Immunohistochemical and immunopathologic characterization of superficial stromal immune-mediated keratitis in horses

• Published in: American journal of veterinary research Vol. 73; no. 7; pp. 1067 - 1073
• Main Authors: Pate, Diana O, Clode, Alison B, Olivry, Thierry, Cullen, John M, Salmon, Jacklyn H, Gilger, Brian C
• Format: Journal Article
• Language: English
• Published: United States 01-07-2012
• Subjects: Animals; antibodies; antigens; Aqueous Humor - immunology; B-lymphocytes; blood serum; CD4-positive T-lymphocytes; cornea; cytotoxicity; Female; fluorescent antibody technique; Horse Diseases - immunology; Horse Diseases - pathology; Horses; immunoglobulin A; Immunoglobulin A - analysis; immunoglobulin G; Immunoglobulin G - analysis; immunoglobulin M; Immunoglobulin M - analysis; immunohistochemistry; Immunohistochemistry - veterinary; inflammation; keratitis; Keratitis - immunology; Keratitis - pathology; Keratitis - surgery; Keratitis - veterinary; Male; pathogenesis; Statistics, Nonparametric
• ISSN: 0002-9645; 1943-5681
• DOI: 10.2460/ajvr.73.7.1067

Objective: To describe the immunopathologic characteristics of superficial stromal immune-mediated keratitis (IMMK) immunopathologically by characterizing cellular infiltrate in affected corneas of horses. Animals: 10 client-owned horses with IMMK. Procedures: Immunohistochemical staining was performed on keratectomy samples with equine antibodies against the T-cell marker CD3 and B-cell marker CD79a (10 eyes) and the T-helper cytotoxic marker CD4 and T-cell cytotoxic marker CD8 (6 eyes). Percentage of positively stained cells was scored on a scale from 0 (no cells stained) to 4 (> 75% of cells stained). Equine IgG, IgM, and IgA antibodies were used to detect corneal immunoglobulin via direct immunofluorescence (10 eyes). Serum and aqueous humor (AH) samples from 3 horses with IMMK were used to detect circulating and intraocular IgG against corneal antigens via indirect immunofluorescence on unaffected equine cornea. Results: Percentage scores (scale, 0 to 4) of cells expressing CD3 (median, 2.35 [range, 0.2 to 3.7]; mean ± SD, 2.36 ± 1.08) were significantly greater than scores of cells expressing CD79a (median, 0.55 [range, 0 to 1.5]; mean, 0.69 ± 0.72). All samples stained positively for CD4- and CD8-expressing cells, with no significant difference in scoring. All samples stained positively for IgG, IgM, and IgA. No serum or AH samples collected from horses with IMMK reacted with unaffected equine cornea. Conclusions and Clinical Relevance: Pathogenesis of superficial stromal IMMK included cell-mediated inflammation governed by both cytotoxic and helper T cells. Local immunoglobulins were present in affected corneas; however, corneal-binding immunoglobulins were not detected in the serum or AH from horses with IMMK.