Jh. Yamamoto et al., CELLULAR AUTOIMMUNITY TO RETINAL SPECIFIC ANTIGENS IN PATIENTS WITH BEHCETS-DISEASE, British journal of ophthalmology, 77(9), 1993, pp. 584-589
The notion that autoimmune mechanisms play a role in the pathogenesis
of certain uveitic conditions in humans is supported by the observatio
n that lymphocytes from such patients respond in culture against retin
al specific antigens which are uveitogenic in animals. A large proport
ion of uveitis patients with Behcet's disease are reported to respond
well to S antigen, to interphotoreceptor retinoid binding protein (IRB
P) and to several of their uveitogenic peptides, in particular, the S
antigen derived peptide M. Patients with Behcet's disease without ocul
ar involvement were reported not to differ in their responses to S ant
igen from the responses in the control group, yet 35% of them responde
d to IRBP and approximately two thirds of them responded to the peptid
es (peptide M, peptide N, R-4, or R-14). The responses were inhibited
by monoclonal antibodies to CD4 and to class II MHC HLA-DR molecules.
The presence of lymphocyte responses to retinal antigens in patients w
ith Behcet's disease without uveitis might indicate a preclinical stag
e of ocular involvement. Thus, these data support the idea that autoim
munity to retinal specific antigens may play a role in the ocular infl
ammation in Behcet's disease.