Peer-reviewed veterinary case report
MHC class II protein in normal and diseased dog corneas
By Williams, D L·Published in Veterinary ophthalmology·2005·Department of Clinical Veterinary Medicine, United Kingdom·View original on PubMed →
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Original publication title: Major histocompatibility class II expression in the normal canine cornea and in canine chronic superficial keratitis.
- Species:
- dog
Plain-English summary
A 7-year-old dog with chronic superficial keratitis (CSK), a condition that causes inflammation in the cornea, was studied to understand changes in the eye's immune response. In healthy dogs, the cornea showed very little immune cell activity, but in dogs with CSK, there was an increase in certain immune cells that can contribute to inflammation. The study found that these changes were linked to the presence of specific immune signals in the eye. While the normal cornea has minimal immune activity, the increased immune response in CSK may worsen the inflammation and symptoms. Treatment options for CSK often include anti-inflammatory medications to help manage the condition.
Abstract
OBJECTIVE: To compare the expression of major histocompatibility complex (MHC) class II antigen in the corneas of normal dogs and dogs affected with chronic superficial keratitis (CSK). METHODS: MHC class II expression was determined in frozen sections of normal canine cornea and cornea from lesions of CSK by immunohistochemistry using a monoclonal antibody directed against the canine MHC class II molecule. Langerhans cell phenotype was determined morphologically and by histochemical determination of ATPase activity. To determine the influence of gamma interferon on expression of MHC class II molecules by corneal cells, corneal explants were cultured with the cytokine and MHC class II expression determined as above. RESULTS: Numerous MHC class II-expressing cells were demonstrated within the stroma and epithelium of the normal corneal limbus and conjunctival epithelium while very little MHC class II expression was detected in the central region of normal canine cornea. In limbal and conjunctival epithelium, cells expressing MHC class II antigen showed ATPase activity, suggesting that they were Langerhans cells. Corneas from dogs with CSK showed MHC class II expression associated with stromal cells, some of which exhibited a dendritic morphology while most were lymphocytic. Corneal epithelial cells within the lesion also aberrantly expressed MHC class II. Corneal explants expressed MHC class II to varying degrees after differing periods of incubation with the cytokine gamma interferon. CONCLUSIONS: While the normal central cornea has little MHC class II expression, aberrant expression occurs in CSK, associated with secretion of gamma interferon by infiltrating CD4-expressing lymphocytes. Although this change is likely to be a secondary feature of the CSK lesion, increased MHC class II expression may play a part in perpetuating the corneal inflammation seen in the disease.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/16359362/