Evidence map›Paper›PMID 32272093›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2020

Vaccines to prevent genital herpes.

Kevin Egan, Lauren M Hook, Philip LaTourette, Angela Desmond, Sita Awasthi, Harvey M Friedman

Open access · greenAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  7. Therapeutic vaccines for herpesviruses.The Journal of clinical investigation · 2024
    Review
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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

6 authors at 2 institutions in 1 country.

Kevin EganInfectious Disease Division, Department of Medicine, Perelman School of Medicine, Philadelphia, PA.
Lauren M HookInfectious Disease Division, Department of Medicine, Perelman School of Medicine, Philadelphia, PA.
Philip LaTouretteUniversity Laboratory Animal Resources, Philadelphia, PA; Department of Pathobiology, School of Veterinary Medicine, Philadelphia, PA.
Angela DesmondInfectious Disease Division, Department of Pediatrics, The Children's Hospital of Philadelphia; University of Pennsylvania, Philadelphia, Pennsylvania.
Sita AwasthiInfectious Disease Division, Department of Medicine, Perelman School of Medicine, Philadelphia, PA.
Harvey M FriedmanInfectious Disease Division, Department of Medicine, Perelman School of Medicine, Philadelphia, PA. Electronic address: hfriedma@pennmedicine.upenn.edu.
University of Pennsylvania · USChildren's Hospital of Philadelphia · US

Funding

Nucleoside-modified mRNA vaccine for prevention and treatment of genital herpesR01AI139618 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Harvey Michael Friedman · 2019 to 2026
$6.4M
TRAINING IN NEUROVIROLOGY AND NEUROIMMUNOLOGYT32NS007180 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI WEISS, SUSAN R · 1985 to 2018
$2.8M
Combined Adult and Pediatric Infectious Disease Postdoctoral Training GrantT32AI118684 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Rahul Manu Kohli, Audrey Ragan Odom John · 2016 to 2026
$2.3M
NIAID NIH HHS R01 AI139618NIAID NIH HHS T32 AI118684NINDS NIH HHS T32 NS007180
6 · The paper itself

Abstract

Genital herpes increases the risk of acquiring and transmitting Human Immunodeficiency Virus (HIV), is a source of anxiety for many about transmitting infection to intimate partners, and is life-threatening to newborns. A vaccine that prevents genital herpes infection is a high public health priority. An ideal vaccine will prevent both genital lesions and asymptomatic subclinical infection to reduce the risk of inadvertent transmission to partners, will be effective against genital herpes caused by herpes simplex virus types 1 and 2 (HSV-1, HSV-2), and will protect against neonatal herpes. Three phase 3 human trials were performed over the past 20 years that used HSV-2 glycoproteins essential for virus entry as immunogens. None achieved its primary endpoint, although each was partially successful in either delaying onset of infection or protecting a subset of female subjects that were HSV-1 and HSV-2 uninfected against HSV-1 genital infection. The success of future vaccine candidates may depend on improving the predictive value of animal models by requiring vaccines to achieve near-perfect protection in these models and by using the models to better define immune correlates of protection. Many vaccine candidates are under development, including DNA, modified mRNA, protein subunit, killed virus, and attenuated live virus vaccines. Lessons learned from prior vaccine studies and select candidate vaccines are discussed, including a trivalent nucleoside-modified mRNA vaccine that our laboratory is pursuing. We are optimistic that an effective vaccine for prevention of genital herpes will emerge in this decade.

Indexed as

AnimalsAntibodies, ViralClinical Trials as TopicDisease Models, AnimalHerpes GenitalisHumansImmune EvasionViral VaccinesAntibodies, ViralViral Vaccines

Identifiers

PMID32272093
PMCPMC7293938
OpenAlexW3011466771

What OpenQuestion holds

Textmetadata
LicenceTDM
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.