The immune modulator FYT720 prevents autoimmune diabetes in nonobese diabetic mice

被引:57
作者
Yang, ZD
Chen, M
Fialkow, LB
Ellett, JD
Wu, RP
Brinkmann, V
Nadler, JL
Lynch, KR
机构
[1] Univ Virginia, Dept Internal Med, Charlottesville, VA 22908 USA
[2] Nova Pharma AG Transplantat Res, CH-4002 Basel, Switzerland
[3] Univ Virginia, Dept Pharmacol, Charlottesville, VA 22908 USA
关键词
FTY720; autoimmune diabetes; NOD mice; insulitis; lymphocytes;
D O I
10.1016/S1521-6616(02)00054-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
FrY720 is a novel immune regulatory drug derived from the fungal sphingosine analog ISP-1 (myriocin). FTY720 causes a redistribution of lymphocytes from circulation to secondary lymphoid tissues. Type I diabetes is an autoimmune disorder caused by cellular-mediated destruction of insulin-producing pancreatic 0 cells in the islets of Langerhans. Indeed, local infiltration of islets by mononuclear cells is the hallmark of Type 1 diabetes. Based on both FTY720's action and the involvement of cellular infiltration in the disease progression, we tested FTY720 for its ability to prevent autoimmune diabetes in diabetes-prone, nonobese diabetic (NOD) mice. We found that treatment with FrY720 completely prevented NOD mice from developing autoimmune diabetes. The FTY720-treated animals showed both reduced numbers of circulating lymphocytes and sharply diminished cellular infiltration of pancreatic islets. These results suggest that FrY720 may be effective in prevention of autoimmune diabetes or in slowing its progression. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:30 / 35
页数:6
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