Evidence map›Paper›PMID 31185296›Full record

ArticlePapillomavirus research (Amsterdam, Netherlands)2019

Preclinical study of safety and immunogenicity of combined rubella and human papillomavirus vaccines: Towards enhancing vaccination uptake rates in developing countries.

Asmaa Gohar, Nourtan F Abdeltawab, Nahla Shehata, Magdy A Amin

Open access · goldAbstract read
In one paragraph

Article in Papillomavirus research (Amsterdam, Netherlands), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Asmaa GoharBiotechnology Control Unit, National Organization of Research and Control of Biologicals, Cairo, Egypt. Electronic address: asma.gohar@yahoo.com.
Nourtan F AbdeltawabDepartment of Microbiology and Immunology, Faculty of Pharmacy, Cairo University, Cairo, Egypt. Electronic address: nourtan.abdeltawab@pharma.cu.edu.eg.
Nahla ShehataBiotechnology Control Unit, National Organization of Research and Control of Biologicals, Cairo, Egypt. Electronic address: lr_egy@yahoo.com.
Magdy A AminDepartment of Microbiology and Immunology, Faculty of Pharmacy, Cairo University, Cairo, Egypt. Electronic address: magdy_biotek3@yahoo.com.
Cairo University · EGNational Organization for Drug Control and Research · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rubella vaccine was not part of national immunization programs (NIP) in several countries in the Middle East and North Africa (MENA), South-East Asia (SEA), and South Africa regions until the year 2000. Therefore, immunization coverage of females older than 20 years old in these countries has been the focus of national campaigns for rubella elimination in developing countries. Vaccines against human papillomavirus (HPV) are not part of NIPs in developing countries. To enhance the advantages of rubella-directed immunization campaigns and to increase HPV vaccine uptake in developing countries, this study aimed to test the stability, potency, efficacy and safety of a combined rubella and HPV vaccine. Female BALB/c mice were immunized subcutaneously with proposed combined HPV16/HPV18 VLP and rubella vaccine at weeks (W) 0, 3 then with HPV vaccine at W 7. Immunized mice developed antigen-specific antibodies against rubella and HPV significantly higher than mice immunized with rubella or HPV vaccine alone. The combined vaccine induced significantly higher splenocyte proliferation than control groups. In addition, pro-inflammatory cytokines IL-4, IL-6, IL-2, and IFNγ levels were significantly higher in mice immunized with the combined vaccine than control groups. Overall, the combined vaccine was safe and immunogenic offering antibody protection as well as eliciting a cellular immune response against rubella and HPV viruses in a single vaccine. This combined vaccine can be of great value to females above 20 years old in the SEA, MENA and South Africa regions offering coverage to rubella vaccine and a potential increase in HPV vaccine uptake rates after appropriate clinical testing.

Indexed as

Immunogenicity, VaccineAnimalsAntibodies, ViralAntigens, ViralCell LineCytokinesDeveloping CountriesDrug Evaluation, PreclinicalFemaleGuinea PigsHuman Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18HumansImmunizationImmunization ScheduleImmunoglobulin GInflammation MediatorsAntibodies, ViralAntigens, ViralCytokinesHuman Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18Immunoglobulin GInflammation MediatorsPapillomavirus VaccinesRubella VaccineAnimal modelAssessment of immunogenicityBALB/c miceCellular responseCombined vaccineDeveloping countriesHPVHumoral responseImmune responseImmunization scheduleImmunogenicityNational immunization programPreclinicalRubellaSafetyVaccine uptakeViral vaccines

Identifiers

PMID31185296
PMCPMC6586776
OpenAlexW2951573746

What OpenQuestion holds

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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.