Evidence map›Paper›PMID 12388683›Full record

ArticleJournal of virology2002

Mandelic acid condensation polymer: novel candidate microbicide for prevention of human immunodeficiency virus and herpes simplex virus entry.

B C Herold, I Scordi-Bello, N Cheshenko, D Marcellino, M Dzuzelewski, F Francois, R Morin, V Mas Casullo, R A Anderson, C Chany and 3 more

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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-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

26 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Antiviral strategies targeting herpesviruses.Journal of virus eradication · 2021
    Review
  8. Review
  9. Article
  10. Article
  11. Drug delivery strategies and systems for HIV/AIDS pre-exposure prophylaxis and treatment.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  12. Review
  13. Cutaneous infections and infestations: new therapies.The Journal of clinical and aesthetic dermatology · 2011
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

13 authors at 3 institutions in 1 country.

B C HeroldDepartments of Pediatrics, Mount Sinai School of Medicine, New York, New York 10029, USA. betsy.herold@mssn.edu
I Scordi-Bello
N Cheshenko
D Marcellino
M Dzuzelewski
F Francois
R Morin
V Mas Casullo
R A Anderson
C Chany
D P Waller
L J D Zaneveld
M E Klotman
Icahn School of Medicine at Mount Sinai · USRush University · USUniversity of Illinois Chicago · US

Funding

Mechanism of SAMMA against HSV: key cofactor for HIVP01HD041763 · NICHD · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI KLOTMAN, MARY E. · 2001 to 2004
$4.6M
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 AI37940NIAID NIH HHS P01 AI037940NICHD NIH HHS HD41763NICHD NIH HHS P01 HD041763
6 · The paper itself

Abstract

Presently marketed vaginal barrier methods are cytotoxic and damaging to the vaginal epithelium and natural vaginal flora when used frequently. Novel noncytotoxic agents are needed to protect men and women from sexually transmitted diseases. One novel candidate is a mandelic acid condensation polymer, designated SAMMA. The spectrum and mechanism of antiviral activity were explored using clinical isolates and laboratory-adapted strains of human immunodeficiency virus (HIV) and herpes simplex virus (HSV). SAMMA is highly effective against all CCR5 and CXCR4 isolates of HIV in primary human macrophages and peripheral blood mononuclear cells. SAMMA also inhibits infection of cervical epithelial cells by HSV. Moreover, it exhibits little or no cytotoxicity and has an excellent selectivity index. SAMMA, although not a sulfonated or sulfated polymer, blocks the binding of HIV and HSV to cells by targeting the envelope glycoproteins gp120 and gB-2, respectively, and also inhibits HSV entry postattachment. SAMMA is an excellent, structurally novel candidate microbicide that warrants further preclinical evaluation.

Indexed as

Antiviral AgentsCell LineHerpes SimplexHIV-1HIV InfectionsHumansLeukocytes, MononuclearMacrophagesMandelic AcidsMicrobial Sensitivity TestsPolymersSimplexvirusAntiviral Agentsmandelic acidMandelic AcidsPolymers

Identifiers

PMID12388683
PMCPMC136750
OpenAlexW2131149359

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.