Evidence map›Paper›PMID 12821466›Full record

ArticleAntimicrobial agents and chemotherapy2003

In vitro activities of benzimidazole D- and L-ribonucleosides against herpesviruses.

Stephanie L Williams, Caroll B Hartline, Nicole L Kushner, Emma A Harden, Deborah J Bidanset, John C Drach, Leroy B Townsend, Mark R Underwood, Karen K Biron, Earl R Kern

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 144 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Anti-CMV therapy, what next? A systematic review.Frontiers in microbiology · 2023
    Review
  16. New Perspectives on Antimicrobial Agents: Maribavir.Antimicrobial agents and chemotherapy · 2022
    Review
  17. Review
  18. Article
  19. Antiviral Drugs Against Herpesviruses.Advances in experimental medicine and biology · 2021
    Article
  20. Review

13 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 1 country.

Stephanie L WilliamsUniversity of Alabama School of Medicine, Birmingham, Alabama 35233, USA.
Caroll B Hartline
Nicole L Kushner
Emma A Harden
Deborah J Bidanset
John C Drach
Leroy B Townsend
Mark R Underwood
Karen K Biron
Earl R Kern
University of Alabama at Birmingham · USResearch Triangle Park Foundation · USUniversity of Michigan–Ann Arbor · US

Funding

NEW HETEROCYCLES AND NUCLEOSIDES AS INHIBITORS OF HCMVP01AI046390 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KERN, EARL R. · 1999 to 2002
$2.3M
IN VITRO ANTIVIRAL SCREEN FOR HERPESVIRUSESN01AI085347 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KERN, EARL R · 1998 to 2000
$764k
NIAID NIH HHS 5-U19-AI46390NIAID NIH HHS N01 AI085347NIAID NIH HHS N01-AI-85347
6 · The paper itself

Abstract

Herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), varicella-zoster virus (VZV), cytomegalovirus (CMV), Epstein-Barr virus (EBV), human herpesvirus 6 (HHV-6), and human herpesvirus 8 (HHV-8) are responsible for a number of clinical manifestations in both normal and immunocompromised individuals. The parent benzimidazole ribonucleosides evaluated in this series, 2-bromo-5,6-dichloro-1-(beta-D-ribofuranosyl)benzimidazole (BDCRB) and maribavir (1263W94), are potent and selective inhibitors of human CMV replication. These nucleosides act by two different mechanisms. BDCRB blocks the processing and maturation of viral DNA, whereas 1263W94 inhibits the viral enzyme pUL97 and interferes with DNA synthesis. In the present study, we have evaluated the in vitro antiviral activity of BDCRB, an analog, GW275175X (175X), and 1263W94 against the replication of HSV-1, HSV-2, VZV, CMV, EBV, HHV-6, and HHV-8. By using various methodologies, significant activity was observed against human CMV and EBV but not against HSV-1, HSV-2, VZV, HHV-6, or HHV-8. Plaque reduction assays performed on a variety of laboratory and clinical isolates of human CMV indicated that all strains, including those resistant to ganciclovir (GCV) and foscarnet, were sensitive to all three benzimidazole ribonucleosides, with mean 50% effective concentration values of about 1 to 5 microM compared to that of GCV at 6 microM. The toxicity of these compounds in tissue culture cells appeared to be similar to that observed with GCV. These results demonstrate that the benzimidazole ribonucleosides are active against human CMV and EBV and suggest that they may be useful for the treatment of infections caused by these herpesviruses.

Indexed as

Antiviral AgentsBenzimidazolesCytomegalovirusHerpesvirus 1, HumanHerpesvirus 2, HumanHerpesvirus 3, HumanHerpesvirus 6, HumanHerpesvirus 8, HumanIn Vitro TechniquesRibonucleosidesVirus ReplicationAntiviral AgentsbenzimidazoleBenzimidazolesRibonucleosides

Identifiers

PMID12821466
PMCPMC161863
OpenAlexW2096682430

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.