Evidence map›Paper›PMID 42796671›Full record

ReviewPathogens (Basel, Switzerland)2026

Target-Based Antiviral Drug Development Against Human Respiratory Viruses.

Subodh Kumar Samrat, Gauri Srivastava, Ran Zhang, Zhong Li, Hongmin Li

Abstract readReview
In one paragraph

Review in Pathogens (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Subodh Kumar SamratDepartment of Pharmacology and Toxicology, R. Ken Coit College of Pharmacy, The University of Arizona, 1703 E Mabel St, Tucson, AZ 85721, USA.
Gauri SrivastavaDepartment of Pharmacology and Toxicology, R. Ken Coit College of Pharmacy, The University of Arizona, 1703 E Mabel St, Tucson, AZ 85721, USA.
Ran ZhangDepartment of Pharmacology and Toxicology, R. Ken Coit College of Pharmacy, The University of Arizona, 1703 E Mabel St, Tucson, AZ 85721, USA.ORCID 0000-0001-7233-1798
Zhong LiDepartment of Pharmacology and Toxicology, R. Ken Coit College of Pharmacy, The University of Arizona, 1703 E Mabel St, Tucson, AZ 85721, USA.
Hongmin LiDepartment of Pharmacology and Toxicology, R. Ken Coit College of Pharmacy, The University of Arizona, 1703 E Mabel St, Tucson, AZ 85721, USA.

Funding

Development of Inhibitors Targeting Flavivirus MethyltransferaseR01AI175435 · NIAID · UNIVERSITY OF ARIZONA · PI HONGMIN LI · 2023 to 2026
$3.1M
Development of Inhibitors Against SARS CoV-2 NSP16 MethyltransferaseR41AI177149 · NIAID · LYCHEE BIOSCIENCE LLC · PI LI, HONGMIN · 2024 to 2025
$600k
NIAID NIH HHS R01 AI175435NIAID NIH HHS R41 AI177149University of Arizona AI177149 and AI175435
6 · The paper itself

Abstract

Human respiratory viruses represent a major global health burden, causing millions of severe infections and deaths annually. Despite the central role of vaccines in prevention, their limitations, such as incomplete coverage, waning immunity, and vulnerability to viral evolution, underscore the urgent need for effective antiviral therapeutics. This review examines the principles and applications of target-based antiviral drug development against human respiratory viruses, emphasizing the identification and exploitation of conserved viral and host targets. Key viral proteins, including RNA-dependent RNA polymerases, proteases, and fusion glycoproteins, are analyzed across major virus families such as coronaviruses, paramyxoviruses, and adenoviruses, highlighting their structural features, functional constraints, and therapeutic potential. We further explore the integration of high-throughput screening and rational drug design, supported by advances in structural biology, cryo-electron microscopy, and computational approaches, including artificial intelligence-driven drug discovery. These methodologies collectively enhance the precision and efficiency of antiviral development. However, significant challenges remain, particularly the conflict between viral mutation and target conservation, the rapid emergence of drug resistance, and the safety limitations of host-targeted therapies. Finally, we discuss emerging strategies to overcome these barriers, including combination therapies and the development of broad-spectrum antivirals targeting conserved molecular mechanisms. This paper highlights a framework for the rational design of durable antiviral interventions capable of addressing both existing and emerging respiratory viral threats.

Indexed as

Antiviral AgentsDrug DevelopmentRespiratory Tract InfectionsCoronavirusDrug DesignDrug DiscoveryHumansViral ProteinsAntiviral AgentsViral Proteinsadenovirusantiviral developmentantiviral reviewcoronavirusdrug discoveryhuman parainfluenza virus (hPIV)measlesrespiratory syncytial virus (RSV)respiratory virusesviral replication

Identifiers

PMID42796671
PMCPMC13610257

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.