Br J Ophthalmol 1999;83:478-485 ( April )
Modulating phenotype and cytokine production of leucocytic
retinal infiltrate in experimental autoimmune uveoretinitis following
intranasal tolerance induction with retinal antigens
Barbara Laliotou,
Andrew D Dick
Department of
Ophthalmology, University of Aberdeen Medical School, Aberdeen
Correspondence to: Dr Andrew Dick, Department of Ophthalmology, University of Aberdeen
Medical School, Foresterhill, Aberdeen AB25 2ZD.
Accepted for publication 10 November 1998
BACKGROUND/AIM Nasal
administration of retinal antigens induces systemic tolerance which
results in suppression of experimental autoimmune uveoretinitis (EAU)
when subsequently exposed to antigen. The aim was to establish if
tolerance induction alters retinal infiltrating leucocyte phenotype and
cytokine profile in tolerised animals when there is significantly
reduced tissue destruction despite immunisation with retinal antigen.
METHODS Female Lewis
rats were tolerised by intranasal administration with retinal extract
(RE) before immunisation with RE to induce EAU. Control animals were
administered phosphate buffered saline (PBS) intranasally. Post
immunisation, daily clinical responses were recorded and at the height
of disease, retinas were removed and either infiltrating leucocytes
isolated for flow cytometric phenotype assessment and intracellular
cytokine production, or chorioretina processed for
immunohistochemistry. Fellow eyes were assessed for cytokine mRNA by
semiquantitative RT-PCR.
RESULTS Flow
cytometric analysis showed that before clinical onset of EAU there is
no evidence of macrophage infiltration and no significant difference in
circulating T cell populations within the retina. By day 14 a reduced
retinal infiltrate in tolerised animals was observed and in particular
a reduction in numbers of "activated" (with respect to CD4 and MHC
class II expression) macrophages. Immunohistochemistry confirmed these
findings and additionally minimal rod outer segment destruction was
observed histologically. Cytokine analysis revealed that both IL-10
mRNA and intracellular IL-10 production was increased in tolerised eyes
7 days post immunisation. Although by day 14 post immunisation, IL-10
production was equivalent in both groups, a reduced percentage of
IFN- + macrophages and IFN- +
CD4+ T cells with increased percentage of IL-4+
CD4+ T cells were observed in tolerised animals.
CONCLUSIONS Leucocytic
infiltrate is not only reduced in number but its distinct phenotype
compared with controls implies a reduced activation status of
infiltrating monocytes to accompany increased IL-10 and reduced IFN-
production in tolerised animals. This modulation may in turn contribute
towards protection against target organ destruction in EAU.
Keywords:
intranasal tolerance;
experimental autoimmune uveoretinitis;
retina;
cytokines;
flow
cytometry
© 1999 by British Journal of Ophthalmology
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