Evidence map›Paper›PMID 40573384›Full record

ReviewViruses2025

Insights into the Currently Available Drugs and Investigational Compounds Against RSV with a Focus on Their Drug-Resistance Profiles.

Alessia Magnapera, Anna Riccio, Antonio Curcio, Caterina Tramontozzi, Lorenzo Piermatteo, Stefano D'Anna, Stefano Alcaro, Claudia Alteri, Simone La Frazia, Anna Artese and 2 more

Abstract readReview
In one paragraph

Review in Viruses, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

12 authors.

Alessia MagnaperaDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID 0009-0000-4659-0219
Anna RiccioDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-1140-1366
Antonio CurcioDepartment of Health Science, Magna Graecia University, 88100 Catanzaro, Italy.ORCID 0009-0005-6818-5325
Caterina TramontozziDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.
Lorenzo PiermatteoDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-3500-0858
Stefano D'AnnaDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID 0009-0003-9334-8582
Stefano AlcaroDepartment of Health Science, Magna Graecia University, 88100 Catanzaro, Italy.ORCID 0000-0002-0437-358X
Claudia AlteriDepartment of Oncology and Hemato-Oncology, University of Milan, 20122 Milan, Italy.
Simone La FraziaDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.
Anna ArteseDepartment of Health Science, Magna Graecia University, 88100 Catanzaro, Italy.ORCID 0000-0002-4638-7760
Romina SalpiniDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-2488-2082
Valentina SvicherDepartment of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is a leading cause of severe respiratory illness in infants, young children, as well as elderly and immunocompromised patients worldwide. RSV is classified into two major subtypes, RSV-A and RSV-B, and remains the most frequently detected pathogen in infants hospitalized with acute respiratory infections. Recent advances have brought both passive and active immunization strategies, including FDA-approved vaccines for older adults and pregnant women and new monoclonal antibodies (mAbs) for infant protection. Although significant progress has been made, the need remains for improved antiviral treatments, particularly for vulnerable infants and immunocompromised patients. Recent studies have identified multiple RSV mutations that confer resistance to current treatments. These mutations, detected in both in vitro studies and clinical isolates, often complicate therapeutic outcomes, underscoring the need for updated and effective management strategies. In this context, evaluating protein flexibility through tools like DisoMine provides insight into how specific mutations impact structural dynamics at binding sites, thus affecting ligand affinity. This review aims to synthesize these aspects, offering a comprehensive insight into ongoing efforts to counteract RSV and address the evolving challenge of drug resistance.

Indexed as

Antiviral AgentsDrug Resistance, ViralDrugs, InvestigationalRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsAnimalsHumansMutationAntiviral AgentsDrugs, Investigationaldrug resistancemutationsnovel drugsRSVstructural dynamics

Identifiers

PMID40573384
PMCPMC12197531

What OpenQuestion holds

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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.