprevalence was 50·0% (CI95%= 44·2-55·8%) for IPV and 83·2% (CI95%=78·5-87·1%) for fIPV recipients (p<0·001). Median antibody titers for serotype 2 were significantly lower for IPV than for fIPV recipients (3·0, CI95%= 3 - 3·5 vs. 4·8, CI95%= 4·5 - 5·2, p<0·001). Seroprevalence for serotypes 1 and 3 was above 90% and was not significantly different between IPV and fIPV recipients. Interpretation: Ecuador achieved significantly better poliovirus serotype 2 immunogenicity with two fIPV doses than with one IPV dose, while preserving vaccine supply and reducing costs. Our data provide further evidence that fIPV is a beneficial and potentially a cost-effective option in polio immunization. Funding: WHO obtained funds for the study from Rotary International.

Indexed as

EcuadorFractional dose inactivated poliovirus vaccinePoliomyelitisRoutine immunizationSeroprevalence assay

Identifiers

PMID35865654
PMCPMC9283112
OpenAlexW4220935134

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.