Evidence map›Paper›PMID 41344864›Full record

ReviewCurrent opinion in infectious diseases2026

Developments in genital herpes: progress in prevention and treatment.

Michelle Collins-Ogle, Betsy C Herold

Abstract readReview
In one paragraph

Review in Current opinion in infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Michelle Collins-OgleDepartment of Pediatrics.
Betsy C HeroldDepartment of Pediatrics.

Funding

Mechanisms Underlying the HIV-HSV-2 SyndemicR01AI134367 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Betsy C. Herold · 2018 to 2026
$4.9M
Optimizing the Generation of Monoclonal Antibodies for Prevention and Treatment of HSV DiseaseR01AI177673 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Betsy C. Herold, Masayuki Kuraoka · 2023 to 2026
$2.4M
The Unexpected Role of TNFRSF14 Signaling in Promoting Antibody-Dependent Cell-Mediated CytotoxicityR01AI187024 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI STEVEN C. ALMO, Betsy C. Herold · 2025 to 2026
$988k
NIAID NIH HHS R01 AI134367NIAID NIH HHS R01 AI177673NIAID NIH HHS R01 AI187024
6 · The paper itself

Abstract

purpose of reviewGenital herpes is a major worldwide public health problem with more than four billion people infected with either herpes simplex virus type 1 (HSV-1) or type 2 (HSV-2). To reduce HSV infections, which greatly impact people of all ages, a thorough understanding of the epidemiology, viral life cycle and correlates of immune protection are essential. This review highlights advances in these areas including new research in vaccine development and potential future strategies for a cure. RECENT

findingsHistorically, HSV-2 was the predominant cause of genital infection, but HSV-1 now accounts for more than half of all new infections worldwide. HSV-1 is less likely than HSV-2 to cause clinical recurrences; however, both can be transmitted perinatally, particularly during primary infection. Neonatal infection may result in disseminated and/or neurologic disease with significant morbidity despite antiviral therapy. Resistance to current antivirals may emerge particularly among immunocompromised patients, highlighting the need for new approaches for treatment and prevention. Prior vaccine trial failures and new research indicate that neutralizing antibodies, long considered the correlate for protection, are not sufficient, and that polyfunctional antibodies with cytolytic activity as well as cellular immune responses will be needed for effective prophylactic and therapeutic vaccines. SUMMARY: HSV infections are usually asymptomatic but the viruses uniformly establish latency with periodic reactivation and the potential for long-term neurologic sequelae. Molecular diagnostics, which has replaced viral culture, has demonstrated that reactivation is more common than previously appreciated. Thus, new approaches to treatment and prevention and ultimately cure are needed.

Indexed as

Antiviral AgentsHerpes GenitalisHerpes Simplex Virus VaccinesHerpesvirus 1, HumanHerpesvirus 2, HumanHumansVaccine DevelopmentAntiviral AgentsHerpes Simplex Virus Vaccinesgene editinggenital herpesmonoclonal antibodiesvaccines

Identifiers

PMID41344864
PMCPMC13070350

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Registered trials

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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.