| Literature DB >> 20644171 |
Jonathan D Katz1, Jennifer K Ondr, Robert J Opoka, Zacharias Garcia, Edith M Janssen.
Abstract
In type 1 diabetes, the breach of central and peripheral tolerance results in autoreactive T cells that destroy insulin-producing, pancreatic beta cells. In this study, we identify a critical subpopulation of dendritic cells responsible for mediating both the cross-presentation of islet Ags to CD8(+) T cells and the direct presentation of beta cell Ags to CD4(+) T cells. These cells, termed merocytic dendritic cells (mcDCs), are more numerous in the NOD mouse and, when Ag-loaded, rescue CD8(+) T cells from peripheral anergy and deletion while stimulating islet-reactive CD4(+) T cells. When purified from the pancreatic lymph nodes of overtly diabetic NOD mice, mcDCs break peripheral T cell tolerance to beta cells in vivo and induce rapid onset type 1 diabetes in the young NOD mouse. Thus, the mcDC subset appears to represent the long-sought APC responsible for breaking peripheral tolerance to beta cell Ags in vivo.Entities:
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Year: 2010 PMID: 20644171 PMCID: PMC2916973 DOI: 10.4049/jimmunol.1001398
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422