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  Vol. 103 No. 2, February 1985 TABLE OF CONTENTS
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Identification of Proteins in Contact Lens Surface Deposits by Immunofluorescence Microscopy

Olafur G. Gudmundsson, MD; David F. Woodward, PhD; Sherry A. Fowler, PhD; Mathea R. Allansmith, MD

Arch Ophthalmol. 1985;103(2):196-197.


Abstract

• Worn soft contact lenses from five asymptomatic subjects were examined by immunofluorescence microscopy for type of protein on the lens surface. Lysozyme was the predominant protein component identified by this technique. IgA was also identified in deposits on all five lenses, but the staining was less intense than that for lysozyme. Lactoferrin was identified on the surface of four lenses, one of which stained intensely for this protein and three less intensely. IgG was identified on two contact lenses; the staining was less intense than that for lysozyme. New, never-worn soft contact lenses did not stain for any of the proteins examined in this study. We conclude that several normal tear proteins are capable of contributing to surface deposits on soft contact lenses, and all worn soft contact lenses have protein adherent to their surface as a result of normal wear.



Author Affiliations

From the Department of Ophthalmology, Harvard Medical School (Drs Allansmith and Gudmundsson) and Beth Israel Hospital, Boston (Dr Allansmith); the Department of Cornea Research, Eye Research Institute of Retina Foundation, Boston (Drs Gudmundsson, Fowler, and Allansmith); Allergan Pharmaceuticals, Boston, (Dr Woodward); and Chicago College of Osteopathic Medicine (Dr Fowler). Dr Gudmundsson is a fellow of the World Health Organization.


Footnotes

Accepted for publication April 6, 1984.

Reprint requests to the Landakot Medical Clinic, Marargata 2, 101 Reykjavik, Iceland (Dr Gudmundsson).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Carbohydrate Deposits on the Surfaces of Worn Extended-Wear Soft Contact Lenses
Klotz et al.
Arch Ophthalmol 1987;105:974-977.
ABSTRACT  

Identification of Proteins in Contact Lens Surface Deposits by Immunofluorescence Microscopy
Refojo
Arch Ophthalmol 1985;103:1269-1270.
ABSTRACT  





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