May 2003
Volume 44, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2003
Retinal Pigment Epithelium (RPE) Can Either Promote or Inhibit the Activation of Uveitogenic T Cells In Vitro
Author Affiliations & Notes
  • D. Sun
    Ophthalmology, University Louisville, Louisville, KY, United States
  • V. Enzman
    Ophthalmology, University Louisville, Louisville, KY, United States
  • H.J. Kaplan
    Ophthalmology, University Louisville, Louisville, KY, United States
  • H. Shao
    Ophthalmology, University Louisville, Louisville, KY, United States
  • Footnotes
    Commercial Relationships  D. Sun, None; V. Enzman, None; H.J. Kaplan, None; H. Shao, None.
  • Footnotes
    Support  EY12974
Investigative Ophthalmology & Visual Science May 2003, Vol.44, 741. doi:
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      D. Sun, V. Enzman, H.J. Kaplan, H. Shao; Retinal Pigment Epithelium (RPE) Can Either Promote or Inhibit the Activation of Uveitogenic T Cells In Vitro . Invest. Ophthalmol. Vis. Sci. 2003;44(13):741.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: RPE plays an important role in maintaining privileged status of the eye. In this study, we examined the outcomes of in vitro interactions between uveitogenic T cells and non- or activated-RPE. Methods: IRBP-reactive T cell lines and RPE were established. Expression of MHC class II molecules were determined on RPE activated by grade doses of IFN-γ by flow cytometry. Proliferation and cytokine production of IRBP-reactive T cells were measured after pre-exposure to the RPE activated by different doses of IFN-γ. Results: RPE expressed varying levels of MHC class II molecules depending on the concentrations of IFN-γ. IRBP-specific T cells could either be stimulated or inhibited by RPE. The dual effect of RPE is regulated via different levels of MHC class II molecules on RPE. Conclusion: Controlling immune activities of uveitogeneic T cells through varying levels of MHC class II expression on RPE might be one of the regulatory mechanisms by which RPE maintain immune privilege in the eye.

Keywords: retinal pigment epithelium • immunomodulation/immunoregulation • uveitis-clinical/animal model 
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