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Identifying the Cells Breaching Self-Tolerance in Autoimmunity
Author(s) -
Robert A. Benson,
Agapitos Patakas,
Paola Conigliaro,
C. M. Rush,
Paul Garside,
Iain B. McInnes,
James M. Brewer
Publication year - 2010
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.0903951
Subject(s) - autoimmunity , immunology , self tolerance , disease , phenotype , clonal deletion , autoimmune disease , function (biology) , immune tolerance , medicine , biology , t cell , microbiology and biotechnology , immune system , antibody , genetics , t cell receptor , pathology , gene
Activation of auto-reactive T cells by activated dendritic cells (DCs) presenting self-Ag is widely assumed to be the precipitating event in the development of autoimmune disease. However, despite such widely held preconceptions, supporting data are scarce and subjective, particularly in experimental arthropathy. We have adapted a novel murine model of breach of self-tolerance allowing evaluation of the contribution of endogenous DCs to the development of autoimmune responses and disease. For the first time, we reveal the critical role played by conventional DCs, and the timing and location of this process. We further demonstrate the importance of this finding by clinically relevant, therapeutic manipulation of conventional DC function, resulting in decreased autoimmune phenotype and disease severity.

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