Evidence map›Paper›PMID 25224011›Full record

ArticleAntimicrobial agents and chemotherapy2014

Ganciclovir inhibits human adenovirus replication and pathogenicity in permissive immunosuppressed Syrian hamsters.

Baoling Ying, Ann E Tollefson, Jacqueline F Spencer, Lata Balakrishnan, Stephen Dewhurst, Cristina Capella, R Mark L Buller, Karoly Toth, William S M Wold

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  15. Filociclovir Is a PotentAntimicrobial agents and chemotherapy · 2020
    Article
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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

9 authors at 3 institutions in 1 country.

Baoling YingSaint Louis University School of Medicine, Department of Molecular Microbiology & Immunology, St. Louis, Missouri, USA.
Ann E TollefsonSaint Louis University School of Medicine, Department of Molecular Microbiology & Immunology, St. Louis, Missouri, USA.
Jacqueline F SpencerSaint Louis University School of Medicine, Department of Molecular Microbiology & Immunology, St. Louis, Missouri, USA.
Lata BalakrishnanUniversity of Rochester Medical Center, Department of Biochemistry and Biophysics, Rochester, New York, USA.
Stephen DewhurstUniversity of Rochester Medical Center, Department of Microbiology & Immunology, Rochester, New York, USA.
Cristina CapellaThe Ohio State University, Nationwide Childrens' Hospital, Columbus, Ohio, USA.
R Mark L BullerSaint Louis University School of Medicine, Department of Molecular Microbiology & Immunology, St. Louis, Missouri, USA.
Karoly TothSaint Louis University School of Medicine, Department of Molecular Microbiology & Immunology, St. Louis, Missouri, USA toth@slu.edu.
William S M WoldSaint Louis University School of Medicine, Department of Molecular Microbiology & Immunology, St. Louis, Missouri, USA.
Saint Louis University · USUniversity of Rochester Medical Center · USNationwide Children's Hospital · US

Funding

NIAID NIH HHS HHSN272201000021CNIAID NIH HHS HHSN272201000021I
6 · The paper itself

Abstract

Adenovirus infections of immunocompromised patients can develop into deadly multiorgan or systemic disease. The virus is especially threatening for pediatric allogeneic hematopoietic stem cell transplant recipients; according to some studies, 10% or more of these patients succumb to disease resulting from adenovirus infection. At present, there is no drug approved for the treatment or prevention of adenovirus infections. Compounds that are approved to treat other virus infections are used off-label to combat adenovirus, but only anecdotal evidence of the efficacy of these drugs exists. Ganciclovir, a drug approved for the treatment of herpesvirus infection, was previously reported to be effective against human adenoviruses in vitro. To model adenovirus infections in immunocompromised humans, we examined ganciclovir's efficacy in immunosuppressed Syrian hamsters intravenously infected with type 5 human adenovirus (Ad5). This animal model is permissive for Ad5 replication, and the animals develop symptoms similar to those seen in humans. We demonstrate that ganciclovir suppresses Ad5 replication in the liver of infected hamsters and that it mitigates the consequences of Ad5 infections in these animals when administered prophylactically or therapeutically. We show that ganciclovir inhibits Ad5 DNA synthesis and late gene expression. The mechanism of action for the drug is not clear; preliminary data suggest that it exerts its antiadenoviral effect by directly inhibiting the adenoviral DNA polymerase. While more extensive studies are required, we believe that ganciclovir is a promising drug candidate to treat adenovirus infections. Brincidofovir, a drug with proven activity against Ad5, was used as a positive control in the prophylactic experiment.

Indexed as

Immunocompromised HostAdenoviridae InfectionsAdenoviruses, HumanAnimalsAntiviral AgentsBody WeightCell Line, TumorCytosineDNA-Directed DNA PolymeraseFemaleGanciclovirGene ExpressionHumansMaleMesocricetusOrganophosphonatesAntiviral AgentsbrincidofovirCytosineDNA-Directed DNA PolymeraseGanciclovirOrganophosphonatesTransaminasesViral Proteins

Identifiers

PMID25224011
PMCPMC4249575
OpenAlexW2001843565

What OpenQuestion holds

Textmetadata
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.