Humoral and cellular immune responsiveness to human S-antigen in uveitis

• Published in: Current eye research Vol. 6; no. 7; p. 909
• Main Authors: Doekes, G, van der Gaag, R, Rothova, A, van Kooyk, Y, Broersma, L, Zaal, M J, Dijkman, G, Fortuin, M E, Baarsma, G S, Kijlstra, A
• Format: Journal Article
• Language: English
• Published: England 1987
• Subjects: Adolescent; Adult; Aged; Antibody Formation; Antigens - immunology; Arrestin; Child; Eye Proteins - immunology; Female; Humans; Immunity, Cellular; Male; Middle Aged; Uveitis - immunology
• ISSN: 0271-3683
• DOI: 10.3109/02713688709034859

Purified human retinal S-antigen (S-ag) was used to investigate the occurrence of humoral and cellular autoimmune reactions against S-ag in uveitis patients. With a sensitive ELISA method anti-S-ag antibodies could be detected in the sera of 28% of the uveitis patients. No difference was found between patients with posterior or panuveitis (31 out of 117 positive) and patients with anterior or intermediate uveitis (16 out of 52 positive). Similar frequencies and levels of anti-S-ag autoantibodies were also found among healthy controls (6/20) and patients who had undergone cataract surgery (6/17). Immunoblotting with purified S-ag and with whole human retinal extract confirmed the presence of anti-S-ag antibodies in uveitis and control sera. Moreover, antibodies against various other retinal proteins could also be demonstrated in patients and controls, without being particularly enhanced in uveitis. The cellular immune responsiveness was tested by measuring the production of migration inhibitory factor (MIF) during overnight culture of peripheral mononuclear cells with the antigen. None of 18 healthy controls responded, whereas 17 positive reactions were observed in the group of 44 uveitis patients. The highest frequencies were found in patients with posterior (5/12) or pan- (7/12) uveitis, while of the responders with anterior (2/8) or intermediate (3/12) uveitis, three had disorders affecting the retina. Thus, cellular autoimmune responsiveness to S-ag is apparently associated with posterior and pan-uveitis, and might also occur in non-uveitic retinal disorders, whereas the occurrence of anti-S-ag antibodies is probably not at all pathognomic for uveitis.