Evidence map›Paper›PMID 27631352›Full record

ReviewCornea2016

Translational Immunoimaging and Neuroimaging Demonstrate Corneal Neuroimmune Crosstalk.

Pedram Hamrah, Yashar Seyed-Razavi, Takefumi Yamaguchi

Open access · greenAbstract readReview
In one paragraph

Review in Cornea, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Review
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  11. Review
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  15. Plasmacytoid dendritic cells in the eye.Progress in retinal and eye research · 2021
    Review
  16. Inflammatory basis for dry eye disease flares.Experimental eye research · 2020
    Review
  17. Review
  18. Corneal pain and experimental model development.Progress in retinal and eye research · 2019
    Review
  19. A Novel Murine Model of Radiation Keratopathy.Investigative ophthalmology & visual science · 2018
    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

3 authors at 2 institutions in 2 countries.

Pedram Hamrah*Center of Translational Ocular Immunology, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA; †Boston Image Reading Center, Tufts Medical Center, Tufts University School of Medicine, Boston, MA; and ‡Cornea Service, New England Eye Center, Tufts Medical Center, Tufts University School of Medicine, Boston, MA; Programs in §Immunology; and ¶Neuroscience, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, MA; and ‖Department of Ophthalmology, Ichikawa General Hospital, Tokyo Dental College, Chiba, Japan.
Yashar Seyed-Razavi
Takefumi Yamaguchi
Institute of Neuroimmunology of the Slovak Academy of Sciences · SKTufts Medical Center · US

Funding

The role of plasmacytoid dendritic cells in corneal immunityR01EY022695 · NEI · TUFTS MEDICAL CENTER · PI HAMRAH, PEDRAM · 2013 to 2017
$2.4M
Role of plasmacytoid dendritic cells in corneal nerve health and regenerationR21EY025393 · NEI · TUFTS MEDICAL CENTER · PI HAMRAH, PEDRAM · 2016 to 2017
$454k
NEI NIH HHS R01 EY022695NEI NIH HHS R21 EY025393
6 · The paper itself

Abstract

Corneal immunoimaging and neuroimaging approaches facilitate in vivo analyses of the cornea, including high-resolution imaging of corneal immune cells and nerves. This approach facilitates the analyses of underlying immune and nerve alterations not detected by clinical slit-lamp examination alone. In this review, we describe recent work performed in our translational ocular immunology center with a focus on "bench-to-bedside" and "bedside-to-bench" research. The ability to visualize dendritiform immune cells (DCs) in patients with laser in vivo confocal microscopy (IVCM), recently discovered in the central murine cornea, has allowed us to demonstrate their utility as a potential surrogate biomarker for inflammatory ocular surface diseases. This biomarker for inflammation allows the measurement of therapeutic efficacy of anti-inflammatory drugs and its utility as an endpoint in clinical trials with high interobserver agreement. IVCM image analyses from our studies has demonstrated a significant increase in DC density and size in ocular disease, a positive correlation between DC density and clinical signs and symptoms of disease and pro-inflammatory tear cytokines, and a strong negative correlation between DC density and subbasal nerve density. In conjunction with preclinical research investigating the inflammatory state in a partial or fully denervated cornea, our results indicated that corneal nerves are directly involved in the regulation of homeostasis and immune privilege in the cornea.

Indexed as

AnimalsCorneaDendritic CellsHumansMicroscopy, ConfocalNeuroimagingSignal TransductionTrigeminal Nerve

Identifiers

PMID27631352
PMCPMC5607441
OpenAlexW2519695637

What OpenQuestion holds

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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.