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Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper
PURPOSE: Conventionally, keratoconus (KC) has been considered a noninflammatory corneal ectatic disorder. Recent evidence suggests a possible role of inflammation in the pathogenesis of KC. Hence, we analyzed the levels of inflammatory factors in the tear fluid of Indian KC patients. METHODS: Tear f...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700575/ https://www.ncbi.nlm.nih.gov/pubmed/29133633 http://dx.doi.org/10.4103/ijo.IJO_233_17 |
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author | Shetty, Rohit Deshmukh, Rashmi Ghosh, Arkasubhra Sethu, Swaminathan Jayadev, Chaitra |
author_facet | Shetty, Rohit Deshmukh, Rashmi Ghosh, Arkasubhra Sethu, Swaminathan Jayadev, Chaitra |
author_sort | Shetty, Rohit |
collection | PubMed |
description | PURPOSE: Conventionally, keratoconus (KC) has been considered a noninflammatory corneal ectatic disorder. Recent evidence suggests a possible role of inflammation in the pathogenesis of KC. Hence, we analyzed the levels of inflammatory factors in the tear fluid of Indian KC patients. METHODS: Tear fluid samples were collected from age- and sex-matched healthy controls and KC patients (with different grades). The levels of the inflammatory factors in tears were analyzed using cytometric bead array (Human Soluble Protein Flex Set System, BD Biosciences) for levels of interleukin-1α (IL-1α), IL-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-9, IL-10, IL-12p70, IL-23p40, IL-13, IL-17A, IL-17F, IL-21, interferon-α (IFNα), IFNγ, tumor necrosis factor-α, CCL2/monocyte chemotactic protein-1, CCL4/macrophage inflammatory protein-1β (MIP-1β), MIP-1α, CCL5/RANTES, CXCL10/IP10, ICAM1, CD62E, vascular endothelial growth factor and transforming growth factor β. RESULTS: An increase in Kmax and Kmean, and a decrease in central corneal thickness was observed with increasing grades of KC. Tear analysis showed that most of the tear soluble factors, including cytokines, chemokines, growth factors and cell adhesion molecules were significantly elevated in the KC patients compared to the controls. CONCLUSION: Our findings suggest that inflammatory factors associated with KC may play a role in its pathogenesis. This opens the potential to explore anti-inflammatory strategies to either halt or delay the progression of KC. |
format | Online Article Text |
id | pubmed-5700575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57005752017-12-01 Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper Shetty, Rohit Deshmukh, Rashmi Ghosh, Arkasubhra Sethu, Swaminathan Jayadev, Chaitra Indian J Ophthalmol Featured Original Article PURPOSE: Conventionally, keratoconus (KC) has been considered a noninflammatory corneal ectatic disorder. Recent evidence suggests a possible role of inflammation in the pathogenesis of KC. Hence, we analyzed the levels of inflammatory factors in the tear fluid of Indian KC patients. METHODS: Tear fluid samples were collected from age- and sex-matched healthy controls and KC patients (with different grades). The levels of the inflammatory factors in tears were analyzed using cytometric bead array (Human Soluble Protein Flex Set System, BD Biosciences) for levels of interleukin-1α (IL-1α), IL-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-9, IL-10, IL-12p70, IL-23p40, IL-13, IL-17A, IL-17F, IL-21, interferon-α (IFNα), IFNγ, tumor necrosis factor-α, CCL2/monocyte chemotactic protein-1, CCL4/macrophage inflammatory protein-1β (MIP-1β), MIP-1α, CCL5/RANTES, CXCL10/IP10, ICAM1, CD62E, vascular endothelial growth factor and transforming growth factor β. RESULTS: An increase in Kmax and Kmean, and a decrease in central corneal thickness was observed with increasing grades of KC. Tear analysis showed that most of the tear soluble factors, including cytokines, chemokines, growth factors and cell adhesion molecules were significantly elevated in the KC patients compared to the controls. CONCLUSION: Our findings suggest that inflammatory factors associated with KC may play a role in its pathogenesis. This opens the potential to explore anti-inflammatory strategies to either halt or delay the progression of KC. Medknow Publications & Media Pvt Ltd 2017-11 /pmc/articles/PMC5700575/ /pubmed/29133633 http://dx.doi.org/10.4103/ijo.IJO_233_17 Text en Copyright: © 2017 Indian Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Featured Original Article Shetty, Rohit Deshmukh, Rashmi Ghosh, Arkasubhra Sethu, Swaminathan Jayadev, Chaitra Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper |
title | Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper |
title_full | Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper |
title_fullStr | Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper |
title_full_unstemmed | Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper |
title_short | Altered tear inflammatory profile in Indian keratoconus patients - The 2015 Col Rangachari Award paper |
title_sort | altered tear inflammatory profile in indian keratoconus patients - the 2015 col rangachari award paper |
topic | Featured Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700575/ https://www.ncbi.nlm.nih.gov/pubmed/29133633 http://dx.doi.org/10.4103/ijo.IJO_233_17 |
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