Literature DB >> 26465889

Contralateral Clinically Unaffected Eyes of Patients With Unilateral Infectious Keratitis Demonstrate a Sympathetic Immune Response.

Andrea Cruzat1, Wolfgang A Schrems2, Laura M Schrems-Hoesl2, Bernardo M Cavalcanti2, Neda Baniasadi2, Deborah Witkin2, Deborah Pavan-Langston2, Reza Dana2, Pedram Hamrah3.   

Abstract

PURPOSE: To analyze the contralateral unaffected eyes of patients with microbial keratitis (MK) for any immune cell or nerve changes by laser in vivo confocal microscopy (IVCM).
METHODS: A prospective study was performed on 28 patients with MK, including acute bacterial, fungal, and Acanthamoeba keratitis, as well as on their contralateral clinically unaffected eyes and on control groups, which consisted of 28 age-matched normal controls and 15 control contact lens (CL) wearers. Laser IVCM with the Heidelberg Retinal Tomograph 3/Rostock Cornea Module and Cochet-Bonnet esthesiometry of the central cornea were performed. Two masked observers assessed central corneal dendritiform cell density and subbasal corneal nerve parameters.
RESULTS: The contralateral clinically unaffected eyes of patients with MK demonstrated significant diminishment in nerve density (15,603.8 ± 1265.2 vs. 24,102.1 ± 735.6 μm/mm²), total number of nerves (11.9 ± 1.0 vs. 24.9 ± 1.2/frame), number of branches (1.7 ± 0.2 vs. 19.9 ± 1.3/frame), and branch nerve length (5775.2 ± 757.1 vs. 12,715.4 ± 648.4 μm/mm²) (P < 0.001 for all parameters) compared to normal controls and CL wearers. Further, dendritiform cell density in the contralateral unaffected eyes was significantly increased as compared to that in controls (117.5 ± 19.9 vs. 24.2 ± 3.5 cells/mm², P < 0.001).
CONCLUSIONS: We demonstrate a subclinical involvement in the contralateral clinically unaffected eyes in patients with unilateral acute MK. In vivo confocal microscopy reveals not only a diminishment of the subbasal corneal nerves and sensation, but also an increase in dendritiform cell density in the contralateral unaffected eyes of MK patients. These findings show bilateral immune alterations in a clinically unilateral disease.

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Mesh:

Year:  2015        PMID: 26465889      PMCID: PMC4611956          DOI: 10.1167/iovs.15-16560

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  43 in total

Review 1.  In vivo confocal microscopy of corneal nerves: analysis and clinical correlation.

Authors:  Andrea Cruzat; Deborah Pavan-Langston; Pedram Hamrah
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Review 2.  Corneal immunity is mediated by heterogeneous population of antigen-presenting cells.

Authors:  Pedram Hamrah; Syed O Huq; Ying Liu; Qiang Zhang; M Reza Dana
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Review 3.  Corneal nerves: structure, contents and function.

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Journal:  Exp Eye Res       Date:  2003-05       Impact factor: 3.467

4.  In vivo confocal microscopic evaluation of langerhans cell density and distribution in the corneal epithelium of healthy volunteers and contact lens wearers.

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6.  Corneal toxicity of propamidine.

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7.  Neurogenic influences on contralateral responses during experimental rat monoarthritis.

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8.  Unilateral herpes zoster ophthalmicus results in bilateral corneal nerve alteration: an in vivo confocal microscopy study.

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  20 in total

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3.  Impact of herpetic stromal immune keratitis in corneal biomechanics and innervation.

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4.  In vivo confocal microscopy detects bilateral changes of corneal immune cells and nerves in unilateral herpes zoster ophthalmicus.

Authors:  Bernardo M Cavalcanti; Andrea Cruzat; Afsun Sahin; Deborah Pavan-Langston; Eric Samayoa; Pedram Hamrah
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Review 5.  In Vivo Confocal Microscopy of Corneal Nerves in Health and Disease.

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6.  Defining an Optimal Sample Size for Corneal Epithelial Immune Cell Analysis Using in vivo Confocal Microscopy Images.

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7.  Widespread effects of clinically unilateral focal nerve injuries.

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Review 8.  Corneal pain and experimental model development.

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Review 9.  Bilateral Alterations in Corneal Nerves, Dendritic Cells, and Tear Cytokine Levels in Ocular Surface Disease.

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Review 10.  A Review of Imaging Biomarkers of the Ocular Surface.

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