Evidence map›Paper›PMID 30453079›Full record

ReviewProgress in retinal and eye research2019

Corneal pain and experimental model development.

Tina B McKay, Yashar Seyed-Razavi, Chiara E Ghezzi, Gabriela Dieckmann, Thomas J F Nieland, Dana M Cairns, Rachel E Pollard, Pedram Hamrah, David L Kaplan

Open access · greenAbstract readReview
In one paragraph

Review in Progress in retinal and eye research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 57 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Tina B McKayDepartment of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA, 02155, USA.
Yashar Seyed-RazaviCenter for Translational Ocular Immunology and Cornea Service, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.
Chiara E GhezziDepartment of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA, 02155, USA.
Gabriela DieckmannCenter for Translational Ocular Immunology and Cornea Service, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.
Thomas J F NielandDepartment of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA, 02155, USA.
Dana M CairnsDepartment of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA, 02155, USA.
Rachel E PollardDepartment of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA, 02155, USA.
Pedram HamrahCenter for Translational Ocular Immunology and Cornea Service, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.
David L KaplanDepartment of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA, 02155, USA. Electronic address: david.kaplan@tufts.edu.
Tufts University · US

Funding

Translational Bioreactors - Engineering Complex TissuesP41EB002520 · NIBIB · TUFTS UNIVERSITY MEDFORD · PI KAPLAN, DAVID L. · 2004 to 2018
$16.7M
Mechanisms of Corneal Neuro-Immune CrosstalkR01EY029602 · NEI · UNIVERSITY OF SOUTH FLORIDA · PI Pedram Hamrah · 2018 to 2026
$3.6M
Tissue Regeneration by Biophysical SignalingR01AR055993 · NIAMS · TUFTS UNIVERSITY MEDFORD · PI KAPLAN, DAVID L., LEVIN, MICHAEL · 2010 to 2018
$3.2M
Tissue Engineering Cornea ReplacementsR01EY020856 · NEI · TUFTS UNIVERSITY MEDFORD · PI KAPLAN, DAVID L. · 2010 to 2016
$2.7M
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 EY020856NEI NIH HHS R01 EY022695NEI NIH HHS R01 EY029602NEI NIH HHS R21 EY025393NIAMS NIH HHS R01 AR055993NIBIB NIH HHS P41 EB002520
6 · The paper itself

Abstract

The cornea is a valuable tissue for studying peripheral sensory nerve structure and regeneration due to its avascularity, transparency, and dense innervation. Somatosensory innervation of the cornea serves to identify changes in environmental stimuli at the ocular surface, thereby promoting barrier function to protect the eye against injury or infection. Due to regulatory demands to screen ocular safety of potential chemical exposure, a need remains to develop functional human tissue models to predict ocular damage and pain using in vitro-based systems to increase throughput and minimize animal use. In this review, we summarize the anatomical and functional roles of corneal innervation in propagation of sensory input, corneal neuropathies associated with pain, and the status of current in vivo and in vitro models. Emphasis is placed on tissue engineering approaches to study the human corneal pain response in vitro with integration of proper cell types, controlled microenvironment, and high-throughput readouts to predict pain induction. Further developments in this field will aid in defining molecular signatures to distinguish acute and chronic pain triggers based on the immune response and epithelial, stromal, and neuronal interactions that occur at the ocular surface that lead to functional outcomes in the brain depending on severity and persistence of the stimulus.

Indexed as

AnimalsCorneaCorneal DiseasesEye PainHumansModels, TheoreticalNeuralgiaCorneaDry eyeNeuropeptidesNociceptionPainTissue engineering

Identifiers

PMID30453079
PMCPMC6690397
OpenAlexW2901223717

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.