Evidence map›Paper›PMID 34469243›Full record

ArticleJournal of virology2021

Human AdV-20-42-42, a Promising Novel Adenoviral Vector for Gene Therapy and Vaccine Product Development.

Mónika Z Ballmann, Svjetlana Raus, Ruben Engelhart, Győző L Kaján, Abdelaziz Beqqali, Patrick W F Hadoke, Chantal van der Zalm, Tibor Papp, Lijo John, Selina Khan and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-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

10 citing papers in PubMed, 16 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

20 authors at 4 institutions in 3 countries.

Mónika Z BallmannBatavia Biosciences B.V., Leiden, The Netherlands.
Svjetlana RausCentre for Cardiovascular Sciences, University of Edinburghgrid.4305.2, Edinburgh, United Kingdom.
Ruben EngelhartBatavia Biosciences B.V., Leiden, The Netherlands.
Győző L KajánDepartment of Clinical Microbiology, Division of Virology, Umeå University, Umeå, Sweden.
Abdelaziz BeqqaliCentre for Cardiovascular Sciences, University of Edinburghgrid.4305.2, Edinburgh, United Kingdom.
Patrick W F HadokeCentre for Cardiovascular Sciences, University of Edinburghgrid.4305.2, Edinburgh, United Kingdom.
Chantal van der ZalmBatavia Biosciences B.V., Leiden, The Netherlands.
Tibor PappJanssen Vaccines and Prevention B.V., Leiden, The Netherlands.
Lijo JohnDepartment of Clinical Microbiology, Division of Virology, Umeå University, Umeå, Sweden.
Selina KhanJanssen Vaccines and Prevention B.V., Leiden, The Netherlands.
Satish BoedhoeJanssen Vaccines and Prevention B.V., Leiden, The Netherlands.
Katarina DanskogDepartment of Clinical Microbiology, Division of Virology, Umeå University, Umeå, Sweden.
Lars FrängsmyrDepartment of Clinical Microbiology, Division of Virology, Umeå University, Umeå, Sweden.
Jerome CustersJanssen Vaccines and Prevention B.V., Leiden, The Netherlands.
Wilfried A M BakkerBatavia Biosciences B.V., Leiden, The Netherlands.ORCID 0000-0001-8731-6689
Hilde M van der SchaarBatavia Biosciences B.V., Leiden, The Netherlands.
Niklas ArnbergDepartment of Clinical Microbiology, Division of Virology, Umeå University, Umeå, Sweden.
Angelique A C LemckertBatavia Biosciences B.V., Leiden, The Netherlands.
Menzo HavengaBatavia Biosciences B.V., Leiden, The Netherlands.
Andrew H BakerCentre for Cardiovascular Sciences, University of Edinburghgrid.4305.2, Edinburgh, United Kingdom.ORCID 0000-0003-1441-5576
Batavia Biosciences (Netherlands) · NLUmeå University · SEJanssen (Netherlands) · NLUniversity of Edinburgh · GB

Funding

EC | H2020 | H2020 PRIORITÉ Défis de société | H2020 Health (HEALTH) 825670FP7 People: Marie-Curie Actions (PEOPLE) 324325Magyar Tudományos Akadémia (MTA) János Bolyai Research ScholarshipNational Research, Development and Innovation Office OTKA NN128309
6 · The paper itself

Abstract

Preexisting immune responses toward adenoviral vectors limit the use of a vector based on particular serotypes and its clinical applicability for gene therapy and/or vaccination. Therefore, there is a significant interest in vectorizing novel adenoviral types that have low seroprevalence in the human population. Here, we describe the discovery and vectorization of a chimeric human adenovirus, which we call HAdV-20-42-42. Full-genome sequencing revealed that this virus is closely related to human serotype 42, except for the penton base, which is derived from serotype 20. The HAdV-20-42-42 vector could be propagated stably to high titers on existing E1-complementing packaging cell lines. Receptor-binding studies revealed that the vector utilized both CAR and CD46 as receptors for cell entry. Furthermore, the HAdV-20-42-42 vector was potent in transducing human and murine cardiovascular cells and tissues, irrespective of the presence of blood coagulation factor X.

Indexed as

Adenoviruses, HumanGenetic VectorsA549 CellsAnimalsGenetic TherapyHEK293 CellsHumansMaleMiceSeroepidemiologic StudiesVaccine Developmentcell and tissue transductionexpression vectorlow seroprevalencenovel adenovirus serotypepotent T-cell responses

Identifiers

PMID34469243
PMCPMC8549523
OpenAlexW3196480122

What OpenQuestion holds

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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.