March 1993
Volume 34, Issue 3
Free
Articles  |   March 1993
Monoclonal antibody against CD11b/CD18 inhibits endotoxin-induced uveitis.
Author Affiliations
  • S M Whitcup
    Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.
  • L R DeBarge
    Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.
  • H Rosen
    Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.
  • R B Nussenblatt
    Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.
  • C C Chan
    Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.
Investigative Ophthalmology & Visual Science March 1993, Vol.34, 673-681. doi:
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      S M Whitcup, L R DeBarge, H Rosen, R B Nussenblatt, C C Chan; Monoclonal antibody against CD11b/CD18 inhibits endotoxin-induced uveitis.. Invest. Ophthalmol. Vis. Sci. 1993;34(3):673-681.

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Abstract

PURPOSE: To examine the serial expression of cell adhesion molecules in C3H/HeN mice with endotoxin-induced uveitis, and to study the effect of treatment with a monoclonal antibody against Mac-1 on the development of endotoxin-induced uveitis. METHODS: Immunohistochemical staining was used to document the serial expression of Mac-1, intercellular adhesion molecule-1 (ICAM-1), and lymphocyte function-associated antigen-1 (LFA-1) in eyes of C3H/HeN mice with endotoxin-induced uveitis. Then, in two separate experiments, endotoxin-induced uveitis was produced in a total of 48 mice by injecting Salmonella typhimurium endotoxin into one hind footpad. At the time of endotoxin injection, 24 mice received an intraperitoneal injection of anti-Mac-1 antibody and 24 control mice received an intraperitoneal injection of rat IgG. Histopathologic sections of eyes taken 24 hours after endotoxin injection were graded by two masked observers on a scale of 0 to 4. RESULTS: Intercellular adhesion molecule-1 was first expressed on the ciliary body epithelium 6 hr after endotoxin injection and Mac-1 and LFA-1 were expressed on infiltrating inflammatory cells 12 hr after endotoxin injection. Treatment with anti-MAC-1 antibody significantly inhibited the development of ocular inflammation when compared with treatment with control IgG (P < 0.001). CONCLUSION: Intercellular adhesion molecule-1 is expressed in the eye before clinical or histologic signs of inflammation. Furthermore, treatment with antibody against Mac-1 significantly inhibits the development of endotoxin-induced uveitis in mice and suggests that anti-Mac-1 antibody may be useful for treating acute ocular inflammation.

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