Evidence map›Paper›PMID 42509604›Full record

ArticleThe Pediatric infectious disease journal2026

Evaluation of Rotavirus Vaccine Effectiveness by Severity of Rotavirus Disease: Findings From the MNSSTER-V Project.

Mary C Moran, Jordan Cates, Neha Balachandran, Jazmina Umana, Helah Safi, Hammarskjold Makhuza, Volga Iniguez, Nguyen Van Trang, Isidore Bonkoungou, Cissy Nalunkuma and 21 more

Abstract read
In one paragraph

Article in The Pediatric infectious disease journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

31 authors.

Mary C MoranFrom the Viral Gastroenteritis Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Atlanta, Georgia.ORCID 0000-0002-6456-082
Jordan CatesFrom the Viral Gastroenteritis Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Atlanta, Georgia.
Neha BalachandranFrom the Viral Gastroenteritis Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Atlanta, Georgia.
Jazmina UmanaExpanded Program Immunization, Managua, Nicaragua.
Helah SafiJS Consultancy, Kabul, Afghanistan.
Hammarskjold MakhuzaChild and Adolescent Health Unit, Sally Mugabe Central Hospital, University of Zimbabwe, Harare, Zimbabwe.
Volga IniguezInstituto de Biologia Molecular y Biotecnologia, Universidad Mayor de San Andres, La Paz, Bolivia.
Nguyen Van TrangNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Isidore BonkoungouCentral Reference Laboratory, National Public Health Institute, Ouagadougou, Burkina Faso.
Cissy NalunkumaPaediatrics and Child Health, Lubaga Hospital, Kampala, Uganda.
Christophe Luhata LungayoProgramme élargi de Vaccination, Kinshasa, Democratic Republic of the Congo.
Christabel Enweronu-LaryeaDepartment of Child Health, University of Ghana Medical School, Accra, Ghana.
Inácio MandomandoCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.
Julia Liliane RabobaCHU Mère Enfant Tsaralalàna, Antananarivo, Madagascar.
Margaret MokomaneFaculty of Health Sciences, School of Allied Health Professions, University of Botswana, Gaborone, Botswana.
Jeannine UwimanaDepartment of Pathology, Kigali University Teaching Hospital, Institute of Applied Sciences, Kigali, Rwanda.
Kofi N'ZueWorld Health Organization Cote d'Ivoire Country Office, Abidjan, Côte d'Ivoire.
Ingrid Contreras-RoldánCenter for Health Studies, Universidad del Valle de Guatemala, Guatemala City, Guatemala.
Richard OmoreKenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
Michelle J GroomeSouth Africa Medical Research Council Vaccines and Infectious Diseases Analytics Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Stela GheorghitaNational Center for Public Health, Ministry of Health of the Republic of Moldova, Chisinau, Moldova.
Anvar NazurdinovDepartment of Epidemiology of the State Educational Institution "Avicenna Tajik State Medical University", Dushanbe, Tajikistan.
Fausta MichaelMinistry of Health, Community Development, Gender, Elderly and Children, Dar es Salaam, Tanzania.
Renat LatipovInstitute of Virology, Tashkent, Uzbekistan.
Gloria Rey-BenitoPan American Health Organization (PAHO), Washington, District of Columbia.
Goitom WeldegebrielWHO/AFRO Inter Country Support Team, South and East Africa, Harare, Zimbabwe.
Jason M MwendaDiarrhea Pathogens Research Unit, Department of Virology, Sefako Makgatho Health Sciences University, Pretoria, South Africa.
Eleanor BurnettFrom the Viral Gastroenteritis Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Atlanta, Georgia.
Umesh D ParasharFrom the Viral Gastroenteritis Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Atlanta, Georgia.
Jacqueline E TateFrom the Viral Gastroenteritis Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Atlanta, Georgia.
Multi-National Subpopulations Study to Evaluate Rotavirus Vaccines (MNSSTER-V) Project Working Group

Funding

Intramural CDC HHS CC999999Wellcome Trust
6 · The paper itself

Abstract

backgroundSince the introduction of rotavirus vaccines, acute gastroenteritis (AGE) hospitalizations due to rotavirus have decreased globally; however, vaccine effectiveness (VE) differs by country, age and disease severity. We evaluated rotavirus VE by disease severity in different age groups and under-5 childhood mortality (U5M) strata.

methodsThe Vesikari score is a common measure of AGE disease severity. A modified Vesikari Score (mVS) was calculated for 18,426 children with medically attended AGE across 16 countries from the Multi-National Subpopulations Study To Evaluate Rotavirus Vaccines dataset. Using a test-negative case-control design (cases had rotavirus-positive AGE and controls had rotavirus-negative AGE), we calculated complete rotavirus series VE against different severity categories among children 6-59 months old, stratified by age and country U5M level, respectively.

resultsVE increased with increasing disease severity: 38% (95% confidence interval [CI]:17-53) for mild/moderate disease versus 58% (95% CI: 50-64) for severe/very severe disease, and this pattern persisted with stratification by age and U5M. Among children with severe/very severe disease, VE was higher in infants aged 6-11 months (62%, 95% CI: 51-70) compared with children aged 24-59 months (11%, 95% CI: -78 to 56), and lower among children in the highest U5M strata (44%, 95% CI: 26-58) compared to children in the high U5M strata (60%, 95% CI: 47-69).

conclusionsRotavirus vaccines provide the greatest protection against very severe rotavirus disease. VE remains lower in countries with higher U5M levels, even among children with very severe rotavirus disease, highlighting the need for improved vaccine performance in countries with high disease burden.

Indexed as

disease severityrotavirusvaccine effectiveness

Identifiers

PMID42509604
PMCPMC13647712

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