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Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1989 Sep;77(3):422–427.

Morphometric analysis of T lymphocyte compartmentation in experimental autoimmune uveoretinitis.

E C Brown 1, E Kasp 1, D C Dumonde 1
PMCID: PMC1542065  PMID: 2805411

Abstract

Experimental autoimmune uveoretinitis (EAU) in the Lewis rat is characterized by extensive infiltration of inflammatory cells into all compartments of the eye, only some of which become irreversibly damaged. The apparent differences in the pathogenic impact of inflammatory cells within different ocular compartments may suggest that different mechanisms underlie cellular infiltration and selective tissue destruction. In order to investigate the importance of T lymphocyte infiltration, we carried out a precise topographical and temporal analysis of T cell infiltration into five compartments of the eye using an improved method for the fixation of ocular tissue. Our study showed that T cell infiltration began in the ciliary body and was most numerous and sustained in this area during EAU. The peak of T cell infiltration into the retina was comparatively delayed and was of lesser magnitude. Analysis of T cell subsets revealed a tendency for the helper phenotype to predominant during the course of disease in all ocular compartments except the retina where both helper and cytotoxic/suppressor T cells were equally represented at the height of inflammation. We suggest that the pathogenetic impact of autoreactive lymphocytes in EAU depends on the accessibility of relevant tissue antigen and on local microenvironmental features of lymphocytic traffic within different ocular compartments.

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Selected References

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  1. Caspi R. R., Roberge F. G., McAllister C. G., el-Saied M., Kuwabara T., Gery I., Hanna E., Nussenblatt R. B. T cell lines mediating experimental autoimmune uveoretinitis (EAU) in the rat. J Immunol. 1986 Feb 1;136(3):928–933. [PubMed] [Google Scholar]
  2. Chan C. C., Mochizuki M., Nussenblatt R. B., Palestine A. G., McAllister C., Gery I., BenEzra D. T-lymphocyte subsets in experimental autoimmune uveitis. Clin Immunol Immunopathol. 1985 Apr;35(1):103–110. doi: 10.1016/0090-1229(85)90083-2. [DOI] [PubMed] [Google Scholar]
  3. Chan C. C., Mochizuki M., Palestine A. G., BenEzra D., Gery I., Nussenblatt R. B. Kinetics of T-lymphocyte subsets in the eyes of Lewis rats with experimental autoimmune uveitis. Cell Immunol. 1985 Dec;96(2):430–434. doi: 10.1016/0008-8749(85)90373-9. [DOI] [PubMed] [Google Scholar]
  4. Dumonde D. C., Kasp-Grochowska E., Graham E., Sanders M. D., Faure J. P., de Kozak Y., van Tuyen V. Anti-retinal autoimmunity and circulating immune complexes in patients with retinal vasculitis. Lancet. 1982 Oct 9;2(8302):787–792. doi: 10.1016/s0140-6736(82)92679-4. [DOI] [PubMed] [Google Scholar]
  5. Guesdon J. L., Ternynck T., Avrameas S. The use of avidin-biotin interaction in immunoenzymatic techniques. J Histochem Cytochem. 1979 Aug;27(8):1131–1139. doi: 10.1177/27.8.90074. [DOI] [PubMed] [Google Scholar]
  6. Kasp E., Banga J. P., Brown E. C., Wicking J. M., Suleyman S., Ellis B. A., Sanders M. D., Dumonde D. C. An improved method for the purification of retinal S-antigen using selective hydrophobic adsorption chromatography. J Immunol Methods. 1987 Jun 26;100(1-2):147–152. doi: 10.1016/0022-1759(87)90183-9. [DOI] [PubMed] [Google Scholar]
  7. McLean I. W., Nakane P. K. Periodate-lysine-paraformaldehyde fixative. A new fixation for immunoelectron microscopy. J Histochem Cytochem. 1974 Dec;22(12):1077–1083. doi: 10.1177/22.12.1077. [DOI] [PubMed] [Google Scholar]
  8. Nussenblatt R. B., Gery I., Wacker W. B. Experimental autoimmune uveitis: cellular immune responsiveness. Invest Ophthalmol Vis Sci. 1980 Jun;19(6):686–690. [PubMed] [Google Scholar]
  9. Rozenszajn L. A., Muellenberg-Coulombre C., Gery I., el-Saied M., Kuwabara T., Mochizuki M., Lando Z., Nussenblatt R. B. Induction of experimental autoimmune uveoretinitis by T-cell lines. Immunology. 1986 Apr;57(4):559–565. [PMC free article] [PubMed] [Google Scholar]
  10. Salinas-Carmona M. C., Nussenblatt R. B., Gery I. Experimental autoimmune uveitis in the athymic nude rat. Eur J Immunol. 1982 Jun;12(6):480–484. doi: 10.1002/eji.1830120606. [DOI] [PubMed] [Google Scholar]
  11. Wacker W. B., Donoso L. A., Kalsow C. M., Yankeelov J. A., Jr, Organisciak D. T. Experimental allergic uveitis. Isolation, characterization, and localization of a soluble uveitopathogenic antigen from bovine retina. J Immunol. 1977 Dec;119(6):1949–1958. [PubMed] [Google Scholar]
  12. Zaal J., Doekes G., Breebaart A. C., Kijlstra A. Quantitative determination of S-antigen in human ocular tissues, aqueous humour and serum. Curr Eye Res. 1986 Oct;5(10):763–775. doi: 10.3109/02713688609000018. [DOI] [PubMed] [Google Scholar]
  13. de Kozak Y., Sakai J., Thillaye B., Faure J. P. S antigen-induced experimental autoimmune uveo-retinitis in rats. Curr Eye Res. 1981;1(6):327–337. doi: 10.3109/02713688108998359. [DOI] [PubMed] [Google Scholar]

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