کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6087125 | 1207349 | 2015 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Adult-onset type 1 diabetes patients display decreased IGRP-specific Tr1 cells in blood Adult-onset type 1 diabetes patients display decreased IGRP-specific Tr1 cells in blood](/preview/png/6087125.png)
- IGRP-specific CD4+ T cell responses is distinct between T1D and healthy.
- Decreased IGRP-specific Tr1 cells contribute to the onset of adult-onset T1D.
- The pathogenesis of adult- and juvenile-onset T1D is not completely identical.
The breakdown of immune tolerance against islet antigens causes type 1 diabetes (T1D). The antigens associated with adult-onset T1D (AT1D) remain largely undefined. It is possible that AT1D patients display a unique type of CD4+ T cells specific for a certain islet antigen. Here we analyzed the cytokine production profiles of CD4+ helper T (Th) cells that are specific for three islet antigens; GAD65, preproinsulin, and IGRP in patients with AT1D, juvenile-onset T1D (JT1D), and age-, gender- and human leukocyte antigen (HLA)-matched control adults. While IGRP-specific Th cells in AT1D patients were dominantly Th1 cells, IGRP-specific Th cells in control adults and JT1D patients were dominantly Th2 and T regulatory type 1 (Tr1) cells. Notably, the frequency of IGRP-specific Tr1 cells was significantly lower in AT1D patients than in control adults and JT1D patients. In conclusion, our study suggests that IGRP-specific Th cells play a unique pathogenic role in AT1D.
Journal: Clinical Immunology - Volume 161, Issue 2, December 2015, Pages 270-277