Evidence map›Paper›PMID 11257039›Full record

ArticleAntimicrobial agents and chemotherapy2001

Antiviral activity of lovastatin against respiratory syncytial virus in vivo and in vitro.

T L Gower, B S Graham

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 129 citations in OpenAlex.

  1. Trial
  2. Article
  3. Impact of protein prenylation inhibition onJournal of bacteriology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. The role of lovastatin in the attenuation of COVID-19.International immunopharmacology · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. New Approaches to the Prevention and Treatment of Viral Diseases.Archivum immunologiae et therapiae experimentalis · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

2 authors at 2 institutions in 2 countries.

T L GowerDepartment of Microbiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
B S Graham
Bipar · FRVanderbilt University · US

Funding

RSV-INDUCED PATTERNS OF CYTOKINE EXPRESSION AND DISEASER01AI033933 · NIAID · VANDERBILT UNIVERSITY · PI TANG, YI-WEI · 1994 to 2003
$1.1M
The Role Of Rhoa In Rsv Pathogenesis And MorphogenesisZ01AI005030 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI GRAHAM, BARNEY SCOTT · 2002 to 2007
$775k
NIAID NIH HHS R01 AI033933NIAID NIH HHS R01-AI-33933
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is an important human pathogen that can cause severe and life-threatening respiratory infections in infants and immunocompromised adults. We have recently shown that the RSV F glycoprotein, which mediates viral fusion, binds to RhoA. One of the steps in RhoA activation involves isoprenylation at the carboxy terminus of the protein by geranylgeranyltransferase. This modification allows RhoA to be attached to phosphatidyl serine on the inner leaflet of the plasma membrane. Treatment of mice with lovastatin, a drug that inhibits prenylation pathways in the cell by directly inhibiting hydroxymethylglutaryl coenzyme A reductase, diminishes RSV but not vaccinia virus replication when administered up to 24 h after RSV infection and decreases virus-induced weight loss and illness in mice. The inhibition of replication is not likely due to the inhibition of cholesterol biosynthesis, since gemfibrozil, another cholesterol-lowering agent, did not affect virus replication and serum cholesterol levels were not significantly lowered by lovastatin within the time frame of the experiment. Lovastatin also reduces cell-to-cell fusion in cell culture and eliminates RSV replication in HEp-2 cells. These data indicate that lovastatin, more specific isoprenylation inhibitors, or other pharmacological approaches for preventing RhoA membrane localization should be considered for evaluation as a preventive antiviral therapy for selected groups of patients at high risk for severe RSV disease, such as the institutionalized elderly and bone marrow or lung transplant recipients.

Indexed as

Acute DiseaseAnimalsAntiviral AgentsCell FusionCell LineCholesterolFemaleLovastatinMiceMice, Inbred BALB CMice, Inbred C57BLMicrobial Sensitivity TestsRespiratory Syncytial Virus InfectionsVirus ReplicationAntiviral AgentsCholesterolLovastatin

Identifiers

PMID11257039
PMCPMC90448
OpenAlexW2051761287

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.