CD-34 stromal expression pattern in normal and altered human corneas
2002; Elsevier BV; Volume: 109; Issue: 6 Linguagem: Inglês
10.1016/s0161-6420(02)01042-4
ISSN1549-4713
AutoresPaolo Toti, Gian Marco Tosi, Claudio Traversi, Karin Schürfeld, Concetta Cardone, Aldo Caporossi,
Tópico(s)Corneal Surgery and Treatments
ResumoObjective To test CD-34 immunoreactivity in stromal cornea cells in normal and pathologic samples obtained from penetrating keratoplasty. Design Prospective, consecutive histopathologic human tissue study. Participants and controls One hundred two cornea buttons from patients with different diseases, submitted for cornea transplant, were examined. Controls were expired corneas from healthy donor patients who died (n = 4), and globes enucleated for primitive intraocular neoplasias, that is, retinoblastomas (n = 8), and malignant choroidal melanomas (n = 2). Methods The expression of CD-34 in stromal cornea cells was examined by immunohistochemistry analysis. Other immunohistochemical stains included an endothelial cell marker (CD-31), common leukocyte antigen, and α-smooth muscle actin. Main outcome measures Different diseases that may cause blindness and require penetrating keratoplasty have been tested for CD-34 immunoreactivity. Results In control corneas, keratocytes present strong and consistent CD-34 immunoreactivity. Diseases leading to the loss of transparency and penetrating keratoplasty, such as keratoconus, herpes keratitis, trauma, and heredofamilial dystrophies, are associated with focal or diffuse loss of CD-34 expression, whereas pseudophakic bullous keratopathy and Fuchs' endothelial dystrophy show normal CD-34 immunoreactivity in most cases and patchy unstained stromal areas in a few cases. Conclusions Scar tissue formation in the cornea, as in herpes keratitis and trauma, is always associated with loss of CD-34 immunoreactivity, which may otherwise be a primary event in keratoconus and heredofamilial dystrophies. Both in the pseudophakic bullous keratopathy and Fuchs' endothelial dystrophy, CD-34 immunoreactivity may be normal or lost, hence these two diseases may be considered as one and part of the same group with regard to CD-34 expression, as revealed by immunohistochemistry analysis.
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