Evidence map›Paper›PMID 37326494›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

Role of IL-27 in HSV-1-Induced Herpetic Stromal Keratitis.

Ferrin Antony, Chetan Pundkar, Maninder Sandey, Amarjit Mishra, Amol Suryawanshi

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Animal models of human herpesvirus infection.Animal models and experimental medicine · 2025
    Review
  2. Article
  3. Review
  4. Review
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 at 1 institution in 1 country.

Ferrin AntonyDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL.ORCID 0000-0001-9269-3614
Chetan PundkarDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL.ORCID 0000-0001-8864-8546
Maninder SandeyDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL.ORCID 0000-0003-4289-3743
Amarjit MishraDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL.
Amol SuryawanshiDepartment of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL.ORCID 0000-0001-5031-5818
Auburn University · US

Funding

Targeting anti-viral and anti-inflammatory responses during ocular HSV-1 infection to prevent vision impairment.R15EY035057 · NEI · AUBURN UNIVERSITY AT AUBURN · PI RAMAPURAM, JAYACHANDRA B · 2023 to 2023
$453k
Th1/Th17 Immune Regulation in Severe Allergic AsthmaR03AI153794 · NIAID · AUBURN UNIVERSITY AT AUBURN · PI MITRA, AMIT K, SURYAWANSHI, AMOL · 2021 to 2022
$149k
NEI NIH HHS R15 EY035057NIAID NIH HHS R03 AI153794
6 · The paper itself

Abstract

Herpetic stromal keratitis (HSK) is a painful and vision-impairing disease caused by recurrent HSV-1 infection of the cornea. The virus replication in the corneal epithelium and associated inflammation play a dominant role in HSK progression. Current HSK treatments targeting inflammation or virus replication are partially effective and promote HSV-1 latency, and long-term use can cause side effects. Thus, understanding molecular and cellular events that control HSV-1 replication and inflammation is crucial for developing novel HSK therapies. In this study, we report that ocular HSV-1 infection induces the expression of IL-27, a pleiotropic immunoregulatory cytokine. Our data indicate that HSV-1 infection stimulates IL-27 production by macrophages. Using a primary corneal HSV-1 infection mouse model and IL-27 receptor knockout mice, we show that IL-27 plays a critical role in controlling HSV-1 shedding from the cornea, the optimum induction of effector CD4+ T cell responses, and limiting HSK progression. Using in vitro bone marrow-derived macrophages, we show that IL-27 plays an antiviral role by regulating macrophage-mediated HSV-1 killing, IFN-β production, and IFN-stimulated gene expression after HSV-1 infection. Furthermore, we report that IL-27 is critical for macrophage survival, Ag uptake, and the expression of costimulatory molecules involved in the optimum induction of effector T cell responses. Our results indicate that IL-27 promotes endogenous antiviral and anti-inflammatory responses and represents a promising target for suppressing HSK progression.

Indexed as

CorneaInterleukinsKeratitis, HerpeticAnimalsFemaleHerpesvirus 1, HumanImmunity, InnateInterferon-betaMacrophagesMaleMiceMice, KnockoutTh1 CellsVirus SheddingIl27 protein, mouseInterferon-betaInterleukins

Identifiers

PMID37326494
PMCPMC10495105
OpenAlexW4380870737

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.