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Updated: Aug 12, 2026

Ex Vivo Organotypic Corneal Model of Acute Epithelial Herpes Simplex Virus Type I Infection
Published on: November 3, 2012
Intercellular adhesion molecule-1 (ICAM-1) and HLA-DR antigens in herpes keratitis
V M Elner1, S Dutt, M A Pavilack
1W.K. Kellogg Eye Center, University of Michigan, Ann Arbor 48105.
Insights
Intercellular adhesion molecule-1 (ICAM-1) is present in human corneal disease, specifically herpes simplex virus (HSV) keratitis. This finding suggests ICAM-1 and HLA-DR co-expression are key in immune responses and leukocyte interactions within the cornea.
Area of Science:
- Ophthalmology
- Immunology
- Cell Biology
Background:
- Intercellular adhesion molecule-1 (ICAM-1) is a cell surface glycoprotein involved in leukocyte adhesion and trafficking during inflammation.
- ICAM-1 has been observed in cytokine-exposed human corneas but not previously reported in corneal disease.
- Herpes simplex virus (HSV) keratitis is a significant cause of corneal disease and inflammation.
Purpose of the Study:
- To investigate the presence and role of ICAM-1 in human disciform herpes simplex virus (HSV) keratitis.
- To determine if ICAM-1 expression is altered in corneal tissue affected by HSV keratitis.
Main Methods:
- Immunohistochemistry was utilized to detect ICAM-1 expression in five human corneal specimens.
- Specimens included keratoplasty samples from patients with disciform HSV keratitis and a biopsy from a patient with HSV keratoscleritis.
- Monoclonal antibodies specific to ICAM-1 were used, with negative controls including antibodies to other adhesion molecules and mouse serum.
Main Results:
- Intense ICAM-1 immunoreactivity was observed in keratinocytes, stromal keratocytes, and endothelial cells across all five specimens.
- ICAM-1 expression was predominantly localized to areas of leukocytic infiltration.
- Diffuse, intense HLA-DR positivity was detected throughout the corneas, and control antibodies showed no reactivity.
Conclusions:
- This study provides the first evidence of ICAM-1 expression in human corneal disease, specifically HSV keratitis.
- The co-expression of ICAM-1 and HLA-DR suggests a significant role in the immune response within the cornea during HSV keratitis.
- Elevated ICAM-1 in leukocyte-infiltrated regions may mediate leukocyte-corneal cell binding, contributing to immune-mediated damage.
Purpose:
Intercellular adhesion molecule-1 (ICAM-1) is a cell surface glycoprotein that binds leukocyte function antigen-1 receptor on leukocytes, thereby regulating leukocyte trafficking and function at sites of inflammation. Recently, the authors demonstrated ICAM-1 in human corneas exposed to proinflammatory cytokines, but ICAM-1 has not been reported in corneal disease. In this study, the presence of ICAM-1 in human disciform herpes simplex virus (HSV) keratitis is investigated.
Methods:
Immunohistochemistry was performed for ICAM-1 on 4 keratoplasty specimens from patients with corneal scarring due to disciform HSV keratitis and 1 corneoscleral biopsy of a patient with active HSV keratoscleritis using specific, characterized monoclonal antibody to ICAM-1. Negative immunohistochemical controls included monoclonal antibodies to other vascular endothelial adhesion molecules or mouse serum.
Results:
All 5 specimens demonstrated intense ICAM-1 immunoreactivity of keratinocytes, stromal keratocytes, and endothelial cells, predominantly in regions of leukocytic infiltration. Diffuse, intense HLA-DR positivity was detected throughout the corneas. The specimens failed to react with control antibodies.
Conclusion:
These results are the first to demonstrate ICAM-1 in human corneal disease and suggest important roles for ICAM-1 and HLA-DR co-expression in generating immune responses in HSV keratitis. Increased ICAM-1 expression in regions of leukocytic infiltration may regulate leukocyte-corneal cell binding, thereby promoting immune responses and damage by activated leukocytes.
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