Inhibition of autoimmune diabetes by Fas ligand: The paradox is solved

Sunshin Kim, Kyoung Ah Kim, Dae Youn Hwang, Tae H. Lee, Nobuhiko Kayagaki, Hideo Yagita, Myung Shik Lee

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85 Citations (Scopus)


Previous reports that diabetogenic lymphocytes did not induce diabetes in nonobese diabetic (NOD)-lpr mice suggested the critical role of Fas-Fas ligand (FasL) interaction in pancreatic β cell apoptosis. However, recent works demonstrated that FasL is not an effector molecule in islet β cell death. We addressed why diabetes cannot be transferred to NOD-lpr mice despite the nonessential role of Fas in β cell apoptosis. Lymphocytes from NOD-lpr mice were constitutively expressing FasL. A decrease in the number of FasL+ lymphocytes by neonatal thymectomy facilitated the development of insulitis. Cotransfer of FasL+ lymphocytes from NOD-lpr mice completely abrogated diabetes after adoptive transfer of lymphocytes from diabetic NOD mice. The inhibition of diabetes by cotransferred lymphocytes was reversed by anti-FasL Ab, indicating that FasL on abnormal lymphocytes from NOD-lpr mice was responsible for the inhibition of diabetes transfer. Pretreatment of lymphocytes with soluble FasL (sFasL) also inhibited diabetes transfer, sFasL treatment decreased the number of CD4+CD45RB(low) cells and increased the number of propidium iodide-stained cells among CD4+CD45RB(low) cells, suggesting that sFasL induces apoptosis on CD4+CD45RB(low) 'memory' cells. These results resolve the paradox between previous findings and suggest a new role for FasL in the treatment of autoimmune disorders. Our data also suggest that sFasL is involved in the deletion of potentially hazardous peripheral 'memory' cells, contrary to previous reports that Fas on unmanipulated peripheral lymphocytes is nonfunctional.

Original languageEnglish
Pages (from-to)2931-2936
Number of pages6
JournalJournal of Immunology
Issue number6
Publication statusPublished - 2000 Mar 15

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology


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