Evidence map›Paper›PMID 36016151›Full record

ArticleVaccines2022

Protection against Marburg Virus and Sudan Virus in NHP by an Adenovector-Based Trivalent Vaccine Regimen Is Correlated to Humoral Immune Response Levels.

Machteld M Tiemessen, Laura Solforosi, Liesbeth Dekking, Dominika Czapska-Casey, Jan Serroyen, Nancy J Sullivan, Ariane Volkmann, Maria Grazia Pau, Benoit Callendret, Hanneke Schuitemaker and 3 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

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  6. [Vaccinations for emerging and re-emerging viral diseases].Innere Medizin (Heidelberg, Germany) · 2024
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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

13 authors at 3 institutions in 3 countries.

Machteld M TiemessenJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Laura SolforosiJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Liesbeth DekkingJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Dominika Czapska-CaseyJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Jan SerroyenJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Nancy J SullivanVaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Ariane VolkmannBavarian Nordic GmbH, Fraunhoferstrasse 13, D-82152 Martinsried, Germany.
Maria Grazia PauJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Benoit CallendretJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Hanneke SchuitemakerJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.ORCID 0000-0001-8563-2266
Kerstin LuhnJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Roland ZahnJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Ramon RoozendaalJanssen Vaccines & Prevention B.V., Archimedesweg 6, 2333 CN Leiden, The Netherlands.
Janssen (Netherlands) · NLBavarian Nordic (Germany) · DENational Institutes of Health · US

Funding

National Institute of Allergy and Infectious Diseases HHSN272200800056C, HHSN272201000006I, HHSN272201200003I, HHSN272200800056C, HHSN272201000006I|HHSN27200007, HHSN272201200003I|HHSN2720000NIAID NIH HHS HHSN272200800056CNIAID NIH HHS HHSN272201200003I
6 · The paper itself

Abstract

The Marburg virus (MARV) and Sudan virus (SUDV) belong to the filovirus family. The sporadic human outbreaks occur mostly in Africa and are characterized by an aggressive disease course with high mortality. The first case of Marburg virus disease in Guinea in 2021, together with the increased frequency of outbreaks of Ebola virus (EBOV), which is also a filovirus, accelerated the interest in potential prophylactic vaccine solutions against multiple filoviruses. We previously tested a two-dose heterologous vaccine regimen (Ad26.Filo, MVA-BN-Filo) in non-human primates (NHP) and showed a fully protective immune response against both SUDV and MARV in addition to the already-reported protective effect against EBOV. The vaccine-induced glycoprotein (GP)-binding antibody levels appear to be good predictors of the NHP challenge outcome as indicated by the correlation between antibody levels and survival outcome as well as the high discriminatory capacity of the logistic model. Moreover, the elicited GP-specific binding antibody response against EBOV, SUDV, and MARV remains stable for more than 1 year. Overall, the NHP data indicate that the Ad26.Filo, MVA-BN-Filo regimen may be a good candidate for a prophylactic vaccination strategy in regions at high risk of filovirus outbreaks.

Indexed as

Ad26Ebola virusfilovirusglycoprotein (GP)–binding antibodyMarburg virusnon-human primate (NHP)Sudan virusvaccine

Identifiers

PMID36016151
PMCPMC9412258
OpenAlexW4292513041

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.