Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012:900:443-69.
doi: 10.1007/978-1-60761-720-4_22.

Rodent models of experimental autoimmune uveitis

Affiliations

Rodent models of experimental autoimmune uveitis

Rajeev K Agarwal et al. Methods Mol Biol. 2012.

Abstract

The model of experimental autoimmune uveitis (EAU) in mice and in rats is described. EAU targets immunologically privileged retinal antigens and serves as a model of autoimmune uveitis in humans as well as a model for autoimmunity in a more general sense. EAU is a well-characterized, robust, and reproducible model that is easily followed and quantitated. It is inducible with synthetic peptides derived from retinal autoantigens in commonly available strains of rats and mice. The ability to induce EAU in various gene-manipulated, including HLA-transgenic, mouse strains makes the EAU model suitable for the study of basic mechanisms as well as in clinically relevant interventions.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Clinical appearance of EAU in the Lewis rat by anterior chamber examination. (a) Normal eye; translucent appearance; pupil and iris blood vessels are clearly visible and the vessels are not congested. (b) Uveitic eye; the eye appears larger due to swelling and proptosis; red reflex is absent and pupil is obscured.
Fig. 2
Fig. 2
Clinical appearance of EAU in the B10.RIII mouse by fundoscopic exam. Eyes were photographed with a fundus camera during the acute phase of disease (day 14–21). The range of disease severity scores parallel the pathological scores in Fig. 3. (Figure adapted from reference 69).
Fig. 3
Fig. 3
Histopathology of EAU in the B10.RIII mouse. Eyes were collected from B10.RIII mice 21 days after uveitogenic immunization with IRBP, representing a range of disease scores. (Figure adapted from references 49, 69). EAU in the rat shows essentially the same type of histopathology.
Fig. 4
Fig. 4
Protocol for induction of autoimmune uveitis in B10.RIII mice with antigen-pulsed DCs (54).

References

    1. Caspi RR. Basic mechanisms in immune-mediated uveitic disease. In: Lightman SL, editor. Immunology of eye disease. Ch. 5. Kluwer Academic Publishers; Lancaster, UK: 1989. pp. 61–86.
    1. Caspi RR, Roberge FG, McAllister CG, el Saied M, Kuwabara T, Gery I, Hanna E, Nussenblatt RB. T cell lines mediating experimental autoimmune uveoretinitis (EAU) in the rat. J Immunol. 1986;136:928–933. - PubMed
    1. Gery I, Robinson WG, Jr, Shichi H, El-Saied M, Mochizuki M, Nussenblatt RB, Williams RM. Differences in susceptibility to experimental autoimmune uveitis among rats of various strains. In: Chandler JW, O’Conner GR, editors. Advances in immunology and immunopathology of the eye; Proceedings of the third international symposium on immunology and immunopathology of the eye; NY: Masson Publishing; 1985. pp. 242–245.
    1. Nussenblatt RB, Whitcup SM, Palestine AG. Uveitis: fundamentals and clinical practice. 2. Mosby - Year Book, Inc.; St. Louis, MO: 1996.
    1. Gery I, Mochizuki M, Nussenblatt RB. Retinal specific antigens and immunopathogenic processes they provoke. Prog Retinal Res. 1986;5:75–109.