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A viral epitope that mimics a self antigen can accelerate but not initiate autoimmune diabetes
Urs Christen, … , Michael B.A. Oldstone, Matthias G. von Herrath
Urs Christen, … , Michael B.A. Oldstone, Matthias G. von Herrath
Published November 1, 2004
Citation Information: J Clin Invest. 2004;114(9):1290-1298. https://doi.org/10.1172/JCI22557.
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Article Autoimmunity

A viral epitope that mimics a self antigen can accelerate but not initiate autoimmune diabetes

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Abstract

We document here that infection of prediabetic mice with a virus expressing an H-2Kb–restricted mimic ligand to a self epitope present on β cells accelerates the development of autoimmune diabetes. Immunization with the mimic ligand expanded autoreactive T cell populations, which was followed by their trafficking to the islets, as visualized in situ by tetramer staining. In contrast, the mimic ligand did not generate sufficient autoreactive T cells in naive mice to initiate disease. Diabetes acceleration did not occur in H-2Kb–deficient mice or in mice tolerized to the mimic ligand. Thus, arenavirus-expressed mimics of self antigens accelerate a previously established autoimmune process. Sequential heterologous viral infections might therefore act in concert to precipitate clinical autoimmune disease, even if single exposure to a viral mimic does not always cause sufficient tissue destruction.

Authors

Urs Christen, Kurt H. Edelmann, Dorian B. McGavern, Tom Wolfe, Bryan Coon, Meghann K. Teague, Stephen D. Miller, Michael B.A. Oldstone, Matthias G. von Herrath

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Figure 2

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CD8 T cell populations specific for the mimicking epitope PV-NP205 are s...
CD8 T cell populations specific for the mimicking epitope PV-NP205 are significantly expanded after sequential infection with PV. (A and B) RIP-LCMV-NP and RIP-LCMV-NP × Kb(–) mice were infected with 105 PFU LCMV or PV. After 4 weeks, the mice received a secondary infection of either LCMV or PV. (A) Intracellular cytokine staining (ICCS) after stimulation with PV-NP205 is displayed for 1 representative mouse infected first with LCMV (LCMV alone) and then with PV (LCMV-PV) (mean frequencies are indicated in boxed areas). (B) The frequency of epitope-specific CD8 T cells in the blood was determined by ICCS for IFN-γ after stimulation with the indicated peptides (key) immediately before (upper panel) and 7 days after (lower panel) secondary infection. (C) Numbers of H-2Kb–restricted PV-NP205–specific lymphocytes after LCMV or PV infection, assessed by ICCS for IFN-γ. Splenocytes were harvested on day 35 from mice that received LCMV at day 0 (d0) and, for the PV group, PV at day 28 (d28). Means (± SEM) are displayed. (D) Lytic precursors after LCMV-NP396 versus PV-NP205 antigenic stimulation for 10 days. In addition to lytic activity, IFN-γ production was assessed in the supernatant of each well; wells with IFN-γ levels of more than 0.05 ng/ml by ELISA were counted as positive. IFN-γ production was on average 13 (± 3.5) ng/ml in LCMV-NP396–stimulated cultures and 7.1 (± 3.1) ng/ml in PV-NP205–stimulated cultures. This experiment was repeated three times and mean values (± SEM) are displayed. *P < 0.05.

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