ArticleAntiviral research2026
Drug combination treatment as a strategy for inhibiting human adenovirus replication.
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.
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.
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.
Who cites it
2 citing papers in PubMed.
- Inflammatory marker profiles in immunocompetent hospitalized children with adenovirus infection and association with hospitalization outcomes.Translational pediatrics · 2026Article
- Novel recombinant human adenoviruses: A call for enhanced molecular surveillance, diagnosis, and management in pediatric acute respiratory infections.Pediatric investigation · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
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.
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Registered trials
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.