4.7 Article

Where CD4+ CD25+ T reg cells impinge on autoimmune diabetes

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JOURNAL OF EXPERIMENTAL MEDICINE
卷 202, 期 10, 页码 1387-1397

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ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20051409

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  1. NIAID NIH HHS [P01 AI039671, P01-AI139671-09] Funding Source: Medline

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Foxp3 is required for the generation and activity of CD4(+)CD25(+) regulatory T (T reg) cells, which are important controllers of autoimmunity, including type-1 diabetes. To determine where T reg cells affect the diabetogenic cascade, we crossed the Foxp3 scurfy mutation, which eliminates T reg cells, with the BDC2.5 T cell receptor ( TCR) transgenic mouse line. In this model, the absence of T reg cells did not augment the initial activation or phenotypic characteristics of effector T cells in the draining lymph nodes, nor accelerate the onset of T cell infiltration of the pancreatic islets. However, this insulitis was immediately destructive, causing a dramatic progression to overt diabetes. Microarray analysis revealed that T reg cells in the insulitic lesion adopted a gene expression program different from that in lymph nodes, whereas T reg cells in draining or irrelevant lymph nodes appeared very similar. Thus, T reg cells primarily impinge on autoimmune diabetes by reining in destructive T cells inside the islets, more than during the initial activation in the draining lymph nodes.

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