Amelioration of diabetes in nonobese diabetic mice with advanced disease by linomide-induced immunoregulation combined with Reg protein treatment

被引:71
作者
Gross, DJ
Weiss, L
Reibstein, I
van den Brand, J
Okamoto, H
Clark, A
Slavin, S
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Endocrinol & Metab, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Bone Marrow Transplantat, IL-91120 Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Hadassah Med Ctr, Canc Immunobiol Lab, IL-91120 Jerusalem, Israel
[4] Tohoku Univ, Sch Med, Dept Biochem, Sendai, Miyagi 9877, Japan
[5] Radcliffe Infirm, Oxford Diabet Res Labs, Oxford OX2 6HE, England
基金
英国惠康基金;
关键词
D O I
10.1210/en.139.5.2369
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oral linomide, (quinoline-3-carboxamide), has been shown to prevent autoimmune insulitis, islet destruction, and diabetes in NOD mice treated at an early stage of the disease, but confers only partial protection in animals with advanced disease. Reg protein, the gene product of a complementary DNA isolated from a regenerating rat islet library, has been previously shown to induce expansion of beta-cell mass in pancreatectomized rats. To determine the effect of treatment combining immunomodulation and Reg protein on advanced autoimmune diabetes, we treated female NOD mice with oral linomide and ip Reg protein injections. In 18-week-old animals with less severe disease (glucose tolerant), treatment with each agent alone resulted in amelioration of diabetes, as did treatment with Reg alone in B-week-old prediabetic mice. In 14-week-old animals with more severe disease (glucose intolerant), only treatment;with the combination of both agents, but not that with each separately, resulted in amelioration of diabetes. Our study suggests that treatment aimed at abrogation of autoimmunity combined with expansion of p-cell mass constitutes a potential therapeutic approach for treatment of insulin-dependent diabetes mellitus.
引用
收藏
页码:2369 / 2374
页数:6
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