Apoptosis in patients with posterior uveitis
C. C. Chan, D. M. Matteson, Q. Li, S. M. Whitcup and R. B. Nussenblatt
Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, Md 20892-1857, USA. ccc@helix.nih.gov
BACKGROUND: Apoptosis plays a part in the pathogenesis of autoimmune
diseases. OBJECTIVE: To investigate the expression of apoptotic markers in
the eyes of patients with uveitis. METHODS: With the use of
immunohistochemical and in situ apoptotic detection techniques, apoptotic
molecules (Fas or Fas ligand [FasL]) and nuclear DNA fragmentation were
examined in 8 enucleated eyes with Behcet's disease (1), sarcoidosis (1),
subretinal fibrosis and uveitis (1), sympathetic ophthalmia (4), and the
Vogt-Koyanagi-Harada syndrome (1); in 5 chorioretinal biopsy specimens with
acute retinal necrosis (2), multifocal choroiditis (1), sarcoidosis (1),
and subretinal fibrosis and uveitis (1); and in 3 normal control eyes.
RESULTS: Fas and FasL were constitutively expressed in the normal human
retina, but they were expressed much less in the choroid. Increased
expression of Fas and FasL was found in the retina, chorioretinal scar, and
choroidal granulomas in uveitic eyes. However, Fas and FasL expression was
absent in the biopsy specimens with acute retinal necrosis, and little Fas
or FasL was noted on infiltrating lymphocytes. DNA fragmentation was also
identified in eyes with chorioretinal scar and gliosis. CONCLUSIONS:
Apoptosis occurs in uveitic eyes and may play a regulatory role in limiting
ocular inflammation. In uveitic eyes, a dysregulation of the Fas-FasL
apoptotic pathway may lead to gliosis and fibrosis.
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