Evidence map›Paper›PMID 42303049›Full record

ArticleAntiviral research2026

Drug combination treatment as a strategy for inhibiting human adenovirus replication.

Mackenzie J Dodge, Katelyn M MacNeil, Tanner M Tessier, Andris M Evans, Kaitlyn R Palmateer, Jason B Weinberg, Joe S Mymryk

Abstract read
In one paragraph

Article in Antiviral research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Mackenzie J DodgeDepartment of Microbiology & Immunology, University of Western Ontario, London, ON, Canada.
Katelyn M MacNeilDepartment of Microbiology & Immunology, University of Western Ontario, London, ON, Canada.
Tanner M TessierDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Pennsylvania, USA.
Andris M EvansDepartment of Microbiology & Immunology, University of Western Ontario, London, ON, Canada.
Kaitlyn R PalmateerDepartment of Microbiology & Immunology, University of Western Ontario, London, ON, Canada.
Jason B WeinbergDepartment of Pediatrics, University of Michigan, Ann Arbor, MI, USA; Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI, USA.
Joe S MymrykDepartment of Microbiology & Immunology, University of Western Ontario, London, ON, Canada; Department of Otolaryngology, University of Western Ontario, London, ON, Canada; Department of Oncology, University of Western Ontario, London, ON, Canada. Electronic address: jmymryk@uwo.ca.

Funding

Modulation of Pediatric Sepsis by Virus PersistenceR01AI184463 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jason Brice Weinberg · 2025 to 2026
$1.4M
Immunoproteasome-Mediated Inflammation in Coronavirus Respiratory InfectionR21AI163720 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WEINBERG, JASON BRICE · 2022 to 2023
$429k
NIAID NIH HHS R01 AI184463NIAID NIH HHS R21 AI163720
6 · The paper itself

Abstract

Human adenoviruses (HAdVs) are ubiquitous human pathogens that infect the respiratory, ocular, and gastrointestinal tissues. Despite the severity of these infections in immunocompromised patients, there are no clinically approved antiviral medications to treat HAdV infections. Over the past decade, many compounds have been found to interfere with different parts of the HAdV replication cycle. One critical barrier to developing a successful HAdV therapy arises if the drug concentration required for antiviral efficacy is clinically unachievable or too toxic for patient use. This problem can be diminished by using a combination of drugs that function synergistically, potentially allowing the use of lower drug concentrations that are clinically achievable and/or exhibit acceptable toxicity profiles. In this exploratory study, we examined the antiviral activity of pairwise combinations of six drugs that have been previously shown to disrupt HAdV replication: ivermectin, digitoxin, deguelin, niclosamide, rosiglitazone, and remdesivir. Combinations of these drugs showed a stronger reduction in HAdV progeny production, protein expression, and genome replication efficiency compared to their individual effects. These experiments serve to illustrate the feasibility and benefits of drug combinations that synergize against HAdV replication.

Indexed as

Adenoviruses, HumanAntiviral AgentsVirus ReplicationAdenovirus Infections, HumanCell LineDrug SynergismDrug Therapy, CombinationHumansAntiviral AgentsAntiviralCombination therapyDeguelinHuman adenovirusIvermectinNiclosamideSynergy

Identifiers

PMID42303049
PMCPMC13371557

What OpenQuestion holds

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LicenceCC BY-NC
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.