Promoting tolerance to proteolipid protein-induced experimental autoimmune encephalomyelitis through targeting dendritic cells

In T cell-mediated autoimmune diseases, self-reactive T cells with known antigen specificity appear to be particularly promising targets for antigen-specific induction of tolerance without compromising desired protective host immune responses. Several lines of evidence suggest that delivery of antig...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2010-10, Vol.107 (40), p.17280-17285
Hauptverfasser: Stern, Joel N. H., Keskin, Derin B., Kato, Zenichiro, Waldner, Hanspeter, Schallenberg, Sonja, Anderson, Ana, von Boehmer, Harald, Kretschmer, Karsten, Strominger, Jack L.
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Sprache:eng
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Zusammenfassung:In T cell-mediated autoimmune diseases, self-reactive T cells with known antigen specificity appear to be particularly promising targets for antigen-specific induction of tolerance without compromising desired protective host immune responses. Several lines of evidence suggest that delivery of antigens to antigen-presenting dendritic cells (DCs) in the steady state (i.e., to immature DCs) may represent a suitable approach to induce antigen-specific T-cell tolerance peripherally. Here, we report that anti-DEC205—mediated delivery of the self-peptide proteolipid protein (PLP)139-151 to DCs ameliorated clinical symptoms in the PLP-induced SJL model of experimental autoimmune encephalomyelitis. Splenocytes from treated mice were anergized to PLP139-151, and IL-17 secretion was markedly reduced. Moreover, we show directly, using transgenic CD4⁺ Vβ6⁺ TCR T cells specific for PLP139-151, that, under the conditions of the present experiments, these cells also became anergic. In addition, evidence for a CD4⁺ T cell-mediated suppressor mechanism was obtained.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1010263107