Evidence map›Paper›PMID 35110410›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Immunogenicity of rVSVΔG-ZEBOV-GP Ebola vaccination in exposed and potentially exposed persons in the Democratic Republic of the Congo.

Nicole A Hoff, Anna Bratcher, J Daniel Kelly, Kamy Musene, Jean Paul Kompany, Michel Kabamba, Placide Mbala-Kingebeni, Bonnie Dighero-Kemp, Gregory Kocher, Elizabeth Elliott and 13 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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
–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

7 citing papers in PubMed.

  1. Article
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  5. Article
  6. Review
  7. Human vaccines & immunotherapeutics: news February 2022.Human vaccines & immunotherapeutics · 2022
    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

23 authors.

Nicole A HoffDepartment of Epidemiology, University of California, Los Angeles, CA 90095.ORCID 0000-0002-1770-6304
Anna BratcherDepartment of Epidemiology, University of California, Los Angeles, CA 90095.ORCID 0000-0001-5972-1249
J Daniel KellyDepartment of Epidemiology and Biostatistics, University of California, San Francisco, CA 94158.
Kamy MuseneDepartment of Epidemiology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of the Congo.
Jean Paul KompanyDepartment of Epidemiology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of the Congo.
Michel KabambaExpanded Programme for Immunization, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0003-3843-654X
Placide Mbala-KingebeniDepartment of Epidemiology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of the Congo.
Bonnie Dighero-KempIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD 21701.
Gregory KocherIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD 21701.
Elizabeth ElliottIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD 21701.
Cavan ReillyDivision of Biostatistics, University of Minnesota, Minneapolis, MN 55455.
Megan HalbrookDepartment of Epidemiology, University of California, Los Angeles, CA 90095.
Benoit Ilunga KebelaDivision of Disease Control, Ministry of Health, Kinshasa, Democratic Republic of Congo.
Adva GadothDepartment of Epidemiology, University of California, Los Angeles, CA 90095.ORCID 0000-0002-3217-2435
Guillaume Ngoie MwambaExpanded Programme for Immunization, Kinshasa, Democratic Republic of the Congo.
Merly TambuDepartment of Epidemiology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of the Congo.
David R McIlwainDepartment of Pathology, Stanford University, Stanford, CA 94304.
Patrick MukadiDepartment of Epidemiology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0001-9312-9345
Lisa E HensleyIntegrated Research Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD 21701.ORCID 0000-0003-1188-4342
Steve Ahuka-MundekeDepartment of Epidemiology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of the Congo.
George W RutherfordDepartment of Epidemiology and Biostatistics, University of California, San Francisco, CA 94158.ORCID 0000-0002-0707-8287
Jean Jacques Muyembe-TamfumDepartment of Epidemiology, National Institute of Biomedical Research, Kinshasa, Democratic Republic of the Congo.
Anne W RimoinDepartment of Epidemiology, University of California, Los Angeles, CA 90095; arimoin@ucla.edu.ORCID 0000-0002-0662-9067

Funding

Ebola modeling: behavior, asymptomatic infection, and contacts (2019-nCoV Admin Supplement)R01GM130900 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PORCO, TRAVIS CHRISTIAN · 2019 to 2022
$1.6M
Understanding the epidemiology and natural history of unrecognized Ebola virus infectionK23AI146268 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KELLY, JOHN DANIEL · 2019 to 2022
$748k
NIAID NIH HHS K23 AI146268NIAID NIH HHS L30 AI126521NIGMS NIH HHS R01 GM130900
6 · The paper itself

Abstract

Despite more than 300,000 rVSVΔG-ZEBOV-glycoprotein (GP) vaccine doses having been administered during Ebola virus disease (EVD) outbreaks in the Democratic Republic of the Congo (DRC) between 2018 and 2020, seroepidemiologic studies of vaccinated Congolese populations are lacking. This study examines the antibody response at 21 d and 6 mo postvaccination after single-dose rVSVΔG-ZEBOV-GP vaccination among EVD-exposed and potentially exposed populations in the DRC. We conducted a longitudinal cohort study of 608 rVSVΔG-ZEBOV-GP-vaccinated individuals during an EVD outbreak in North Kivu Province, DRC. Participants provided questionnaires and blood samples at three study visits (day 0, visit 1; day 21, visit 2; and month 6, visit 3). Anti-GP immunoglobulin G (IgG) antibody titers were measured in serum by the Filovirus Animal Nonclinical Group anti-Ebola virus GP IgG enzyme-linked immunosorbent assay. Antibody response was defined as an antibody titer that had increased fourfold from visit 1 to visit 2 and was above four times the lower limit of quantification at visit 2; antibody persistence was defined as a similar increase from visit 1 to visit 3. We then examined demographics for associations with follow-up antibody titers using generalized linear mixed models. A majority of the sample, 87.2%, had an antibody response at visit 2, and 95.6% demonstrated antibody persistence at visit 3. Being female and of young age was predictive of a higher antibody titer postvaccination. Antibody response and persistence after Ebola vaccination was robust in this cohort, confirming findings from outside of the DRC.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, ViralChildDemocratic Republic of the CongoDisease OutbreaksEbola VaccinesEbolavirusFemaleGlycoproteinsHemorrhagic Fever, EbolaHumansImmunogenicity, VaccineMaleAntibodies, ViralEbola VaccinesGlycoproteinsViral Envelope ProteinsDemocratic Republic of the CongoEbola vaccineEbola virus diseaseimmunogenicityrVSVΔG-ZEBOV-GP

Identifiers

PMID35110410
PMCPMC8833182

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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.