Evidence map›Paper›PMID 42189879›Full record

ArticlePLoS pathogens2026

Partial or complete blocking of gD binding to HVEM affects primary and latent HSV-1 infection as well as eye disease in HSV-1 infected mice.

Deepak Arya, Ujjaldeep Jaggi, Jay J Oh, Shaohui Wang, Homayon Ghiasi

Abstract read
In one paragraph

Article in PLoS pathogens, 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

5 authors.

Deepak AryaDepartment of Surgery, Center for Neurobiology and Vaccine Development, Ophthalmology Research, Cedars-Sinai Medical Center, Cedars-Sinai Health Sciences University, Los Angeles, California, United States of America.
Ujjaldeep JaggiDepartment of Surgery, Center for Neurobiology and Vaccine Development, Ophthalmology Research, Cedars-Sinai Medical Center, Cedars-Sinai Health Sciences University, Los Angeles, California, United States of America.
Jay J OhDepartment of Surgery, Center for Neurobiology and Vaccine Development, Ophthalmology Research, Cedars-Sinai Medical Center, Cedars-Sinai Health Sciences University, Los Angeles, California, United States of America.
Shaohui WangDepartment of Surgery, Center for Neurobiology and Vaccine Development, Ophthalmology Research, Cedars-Sinai Medical Center, Cedars-Sinai Health Sciences University, Los Angeles, California, United States of America.
Homayon GhiasiDepartment of Surgery, Center for Neurobiology and Vaccine Development, Ophthalmology Research, Cedars-Sinai Medical Center, Cedars-Sinai Health Sciences University, Los Angeles, California, United States of America.ORCID https://orcid.org/0000-0003-3291-1995

Funding

Therapeutic control of HSK by CD80R01EY026944 · NEI · CEDARS-SINAI MEDICAL CENTER · PI GHIASI, HOMAYON · 2016 to 2025
$3.9M
Ocular HSV: Mechanism of virus reactivationR01EY029160 · NEI · CEDARS-SINAI MEDICAL CENTER · PI HOMAYON GHIASI · 2018 to 2026
$3.4M
Role of type 1 IFN in eye infectionR01EY033574 · NEI · CEDARS-SINAI MEDICAL CENTER · PI HOMAYON GHIASI · 2023 to 2026
$1.9M
NEI NIH HHS R01 EY026944NEI NIH HHS R01 EY029160NEI NIH HHS R01 EY033574
6 · The paper itself

Abstract

Herpes simplex virus type 1 (HSV-1) glycoprotein D (gD) engages herpesvirus entry mediator (HVEM) and other cellular receptors to mediate efficient viral attachment. We recently identified gD amino acids (aa) Q27-T29 as critical to completely block gD binding to HVEM, while the single Q27P mutation in gD reduced its binding to HVEM by approximately 80%. Thus, we constructed two mutant viruses: one with a single gD aa mutation (v27) and the other with three gD aa mutations (v27-29) in the HSV-1 strain GFP-McKrae background. These mutant viruses clearly demonstrated the consequences of disrupting gD binding to HVEM, which reduced HVEM expression and altered the expression of other receptors. To determine whether these mutations also affected viral replication, ocular disease severity, latency levels, and reactivation kinetics, mice were ocularly infected with WT, v27, or v27-29 viruses. Both mutant viruses exhibited significantly reduced viral replication in tears compared with the WT virus, even after corneal scarification. The v27-29 virus showed a greater reduction in viral replication than the v27 virus. Mice infected with both mutant viruses had significantly lower levels of eye disease, latency, and T cell exhaustion than in WT virus-infected mice. In the absence of scarification, significantly fewer trigeminal ganglia (TG) were reactivated by mutant viruses than by the WT virus. In contrast, after scarification, all TG from WT-, v27-, and v27-29-infected mice were reactivated, and the time to reactivate was similar between the two mutant viruses, but reactivation was significantly less delayed than in WT-infected mice. Together, these findings demonstrate that disrupting gD-HVEM binding reduces viral virulence and limits latency, reactivation, and T cell exhaustion. Thus, the Q27-T29 region of gD is a critical determinant of infection dynamics and a potential therapeutic or vaccine target.

Indexed as

Herpes SimplexHerpesvirus 1, HumanReceptors, Tumor Necrosis Factor, Member 14Viral Envelope ProteinsAnimalsFemaleHumansKeratitis, HerpeticMiceMutationProtein BindingVirus LatencyVirus Replicationglycoprotein D, Human herpesvirus 1glycoprotein gD, herpes simplex virus type 1Receptors, Tumor Necrosis Factor, Member 14Tnfrsf14 protein, mouseViral Envelope Proteins

Identifiers

PMID42189879
PMCPMC13221150

What OpenQuestion holds

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LicenceCC BY
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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.