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Blood-retina barrier dysfunction in experimental autoimmune uveitis: the pathogenesis and therapeutic targets

  • Jeongtae Kim (Department of Anatomy, Kosin University College of Medicine) ;
  • Jiyoon Chun (Department of Veterinary Anatomy, College of Veterinary Medicine and Veterinary Medical Research Institute, Jeju National University) ;
  • Meejung Ahn (Department of Animal Science, College of Life Science, Sangji University) ;
  • Kyungsook Jung (Functional Biomaterials Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Changjong Moon (Department of Veterinary Anatomy, College of Veterinary Medicine and BK21 Plus Project Team, Chonnam National University) ;
  • Taekyun Shin (Department of Veterinary Anatomy, College of Veterinary Medicine and Veterinary Medical Research Institute, Jeju National University)
  • Received : 2021.11.12
  • Accepted : 2022.01.06
  • Published : 2022.03.31

Abstract

Experimental autoimmune uveitis (EAU), an animal model of human uveitis, is characterized by infiltration of autoimmune T cells in the uvea as well as in the retina of susceptible animals. EAU is induced by the immunization of uveitogenic antigens, including either retinal soluble-antigen or interphotoreceptor retinoid-binding proteins, in Lewis rats. The pathogenesis of EAU in rats involves the proliferation of autoimmune T cells in peripheral lymphoid tissues and breakdown of the blood-retinal barrier, primarily in the uvea and retina, finally inducing visual dysfunction. In this review, we describe recent EAU studies to facilitate the design of a therapeutic strategy through the interruption of uveitogenic factors during the course of EAU, which will be helpful for controlling human uveitis.

Keywords

Acknowledgement

This research was supported by the National Research Foundation of Korea (Grant number: NRF- 2019R1A2C1087753) and a grant from Kosin University College of Medicine (2021).

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