TY - GEN
T1 - In-vivo immunofluorescence confocal microscopy of herpes simplex virus type 1 keratitis
AU - Kaufman, Stephen C.M.D.
AU - Laird, Jeffery A.
AU - Beuerman, Roger W.
PY - 1996/1/1
Y1 - 1996/1/1
N2 - The white-light confocal microscope offers an in vivo, cellular-level resolution view of the cornea. This instrument has proven to be a valuable research and diagnostic tool for the study of infectious keratitis. In this study, we investigate the direct visualization of herpes simplex virus type 1 (HSV-1)-infected corneal epithelium, with in vivo confocal microscopy, using HSV-1 immunofluorescent antibodies. New Zealand white rabbits were infected with McKrae strain of HSV-1 in one eye; the other eye of each rabbit was used as an uninfected control. Four days later, the rabbits were anesthetized and a cellulose sponge was applied to each cornea, and a drop of direct HSV fluorescein-tagged antibody was placed on each sponge every 3 to 5 minutes for 1 hour. Fluorescence confocal microscopy was then performed. The HSV-infected corneas showed broad regions of hyperfluorescent epithelial cells. The uninfected corneas revealed no background fluorescence. Thus, using the confocal microscope with a fluorescent cube, we were able to visualize HSV-infected corneal epithelial cells tagged with a direct fluorescent antibody. This process may prove to be a useful clinical tool for the in vivo diagnosis of HSV keratitis.
AB - The white-light confocal microscope offers an in vivo, cellular-level resolution view of the cornea. This instrument has proven to be a valuable research and diagnostic tool for the study of infectious keratitis. In this study, we investigate the direct visualization of herpes simplex virus type 1 (HSV-1)-infected corneal epithelium, with in vivo confocal microscopy, using HSV-1 immunofluorescent antibodies. New Zealand white rabbits were infected with McKrae strain of HSV-1 in one eye; the other eye of each rabbit was used as an uninfected control. Four days later, the rabbits were anesthetized and a cellulose sponge was applied to each cornea, and a drop of direct HSV fluorescein-tagged antibody was placed on each sponge every 3 to 5 minutes for 1 hour. Fluorescence confocal microscopy was then performed. The HSV-infected corneas showed broad regions of hyperfluorescent epithelial cells. The uninfected corneas revealed no background fluorescence. Thus, using the confocal microscope with a fluorescent cube, we were able to visualize HSV-infected corneal epithelial cells tagged with a direct fluorescent antibody. This process may prove to be a useful clinical tool for the in vivo diagnosis of HSV keratitis.
UR - http://www.scopus.com/inward/record.url?scp=0029727196&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0029727196&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:0029727196
SN - 0819420476
SN - 9780819420473
T3 - Proceedings of SPIE - The International Society for Optical Engineering
SP - 2
EP - 5
BT - Proceedings of SPIE - The International Society for Optical Engineering
A2 - Parel, Jean-Marie
A2 - Joos, Karen M.
A2 - Rol, Pascal O.
T2 - Ophthalmic Technologies VI
Y2 - 27 January 1996 through 28 January 1996
ER -