Evidence map›Paper›PMID 12388699›Full record

ArticleJournal of virology2002

Use of immunostimulatory sequence-containing oligonucleotides as topical therapy for genital herpes simplex virus type 2 infection.

Richard B Pyles, Debbie Higgins, Claudia Chalk, Anthony Zalar, Joseph Eiden, Carrie Brown, Gary Van Nest, Lawrence R Stanberry

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.9field-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

35 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Expression of toll-like receptors in genital tract tissues from normal and HIV-infected men.American journal of reproductive immunology (New York, N.Y. : 1989) · 2011
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Broad-spectrum drugs against viral agents.International journal of molecular sciences · 2008
    Article
  18. Article
  19. Antiinfective applications of toll-like receptor 9 agonists.Proceedings of the American Thoracic Society · 2007
    Review
  20. 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

8 authors at 3 institutions in 2 countries.

Richard B PylesDepartment of Pediatrics and the Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, Texas 77555, USA. rbpyles@utmb.edu
Debbie Higgins
Claudia Chalk
Anthony Zalar
Joseph Eiden
Carrie Brown
Gary Van Nest
Lawrence R Stanberry
Dynavax Technologies (Germany) · DEThe University of Texas Medical Branch at Galveston · USDynavax Technologies (United States) · US

Funding

TOPICAL MICROBICIDES &BIOLOGY OF VENEREAL PATHOGENSP01AI037940 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI STANBERRY, LAWRENCE R · 1995 to 2003
$3.4M
NIAID NIH HHS P01 AI037940NIAID NIH HHS P01-AI-37940
6 · The paper itself

Abstract

Synthetic oligonucleotides containing CpG motifs in specific sequence contexts have been shown to induce potent immune responses. We have evaluated mucosal administration of two immunostimulatory sequence (ISS)-containing phosphorothioate-stabilized oligonucleotides for antiherpetic efficacy in animal models. The ISS oligonucleotides, suspended in phosphate-buffered saline, were tested in mouse and guinea pig vaginal models of herpes simplex virus type 2 (HSV-2) infection. For comparison, groups of untreated, non-ISS oligonucleotide-treated, and acyclovir-treated animals also were monitored. The results indicated that vaginal epithelial application of ISS (up to 6 h after viral inoculation) with mice lethally challenged with HSV-2 delayed disease onset and reduced the number of animals that developed signs of disease (P = 0.003). ISS application significantly increased survival rates over those of controls (P = 0.0014). The ISS also impacted an established infection in the guinea pig model of HSV-2 disease. A single administration of ISS (21 days after viral inoculation) significantly reduced the frequency and severity of HSV-2 lesions compared to results with non-ISS oligonucleotide-treated and untreated guinea pigs (P < 0.01). HSV-2 is shed from the vaginal cavity of the guinea pig in the absence of lesions, similar to the case with humans. As an additional indication of ISS efficacy, the magnitude of viral shedding also was significantly reduced in ISS-treated animals (P < 0.001). These effects appeared to be immunologically mediated, since ISS had no direct effect on HSV-2 replication in vitro using standard plaque assays. These data suggest that ISS may be useful in the treatment and control of genital herpes in humans.

Indexed as

Administration, IntravaginalAcyclovirAdjuvants, ImmunologicAnimalsAntiviral AgentsBase SequenceChlorocebus aethiopsDisease Models, AnimalFemaleGuinea PigsHerpes GenitalisHerpesvirus 2, HumanHumansMiceMicrobial Sensitivity TestsOligonucleotidesAcyclovirAdjuvants, ImmunologicAntiviral AgentsOligonucleotides

Identifiers

PMID12388699
PMCPMC136753
OpenAlexW2170819284

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.