Evidence map›Paper›PMID 42185525›Full record

ArticleCommunications medicine2026

Mathematical modeling of the population-level impact of hypothetical herpes simplex virus type 2 curative therapy.

Houssein H Ayoub, Keith R Jerome, Hiam Chemaitelly, Anna Wald, Laith J Abu-Raddad

Abstract read
In one paragraph

Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Houssein H AyoubMathematics Program, Department of Mathematics and Statistics, College of Arts and Sciences, Qatar University, Doha, Qatar. hayoub@qu.edu.qa.ORCID http://orcid.org/0000-0003-2512-6657
Keith R JeromeVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID http://orcid.org/0000-0002-8212-3789
Hiam ChemaitellyInfectious Disease Epidemiology Group, Weill Cornell Medicine-Qatar, Cornell University, Doha, Qatar.ORCID http://orcid.org/0000-0002-8756-6968
Anna WaldVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID http://orcid.org/0000-0003-3486-6438
Laith J Abu-RaddadInfectious Disease Epidemiology Group, Weill Cornell Medicine-Qatar, Cornell University, Doha, Qatar. lja2002@qatar-med.cornell.edu.ORCID http://orcid.org/0000-0003-0790-0506

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHerpes simplex virus type 2 (HSV-2) infection is a prevalent lifelong infection and the leading cause of genital ulcer disease (GUD), yet no vaccines or curative interventions are currently available. Emerging curative approaches have demonstrated proof-of-concept efficacy in preclinical studies, but their potential population-level impact remains unknown. This study assessed the potential impact of curative therapy on HSV-2 disease burden and transmission.

methodsA dynamic HSV-2 transmission model was developed for the United States and calibrated to prevalence estimates from the National Health and Nutrition Examination Surveys. Curative therapy was assumed to be introduced in 2030 and scaled to 20%, 50%, or 80% coverage by 2040 under two scenarios: (i) treatment of symptomatic individuals only and (ii) treatment of all individuals with HSV-2 infection.

resultsHere we show that, by 2050, at 80% coverage, curative therapy for symptomatic individuals reduces the number of 15-49-year-olds with GUD and GUD days by 86.7% and 86.2%, respectively, and decreases the incidence rate and annual new infections by 54.0% and 51.7%, averting 5.4 million cumulative infections. The numbers needed to treat to avert one prevalent or incident symptomatic HSV-2 infection, one incident HSV-2 infection, and one year of GUD days are 0.90, 3.4, and 0.61, respectively.

conclusionsCurative therapy could substantially reduce HSV-2 incidence and recurrent GUD, yielding population-level benefits beyond individual cure.

Identifiers

PMID42185525
PMCPMC13483040

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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.