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(American Journal of Pathology. 2006;169:2137-2147.)
© 2006 American Society for Investigative Pathology
DOI: 10.2353/ajpath.2006.060539

In CD4⁺ T-Cell-Induced Diabetes, Macrophages Are the Final Effector Cells that Mediate Islet ß-Cell Killing

Studies from an Acute Model

From the Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri

To understand better how diabetogenic CD4⁺ T cells induce islet ß-cell death and cause diabetes, a transfer model of acute diabetes using the diabetogenic CD4⁺ BDC2.5 T-cell clone was established. Transfer of activated BDC T cells into NOD.scid mice resulted in diabetes within a week, characterized by strong inflammatory reaction. Electron micrographs of pancreas depicted macrophages in close contact with ß cells that exhibited signs of apoptosis. Transfer into irradiated recipients inhibited inflammation and the development of diabetes, demonstrating an obligatory role for leukocytes. Selective depletion of neutrophils or natural killer cells had no effect on diabetes induced by BDC2.5 T cells. In contrast, in vivo depletion of phagocytic cells by injection of liposomes containing clodronate abolished diabetes, although inflammation remained present and was characterized mainly by neutrophil infiltration. Treatment with clodronate-liposomes did not affect the antigen-presenting cells within the pancreas. Last, activated macrophages isolated from infiltrated pancreas exhibited cytolytic activity toward primary islet ß cells. Taken together, these results demonstrate that activated macrophages are the key cells mediating islet ß-cell death induced by activated CD4⁺ T cells.

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