articleThe Journal of Experimental MedicineJun 7, 2004BRONZE OA

CD25+ CD4+ T Cells, Expanded with Dendritic Cells Presenting a Single Autoantigenic Peptide, Suppress Autoimmune Diabetes

Rockefeller University

PubMed
Indexed incrossrefpubmed

Abstract

In the nonobese diabetic (NOD) mouse model of type 1 diabetes, the immune system recognizes many autoantigens expressed in pancreatic islet beta cells. To silence autoimmunity, we used dendritic cells (DCs) from NOD mice to expand CD25+ CD4+ suppressor T cells from BDC2.5 mice, which are specific for a single islet autoantigen. The expanded T cells were more suppressive in vitro than their freshly isolated counterparts, indicating that DCs from autoimmune mice can increase the number and function of antigen-specific, CD25+ CD4+ regulatory T cells. Importantly, only 5,000 expanded CD25+ CD4+ BDC2.5 T cells could block autoimmunity caused by diabetogenic T cells in NOD mice, whereas 10(5) polyclonal, CD25+ CD4+…

Citation impact

728
total citations
FWCI
24.04
Percentile
100%
References
57
Citations per year

Authors

5

Topics & keywords

Keywords
  • IL-2 receptor
  • NOD mice
  • Insulitis
  • Interleukin 21
  • Biology
  • Autoimmunity
  • Immune system
  • Antigen-presenting cell
UN Sustainable Development Goals
  • Good health and well-being
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