Evidence map›Paper›PMID 39677756›Full record

ArticlebioRxiv : the preprint server for biology2024

Rebuilding the autoimmune-damaged corneal stroma through topical lubrication.

Yael Efraim, Feeling Yu Ting Chen, Seyyed Vahid Niknezhad, Dylan Pham, Ka Neng Cheong, Luye An, Hanan Sinada, Nancy A McNamara, Sarah M Knox

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

5 · Who and what money

Authors and funding

9 authors.

Yael EfraimProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.
Feeling Yu Ting ChenProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.
Seyyed Vahid NiknezhadProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.
Dylan PhamProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.
Ka Neng CheongProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.
Luye AnProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.
Hanan SinadaProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.
Nancy A McNamaraSchool of Optometry and Vision Science Graduate Program, University of California, Berkeley; Oakland, CA 94720, USA.
Sarah M KnoxProgram in Craniofacial Biology, Department of Cell & Tissue Biology, University of California San Francisco; San Francisco, CA 94143, USA.ORCID 0000-0002-7567-083X

Funding

Defining mechanisms driving dry eye disease progressionR01EY033040 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KNOX, SARAH MONICA, MCNAMARA, NANCY A · 2021 to 2025
$2.1M
Defining the role of the nervous system in aqueous-deficient dry eyeR01EY025980 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KNOX, SARAH MONICA, MCNAMARA, NANCY A · 2015 to 2019
$2.0M
Autonomic regulation of lacrimal stem cellsR01EY027392 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KNOX, SARAH MONICA · 2017 to 2019
$1.2M
NEI NIH HHS R01 EY025980NEI NIH HHS R01 EY027392NEI NIH HHS R01 EY033040
6 · The paper itself

Abstract

Corneal lubrication is the most common treatment for relieving the signs and symptoms of dry eye and is considered to be largely palliative with no regenerative functions. Here we challenge this notion by demonstrating that wetting the desiccated cornea of an aqueous-deficient mouse model with the simplest form of lubrication, a saline-based solution, is sufficient to rescue the severely disrupted collagen-rich architecture of the stroma, the largest corneal compartment that is essential to transparency and vision. At the single cell level we show that stromal keratocytes responsible for maintaining stromal integrity are converted from an inflammatory state into unique reparative cell states by lubrication alone, thus revealing the extensive plasticity of these cells and the regenerative function of lubricating the surface. We further show that the generation of a reparative phenotype is due, in part, to disruption of an IL1β autocrine amplification loop promoting chronic inflammation. Thus, our study uncovers the regenerative potential of topical lubrication in dry eye and represents a paradigm shift in our understanding of its therapeutic impact.

Identifiers

PMID39677756
PMCPMC11642755

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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.