Oral administration of PDX1 confers protection against insulitis in the non-obese diabetic (NOD) mice

被引:2
作者
Lin, Peng [1 ]
Li, Wenjuan [1 ]
Yao, Zhina [2 ]
Sun, Yu [1 ]
Wang, Lingshu [1 ]
Li, Shiwu [3 ]
Chen, Li [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Endocrine, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Hosp Reprod Med, Jinan 250012, Shandong, Peoples R China
[3] Univ Florida, Coll Med, Dept Pathol Immunol & Lab Med, Gainesville, FL USA
基金
中国国家自然科学基金;
关键词
Type; 1; diabetes; Immunotherapy; NOD mice; Insulitis; PDX1; NATURAL-HISTORY; TYPE-1; MELLITUS; PREVENTION; STRATEGIES; LESSONS; DISEASE; CELLS;
D O I
10.1016/j.bbrc.2015.09.098
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type 1 diabetes is a T cell-mediated organ-specific autoimmune disease. Antigen-specific immune intervention allows the selective targeting of autoreactive T cell, while leaving the remainder of the immune system intact. However, immune intervention for type 1 diabetes has not yielded perfect results clinically. In our paper published previously, we asked whether pancreatic duodenal home box 1 (PDX1) is a target of anti-islet autoimmunity in type 1 diabetes. In this experiment, we assessed the therapeutic effect of oral administration of PDX1 on diabetes development of 4-week-old non-obese diabetic (NOD) mice. The results indicate that PDX1 immunization is an effective intervention strategy for delaying the onset of diabetes in NOD mice in association with: 1) reduced insulitis; 2) suppression of destructive autoreactive T cells; 3) augmentation of regulatory T cells; 4) a shift in cytokine production. The present observations suggest that immunization with PDX1 modulates immune cell responses in NOD mice, raising the possibility that it is beneficial in ameliorating autoimmune destruction of beta-cells and delaying type I diabetes development clinically. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:656 / 663
页数:8
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