dendrtitic cell subsets in autoimmune diabetes

DEC-205是一种由独特的CD8 α +树突状细胞亚群表达的内吞受体。作为甘露糖受体家族的一员，DEC-205能内吞抗原，并允许它们在MHC I类和II类上呈现。在免疫正常小鼠中，通过嵌合抗体构建将蛋白靶向DEC-205可导致抗原特异性CD4+和CD8+ T细胞克隆性缺失或激活。最近的工作（Mukhopadhaya A, et al.）PNAS 2008)的研究表明，NOD小鼠（在12-15周龄左右发展为自身免疫性糖尿病）的β细胞特异性CD8+ T细胞可以被耗尽。我们现在正在评估DEC-205靶向在自身免疫性NOD小鼠中消耗或激活CD4+ T细胞的能力。

DEC-205 is an endocytic receptor expressed by a distinct CD8 alpha+ dendritic cell subpopulation. A member of the mannose receptor family, DEC-205 endocytoses antigens and allows them to be presented on MHC class I and II. Targeting of proteins to DEC-205 through chimeric antibody constructs causes clonal deletion or anergy of antigen-specific CD4+ and CD8+ T cells in immunologically normal mice. Recent work (Mukhopadhaya A, et al. PNAS 2008) has shown that beta cell-specific CD8+ T cells can be depleted from NOD mice (which develop autoimmune diabetes around 12-15 weeks of age). We are now assessing the ability of DEC-205 targeting to deplete or anergize CD4+ T cells in autoimmune NOD mice. NOD mice were injected with BDC2.5 T cell receptor (TCR) transgenic CD4+ T cells that recognize an unknown beta cell antigen, followed by treatment with anti-DEC-205 attached to a BDC mimeotope peptide. Three days after anti-DEC-205 treatment, BDC T cells had proliferated in the spleen, peripheral lymph nodes and pancreatic lymph nodes, similar to results in normal mice. However, ten days after treatment with anti-DEC-205, when T cells are deleted in normal mice, antigen-specific cells remained in the autoimmune mice and were not anergic (they retained capacity to produce interferon gamma). We first learned that neither antigen dose or endogenous TLRL were contributing to this lack of tolerance. We then found that if a mimetope peptide with a lower affinity for MHC class II was used, the BDC2.5 T cells exhibited a more tolerogenic phenotype. Another type of DC, Plasmacytoid DCs (pDC) have traditionally been identified as a distinct subset of DCs involved as an innate immune cell in viral immunity due to their expression of TLR7/TLR9 and their ability to secrete large amount of type 1 IFN upon stimulation. However, more recently, pDCs have also been shown to present antigen to CD4 T cells and to be vital in the induction of immune tolerance. We are now addressing the role of pDC in the pathogenesis of autoimmune diabetes by 1) studying the number of pDCs at different stages of diabetes progression in the NOD mice, and in non autoimmune strains. 2) understanding how diabetes susceptibility genes affect pDC development, focusing on genes found in the susceptibility loci Idd3 and Idd5. In the future, we will deplete pDCs in NOD mice and determine if this affects diabetes development.