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Type 1–type 2 interferon imbalance in dry eye disease

PURPOSE: Dry eye disease (DED) is characterized by altered ocular surface proinflammatory and antiinflammatory factors. Interferons (IFNs) are a class of pleiotropic cytokines well known for their antimicrobial, inflammatory, and immunomodulatory roles. Hence, this study investigates the ocular surf...

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Autores principales: Panigrahi, Trailokyanath, D’Souza, Sharon, Suresh Babu, Vishnu, Dickman, Mor M, Nuijts, Rudy M M A, Sethu, Swaminathan, Shetty, Rohit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276729/
https://www.ncbi.nlm.nih.gov/pubmed/37026295
http://dx.doi.org/10.4103/IJO.IJO_2842_22
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author Panigrahi, Trailokyanath
D’Souza, Sharon
Suresh Babu, Vishnu
Dickman, Mor M
Nuijts, Rudy M M A
Sethu, Swaminathan
Shetty, Rohit
author_facet Panigrahi, Trailokyanath
D’Souza, Sharon
Suresh Babu, Vishnu
Dickman, Mor M
Nuijts, Rudy M M A
Sethu, Swaminathan
Shetty, Rohit
author_sort Panigrahi, Trailokyanath
collection PubMed
description PURPOSE: Dry eye disease (DED) is characterized by altered ocular surface proinflammatory and antiinflammatory factors. Interferons (IFNs) are a class of pleiotropic cytokines well known for their antimicrobial, inflammatory, and immunomodulatory roles. Hence, this study investigates the ocular surface expression of different types of IFNs in patients with DED. METHODS: The cross-sectional, observational study included patients with DED and normal subjects. Conjunctival impression cytology (CIC) samples were obtained from the study subjects (controls, n = 7; DED, n = 8). The mRNA expression levels of type 1 IFN (IFNα, IFNβ), type 2 IFN (IFNγ), and type 3 IFN (IFNλ1, IFNλ2, IFNλ3) were measured by quantitative PCR (polymerase chain reaction) in CIC samples. IFNα and IFNγ expression under hyperosmotic stress was also studied in human corneal epithelial cells (HCECs) in vitro. RESULTS: The mRNA expression levels of IFNα and IFNβ were significantly lower and that of IFNγ was significantly higher in DED patients compared to healthy controls. The mRNA levels of IFNα, IFNβ, and IFNλ were significantly lower compared to IFNγ in DED patients. An inverse association between tonicity-responsive enhancer-binding protein (TonEBP; hyperosmotic stress maker) and IFNα or IFNβ expression and a positive association between TonEBP and IFNγ expression was observed in CIC samples. The expression of IFNα was lower than IFNγ in HCECs undergoing hyperosmotic stress compared to HCECs without the stress. CONCLUSION: The presence of an imbalance between type 1 and type 2 IFNs in DED patients suggests newer pathogenic processes in DED, plausible ocular surface infection susceptibility in DED patients, and potential therapeutic targets in the management of DED.
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spelling pubmed-102767292023-06-18 Type 1–type 2 interferon imbalance in dry eye disease Panigrahi, Trailokyanath D’Souza, Sharon Suresh Babu, Vishnu Dickman, Mor M Nuijts, Rudy M M A Sethu, Swaminathan Shetty, Rohit Indian J Ophthalmol Original Article PURPOSE: Dry eye disease (DED) is characterized by altered ocular surface proinflammatory and antiinflammatory factors. Interferons (IFNs) are a class of pleiotropic cytokines well known for their antimicrobial, inflammatory, and immunomodulatory roles. Hence, this study investigates the ocular surface expression of different types of IFNs in patients with DED. METHODS: The cross-sectional, observational study included patients with DED and normal subjects. Conjunctival impression cytology (CIC) samples were obtained from the study subjects (controls, n = 7; DED, n = 8). The mRNA expression levels of type 1 IFN (IFNα, IFNβ), type 2 IFN (IFNγ), and type 3 IFN (IFNλ1, IFNλ2, IFNλ3) were measured by quantitative PCR (polymerase chain reaction) in CIC samples. IFNα and IFNγ expression under hyperosmotic stress was also studied in human corneal epithelial cells (HCECs) in vitro. RESULTS: The mRNA expression levels of IFNα and IFNβ were significantly lower and that of IFNγ was significantly higher in DED patients compared to healthy controls. The mRNA levels of IFNα, IFNβ, and IFNλ were significantly lower compared to IFNγ in DED patients. An inverse association between tonicity-responsive enhancer-binding protein (TonEBP; hyperosmotic stress maker) and IFNα or IFNβ expression and a positive association between TonEBP and IFNγ expression was observed in CIC samples. The expression of IFNα was lower than IFNγ in HCECs undergoing hyperosmotic stress compared to HCECs without the stress. CONCLUSION: The presence of an imbalance between type 1 and type 2 IFNs in DED patients suggests newer pathogenic processes in DED, plausible ocular surface infection susceptibility in DED patients, and potential therapeutic targets in the management of DED. Wolters Kluwer - Medknow 2023-04 2023-04-05 /pmc/articles/PMC10276729/ /pubmed/37026295 http://dx.doi.org/10.4103/IJO.IJO_2842_22 Text en Copyright: © 2023 Indian Journal of Ophthalmology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Panigrahi, Trailokyanath
D’Souza, Sharon
Suresh Babu, Vishnu
Dickman, Mor M
Nuijts, Rudy M M A
Sethu, Swaminathan
Shetty, Rohit
Type 1–type 2 interferon imbalance in dry eye disease
title Type 1–type 2 interferon imbalance in dry eye disease
title_full Type 1–type 2 interferon imbalance in dry eye disease
title_fullStr Type 1–type 2 interferon imbalance in dry eye disease
title_full_unstemmed Type 1–type 2 interferon imbalance in dry eye disease
title_short Type 1–type 2 interferon imbalance in dry eye disease
title_sort type 1–type 2 interferon imbalance in dry eye disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276729/
https://www.ncbi.nlm.nih.gov/pubmed/37026295
http://dx.doi.org/10.4103/IJO.IJO_2842_22
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