Evidence map›Paper›PMID 42158934›Full record

ArticlebioRxiv : the preprint server for biology2026

Immunization with Herpes Simplex Virus Nanoparticles Targeting Both Attachment and Fusion Protect Against Infection.

Dawid Maciorowski, Alexander C Vostal, Wei Bu, Isabella S Pytel, Sophia Antonioli-Schmit, Jianghai Zhu, Forrest H Hoyt, Haotian Lei, Guangping Liu, Kristen Kaiser and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Dawid MaciorowskiLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.ORCID 0000-0002-4163-9535
Alexander C VostalLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.ORCID 0000-0002-5618-6225
Wei BuLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.
Isabella S PytelLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.
Sophia Antonioli-SchmitResearch Technologies Branch, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Hamilton MT/Bethesda MD, USA.
Jianghai ZhuResearch Technologies Branch, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Hamilton MT/Bethesda MD, USA.
Forrest H HoytResearch Technologies Branch, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Hamilton MT/Bethesda MD, USA.
Haotian LeiResearch Technologies Branch, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Hamilton MT/Bethesda MD, USA.
Guangping LiuLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.
Kristen KaiserExperimental Primate Virology Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Poolesville MD, USA.
Richard HerbertExperimental Primate Virology Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Poolesville MD, USA.
Kennichi C DowdellLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.
John T SchillerCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda MD, USA.
Kening WangLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.
Mark R HowarthDepartment of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge, UK.ORCID 0000-0001-8870-7147
Jeffrey I CohenLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda MD, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herpes simplex virus 2 (HSV-2) is associated with genital ulcers, neonatal encephalitis, increased risk of HIV infection, and dementia. There is no licensed HSV-2 vaccine. We developed nanoparticles displaying the HSV-2 attachment protein gD and fusion mediation protein complex gH/gL. Immunization of mice and non-human primates elicited high levels of neutralizing antibodies. Vaccination conferred robust protection in mice, preventing disease and nearly eliminating infection and shedding following HSV-2 challenge. While gD induced high neutralizing antibody titers, gH/gL contributed substantially to protection despite lower neutralization titers. Instead, gH/gL immunization generated strong fusion-blocking responses which were an important correlate of protection, showing that standard neutralization assays incompletely capture the importance of fusion-blocking activity. These findings demonstrate that targeting both HSV-2 attachment and fusion elicit complementary mechanisms for protection from infection and that neutralizing antibody alone may be insufficient for protection. Overall, these results present an innovative strategy for an HSV-2 vaccine.

Identifiers

PMID42158934
PMCPMC13182188

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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.