BJO

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this link to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Laliotou, B.
Right arrow Articles by Dick, A. D
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Laliotou, B.
Right arrow Articles by Dick, A. D
Br J Ophthalmol 1999;83:478-485 ( April )

Modulating phenotype and cytokine production of leucocytic retinal infiltrate in experimental autoimmune uveoretinitis following intranasal tolerance induction with retinal antigens

Barbara Laliotou, Andrew D Dick

Department of Ophthalmology, University of Aberdeen Medical School, Aberdeen

Correspondence to: Dr Andrew Dick, Department of Ophthalmology, University of Aberdeen Medical School, Foresterhill, Aberdeen AB25 2ZD.

Accepted for publication 10 November 1998

BACKGROUND/AIM---Nasal administration of retinal antigens induces systemic tolerance which results in suppression of experimental autoimmune uveoretinitis (EAU) when subsequently exposed to antigen. The aim was to establish if tolerance induction alters retinal infiltrating leucocyte phenotype and cytokine profile in tolerised animals when there is significantly reduced tissue destruction despite immunisation with retinal antigen.
METHODS---Female Lewis rats were tolerised by intranasal administration with retinal extract (RE) before immunisation with RE to induce EAU. Control animals were administered phosphate buffered saline (PBS) intranasally. Post immunisation, daily clinical responses were recorded and at the height of disease, retinas were removed and either infiltrating leucocytes isolated for flow cytometric phenotype assessment and intracellular cytokine production, or chorioretina processed for immunohistochemistry. Fellow eyes were assessed for cytokine mRNA by semiquantitative RT-PCR.
RESULTS---Flow cytometric analysis showed that before clinical onset of EAU there is no evidence of macrophage infiltration and no significant difference in circulating T cell populations within the retina. By day 14 a reduced retinal infiltrate in tolerised animals was observed and in particular a reduction in numbers of "activated" (with respect to CD4 and MHC class II expression) macrophages. Immunohistochemistry confirmed these findings and additionally minimal rod outer segment destruction was observed histologically. Cytokine analysis revealed that both IL-10 mRNA and intracellular IL-10 production was increased in tolerised eyes 7 days post immunisation. Although by day 14 post immunisation, IL-10 production was equivalent in both groups, a reduced percentage of IFN-gamma + macrophages and IFN-gamma + CD4+ T cells with increased percentage of IL-4+ CD4+ T cells were observed in tolerised animals.
CONCLUSIONS---Leucocytic infiltrate is not only reduced in number but its distinct phenotype compared with controls implies a reduced activation status of infiltrating monocytes to accompany increased IL-10 and reduced IFN-gamma production in tolerised animals. This modulation may in turn contribute towards protection against target organ destruction in EAU.

Keywords: intranasal tolerance; experimental autoimmune uveoretinitis; retina; cytokines; flow cytometry


© 1999 by British Journal of Ophthalmology



This article has been cited by other articles:


Home page
Int ImmunolHome page
S. R. Thurau, T. R. Mempel, A. Flugel, M. Diedrichs-Mohring, F. Krombach, N. Kawakami, and G. Wildner
The fate of autoreactive, GFP+ T cells in rat models of uveitis analyzed by intravital fluorescence microscopy and FACS
Int. Immunol., November 1, 2004; 16(11): 1573 - 1582.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
K.-H. Sonoda, Y. Sasa, H. Qiao, C. Tsutsumi, T. Hisatomi, S. Komiyama, T. Kubota, T. Sakamoto, Y.-I. Kawano, and T. Ishibashi
Immunoregulatory Role of Ocular Macrophages: The Macrophages Produce RANTES to Suppress Experimental Autoimmune Uveitis
J. Immunol., September 1, 2003; 171(5): 2652 - 2659.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
C. Broderick, R. M. Hoek, J. V. Forrester, J. Liversidge, J. D. Sedgwick, and A. D. Dick
Constitutive Retinal CD200 Expression Regulates Resident Microglia and Activation State of Inflammatory Cells during Experimental Autoimmune Uveoretinitis
Am. J. Pathol., November 1, 2002; 161(5): 1669 - 1677.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Ophthalmol.Home page
A. D Dick, V. Sharma, and J. Liversidge
Single dose intranasal administration of retinal autoantigen generates a rapid accumulation and cell activation in draining lymph node and spleen: implications for tolerance therapy
Br. J. Ophthalmol., August 1, 2001; 85(8): 1001 - 1006.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Ophthalmol.Home page
H.-R. Jiang, N. Taylor, L. Duncan, A. D Dick, and J. V Forrester
Total dose and frequency of administration critically affect success of nasal mucosal tolerance induction
Br. J. Ophthalmol., June 1, 2001; 85(6): 739 - 744.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
C. Broderick, L. Duncan, N. Taylor, and A. D. Dick
IFN-{gamma} and LPS-Mediated IL-10-Dependent Suppression of Retinal Microglial Activation
Invest. Ophthalmol. Vis. Sci., August 1, 2000; 41(9): 2613 - 2622.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 1999 by the BMJ Publishing Group Ltd.