Evidence map›Paper›PMID 23536670›Full record

ArticleJournal of virology2013

Griffithsin protects mice from genital herpes by preventing cell-to-cell spread.

Briana Nixon, Martha Stefanidou, Pedro M M Mesquita, Esra Fakioglu, Theodore Segarra, Lisa Rohan, William Halford, Kenneth E Palmer, Betsy C Herold

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
6.1field-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

77 citing papers in PubMed, 114 citations in OpenAlex.

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  13. An algal lectin griffithsin inhibits Hantaan virus infectionFrontiers in cellular and infection microbiology · 2022
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17 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

9 authors at 4 institutions in 1 country.

Briana NixonDepartment of Pediatrics, Albert Einstein College of Medicine, Bronx, New York, USA.
Martha Stefanidou
Pedro M M Mesquita
Esra Fakioglu
Theodore Segarra
Lisa Rohan
William Halford
Kenneth E Palmer
Betsy C Herold
Albert Einstein College of Medicine · USOwensboro Health · USSouthern Illinois University School of Medicine · USUniversity of Pittsburgh · US

Funding

Immunology/Pathology CoreP30AI051519 · NIAID · YESHIVA UNIVERSITY · PI GOLDSTEIN, HARRIS · 2003 to 2013
$18.6M
Sustained Intravaginal Delivery Technologies Against HIV and HSVU19AI076980 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI MITCHNICK, MARK · 2009 to 2012
$10.1M
Antiviral lectins as microbicidesR01AI076169 · NIAID · UNIVERSITY OF LOUISVILLE · PI PALMER, KENNETH E · 2008 to 2011
$2.3M
Development of an effective genital herpes vaccineR21AI081072 · NIAID · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI HALFORD, WILLIAM P · 2009 to 2010
$504k
NIAID NIH HHS AI-051519NIAID NIH HHS P30 AI051519NIAID NIH HHS R01 AI076169NIAID NIH HHS R01AI076169NIAID NIH HHS R21 AI081072NIAID NIH HHS R21AI81072NIAID NIH HHS U19 AI076980NIAID NIH HHS U19AI076980
6 · The paper itself

Abstract

Griffithsin, which binds N-linked glycans on gp120 to prevent HIV entry, has the most potent HIV-1 inhibitory activity described for any antiviral lectin and is being developed for topical preexposure prophylaxis. The current studies were designed to further assess its potential by exploring its activity against herpes simplex virus 2 (HSV-2), a cofactor for HIV acquisition, in vitro and in a murine model. Safety was evaluated by examining its impact on epithelial barrier integrity in polarized cultures and testing whether repeated intravaginal dosing potentiates the susceptibility of mice to genital herpes. Griffithsin displayed modest inhibitory activity against HSV-2 if present during viral entry but completely blocked plaque formation if present postentry, reduced plaque size, and prevented cell-to-cell spread. These in vitro findings translated to significant protection against genital herpes in mice treated with 0.1% griffithsin gel. Griffithsin, but not placebo gel, prevented viral spread (visualized with a luciferase-expressing virus), significantly reduced disease scores, and resulted in greater survival (P < 0.05, log rank test). Protection persisted when HSV-2 was introduced in seminal plasma. Although griffithsin triggered a small decline in transepithelial electrical resistance in polarized cultures, this did not translate to any significant increase in the ability of HIV to migrate from the apical to the basolateral chamber nor to an increase in susceptibility to HSV-2 in mice treated with griffithsin gel for 7 days. These findings demonstrate that griffithsin inhibits HSV-2 by a unique mechanism of blocking cell-to-cell spread and support its further development for HIV and HSV-2 prevention.

Indexed as

AnimalsAntiviral AgentsFemaleHerpes GenitalisHerpesvirus 2, HumanHumansMiceMice, Inbred BALB CPlant LectinsVirus InternalizationAntiviral Agentsgriffithsin protein, GriffithsiaPlant Lectins

Identifiers

PMID23536670
PMCPMC3648100
OpenAlexW2150924565

What Socratic 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 Socratic graph.