In Vivo Confocal Microscopic Evaluation of Corneal Langerhans Cells in Dry Eye Patients§



Federica Machetta 1, Antonio M Fea 1, Alessandro G Actis*, 1, Ugo de Sanctis 1, Paola Dalmasso 2, Federico M Grignolo 1
1 Department of Surgical Sciences, University of Torino, Italy
2 Department of Public Health and Microbiology, Turin University, Italy


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© Machetta et al.; Licensee Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.

* Address correspondence to this author at the Clinica Oculistica Universi-taria, Via Juvarra 19, 1021, Torino, Italy; Tel: +39 011 5666032; Fax: +39 011 539024; E-mail: alessandro.actis@gmail.com
§ This study has been performed with informed consent and following all the guidelines for experimental investigations required in our Department. It was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.


Abstract

Purpose.

To assess inflammatory involvement of cornea in dry eye by means of confocal microscopy, evaluating the presence and distribution of Langherans cells (LCs).

Methods:

98 eyes of 49 subjects were enrolled: 18 subjects affected by Sjögren Syndrome Dry Eye (SSDE), 17 with Non-Sjögren Syndrome Dry Eye (NSSDE), 14 healthy volunteeers. Dry eye symptoms, tear film, ocular surface damage and corneal confocal microscopy were analized.

Results:

A significant increase of LCs density was observed at sub-basal nerve plexus (SSDE = 79 cells/mm2 andNDE = 22 cells/mm2; p = 0,0031) and sub-epithelial nerve plexus (SSDE = 38 cells/mm2 and NDE = 3 cells/mm2; p = 0,0169) in central cornea of SSDE group. An increased number of LCs from the center to the periphery of the cornea was observed, significant only in healthy volunteers group. In dry eye patients there was an increase in LCs density in both peripheral and central cornea with a significant difference between NDE (14,66 cells/mm2) and SSDE (56,66 cells/mm2) only in central cornea (p = 0,0028). In SSDE group, mean density of LCs in central cornea results also superior to NSSDE group (29,33 cells/mm2).

There was no correlation between LCs density and dry eye symptoms, tear film deficiency and ocular surface damage.

Conclusion:

This study demonstrates the activation of an inflammatory and immunological reaction in cornea of NSSDE and SSDE patients. Confocal microscopy can be an important diagnostic tool in evaluation and follow-up of dry eye disease.

Keywords: Confocal microscopy, cornea, dry eye, langherans cells, sj gren.