Evidence map›Paper›PMID 27497323›Full record

ArticleThe American journal of pathology2016

IL-6 Contributes to Corneal Nerve Degeneration after Herpes Simplex Virus Type I Infection.

Ana J Chucair-Elliott, Jeremy Jinkins, Meghan M Carr, Daniel J J Carr

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Meeting the Challenge of Controlling Viral Immunopathology.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Regenerative therapy for the Cornea.Progress in retinal and eye research · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Role of theMolecular vision · 2020
    Article
  20. 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

4 authors at 1 institution in 1 country.

Ana J Chucair-ElliottDepartment of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma. Electronic address: ana-chucair@ouhsc.edu.
Jeremy JinkinsDepartment of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Meghan M CarrDepartment of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Daniel J J CarrDepartment of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma; Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
University of Oklahoma Health Sciences Center · US

Funding

P30-CENTER CORE GRANT FOR VISION RESEARCHP30EY021725 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Michelle C Callegan, MICHAEL H ELLIOTT · 2011 to 2026
$10.5M
Corneal Lymphatics & Adaptive ImmunityR01EY021238 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CARR, DANIEL J · 2011 to 2020
$3.6M
NEI NIH HHS P30 EY021725NEI NIH HHS R01 EY021238
6 · The paper itself

Abstract

Herpes simplex virus type 1 (HSV-1) is a leading cause of neurotrophic keratitis characterized by decreased corneal sensation because of damage to the corneal sensory fibers. We and others have reported regression of corneal nerves during acute HSV-1 infection. To determine whether denervation is caused directly by the virus or indirectly by the elicited immune response, mice were infected with HSV-1 and topically treated with dexamethasone (DEX) or control eye drops. Corneal sensitivity was measured using a Cochet-Bonnet esthesiometer and nerve network structure via immunohistochemistry. Corneas were assessed for viral content by plaque assay, leukocyte influx by flow cytometry, and content of chemokines and inflammatory cytokines by suspension array. DEX significantly preserved corneal nerve structure and sensitivity on infection. DEX reduced myeloid and T-cell populations in the cornea and did not affect viral contents at 4 and 8 days post infection. The elevated protein contents of chemokines and inflammatory cytokines on infection were greatly suppressed by DEX. Subconjunctival delivery of neutralizing antibody against IL-6 to infected mice resulted in partial preservation of corneal nerve structure and sensitivity. Our study supports a role for the immune response, but not local virus replication in the development of HSV-1-induced neurotrophic keratitis. IL-6 is one of the factors produced by the elicited inflammatory response to HSV-1 infection contributing to nerve regression.

Indexed as

AnimalsAntibodies, NeutralizingAnti-Inflammatory AgentsChemokinesCorneaCorneal DiseasesCytokinesDexamethasoneHerpesvirus 1, HumanInterleukin-6Keratitis, HerpeticMiceMyeloid CellsNerve DegenerationT-LymphocytesAntibodies, NeutralizingAnti-Inflammatory AgentsChemokinesCytokinesDexamethasoneInterleukin-6interleukin-6, mouse

Identifiers

PMID27497323
PMCPMC5222975
OpenAlexW2487091400

What OpenQuestion holds

Textmetadata
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.