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Lymphocyte subsets in conjunctival mucosa-associated-lymphoid-tissue after exposure to retinal-S-antigen

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Abstract

Purpose : To evaluate the immune cell subsets in conjunctival mucosa-associated-lymphoid-tissue (C-MALT) following challenge with antigen.

Methods : Ten adult female Lewis rats were studied. Five rats received one drop (5 μL) of retinal S-antigen (500 μg/mL in phosphate buffered saline, PBS) instilled into the lower fornix twice daily for 10 consecutive days. Five rats received PBS only and served as controls for the experiment. Two days after the last instillation the animals were sacrificed and the orbital contents prepared for immunohistological staining. A panel of monoclonal antibodies was used: CD5, CD4, CD8, CD25, and CD45RA. The number of positive cells were counted in sections of epibulbar, forniceal, and tarsal conjunctiva.

Results : There was a significant increase in the number of CD8+ T lymphocytes in the conjunctiva of animals receiving retinal S-antigen when compared to control animals.

Conclusion : Conjunctival instillation of retinal S-antigen causes an immune response in the C-MALT with a significant increase in the CD8+ T lymphocyte subset in this tissue. This response may be involved in the induction of tolerance to the encountered antigen.

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References

  1. Higgins PJ, Weiner HL. Suppression of experimental auto immune encephalomyelitis by oral administration of myelin basic protein and its fragments. J Immunol 1988; 140: 440¶ 445.

    PubMed  CAS  Google Scholar 

  2. Lider O, Santos LMB, Lee CSY et al. Suppression of experimental autoimmune encephalomyelitis by oral administration of myelin basic protein. J Immunol 1989; 142: 748¶ 752.

    PubMed  CAS  Google Scholar 

  3. Nussenblatt RB, Caspi RR, Mahid R et al. Inhibition of S-antigen induced experimental autoimmune uveoretinitis by oral induction of tolerance with S-antigen. J Immunol 1990; 144: 1689¶ 1695.

    PubMed  CAS  Google Scholar 

  4. Vrabec TR, Gregerson DS, Dua HS, Donoso LA. Inhibition of experimental autoimmune uveoretinitis by oral administration of S-antigen and synthetic peptides. Autoimmunity 1992; 12: 175¶ 184.

    PubMed  CAS  Google Scholar 

  5. He Y, Mellon J, Niederkorn JY. The effect of oral immunization on corneal allograft survival. Transplantation 1996; 61: 920¶ 926.

    Article  PubMed  CAS  Google Scholar 

  6. Zhang Z, Lee C, Weiner H. Suppression of adjuvant arthritis by oral administration of type II collagen. J Immunol 1980; 145: 2489.

    Google Scholar 

  7. Zhang Z, Davidson L, Elisenbarth G, Weiner H. Suppression of diabetes in nonobese diabetic mice by oral administration of porcine insulin. Proc Natl Acad Sci USA 1991; 88: 10252.

    Article  PubMed  CAS  Google Scholar 

  8. Dick AD, Cheng YE, McKinnon A et al. Nasal administration of retinal antigens suppresses the inflammatory response in experimental allergic uveoretinitis. Br J Ophthalmol 1993; 77: 171¶ 175.

    PubMed  CAS  Google Scholar 

  9. Dua HS, Donoso LA, Laibson PR. Conjunctival instillation of retinal antigens induces tolerance. Does it invoke mucosal tolerance mediated via conjunctival associated lymphoid tissue (CALT)? Ocular Immunol Inflam 1994; 2: 29¶ 36

    Google Scholar 

  10. Egan RM, Stevens J, Yorkey CM et al. Murine conjunctival tolerance and the fate of antigen specific T cells. Invest Ophthalmol Vis Sci 1996 (suppl); 37: 1067.

    Google Scholar 

  11. Dua HS, Gomes JAP, Jindal VK et al. Mucosa specific lymphocytes in the human conjunctiva, corneoscleral limbus and lacrimal gland. Curr Eye Res 1994; 13: 87¶ 93.

    PubMed  CAS  Google Scholar 

  12. Dua HS, Gomes JAP, Donoso LA, Laibson PR. The ocular surface as part of the mucosal immune system: conjunctival mucosal-specific lymphocytes in ocular surface pathology. Eye 1995; 9: 361¶ 367.

    Google Scholar 

  13. Dua HS, Jindal VK, Gomes JAP, Amoaku WA, Donoso LA, Laibson PR, Mahlberg K. The effect of topical cyclosporin on conjunctiva-associated lymphoid tissue (CALT). Eye 1996; 10: 433¶ 438.

    PubMed  Google Scholar 

  14. Allansmith MR, Gudmundsson OG, Harm LB et al. The immune response of the lacrimal gland to antigenic exposure. Curr Eye Res 1987; 6: 289¶ 294.

    Google Scholar 

  15. Ebersole JL, Stefen MJ, Pappo J. Secretory immune responses in ageing rat. II. Phenotype distribution of leukocytes in secretory and lymphoid tissues. Immunology 1988; 64: 289¶ 294.

    PubMed  CAS  Google Scholar 

  16. Montgomery PC, Peppard JV, Skandera CA. A comparison of lymphocyte subset distribution in rat lacrimal glands with cells from tissues of mucosal and non-mucosal origin. Curr Eye Res 1990; 9: 85¶ 93.

    PubMed  CAS  Google Scholar 

  17. Gomes JAP, Jindal VK, Gormley PD, Dua HS. Phenotypic analysis of resident lymphoid cells in the conjunctiva and adnexal tissues of rat. Exp Eye Res 1997; 64: 991¶ 997

    Article  PubMed  CAS  Google Scholar 

  18. Holt PG, Leivers S. Tolerance induction via antigen inhalation: idiotype specificity, stability and involvement of suppressor T-cells. Int Arch Allergy Appl Immunol 1982; 67: 155¶ 160.

    PubMed  CAS  Google Scholar 

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Gormley, P.D., Powell-Richards, A.O.R., Azuara-Blanco, A. et al. Lymphocyte subsets in conjunctival mucosa-associated-lymphoid-tissue after exposure to retinal-S-antigen. Int Ophthalmol 22, 77–80 (1998). https://doi.org/10.1023/A:1006191022900

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  • DOI: https://doi.org/10.1023/A:1006191022900

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