May 2008
Volume 49, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2008
Antimicrobial Peptides: Mediators of Innate Immunity as Templates for the Development of Novel Anti-Infective and Immune Therapeutics
Author Affiliations & Notes
  • V. E. Reviglio
    Cornea & External Diseases, Catholic University of Cordoba, Cordoba, Argentina
    Corneal & External Diseases,
    Cordoba Hospital, Cordoba, Argentina
  • I. C. Kuo
    Cornea Division, Wilmer Eye Institute, Johns Hopkins University,, Baltimore, Maryland
  • R. Sambuelli
    Cornea & External Diseases, Catholic University of Cordoba, Cordoba, Argentina
  • F. Pegoraro
    Cornea & External Diseases,
    Cordoba Hospital, Cordoba, Argentina
  • J. M. Veja
    Cornea & External Diseases,
    Cordoba Hospital, Cordoba, Argentina
  • T. P. O'Brien
    Cornea Department, Bascom Palmer University, Ophthalmology, Miami, Florida
  • Footnotes
    Commercial Relationships  V.E. Reviglio, None; I.C. Kuo, None; R. Sambuelli, None; F. Pegoraro, None; J.M. Veja, None; T.P. O'Brien, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2008, Vol.49, 508. doi:
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      V. E. Reviglio, I. C. Kuo, R. Sambuelli, F. Pegoraro, J. M. Veja, T. P. O'Brien; Antimicrobial Peptides: Mediators of Innate Immunity as Templates for the Development of Novel Anti-Infective and Immune Therapeutics. Invest. Ophthalmol. Vis. Sci. 2008;49(13):508.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Antimicrobial molecules are ancient and essential small cationic molecules of the host defense system found in a wide variety of species. Secretory leukocyte protease inhibitor (SLPI) and Elafin are antimicrobial proteins and members of the innate immunity-associated protein family. The purpose of this study was to investigate the expression of SLPI and Elafin in infected, inflamed human and animal ocular tissues their ability to chemoattract a variety of inflammatory, immune and other cell types; and to determine their functions as antimicrobial and antiprotease agents.

Methods: : Immunohistochemistry, Western blot, ELISA and RT-PCR were used to study the expression and regulation of SLPI and Elafin in a variety of infected and/or inflamed eye samples as follows: 1) Staphylococcus aureus endophthalmitis, 2) S. aureus keratitis, 3) HSV keratitis, 4) Photorefractive keratectomy, 5) keratoconjunctivitis sicca. The transcription levels of SLPI and Elafin mRNA and expression of both proteins from human patients (n=50) and animal eyes samples (n=50) were evaluated.

Results: : Transcription of SLPI and Elafin mRA and expression of both proteins were up-regulated in specific sites of the eye affected by infection and/or inflammation.

Conclusions: : SLPI and Elafin are induced by infection and inflammation, and they are up-regulated in the diseased eye. They may have a key role in development of alternative strategies to prevent ocular infections and regulate the inflammation process.

Keywords: inflammation • immunomodulation/immunoregulation • wound healing 
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