scholarly journals Partial exhaustion of CD8 T cells and clinical response to teplizumab in new-onset type 1 diabetes

2016 ◽  
Vol 1 (5) ◽  
pp. eaai7793-eaai7793 ◽  
Author(s):  
S. A. Long ◽  
J. Thorpe ◽  
H. A. DeBerg ◽  
V. Gersuk ◽  
J. A. Eddy ◽  
...  
2018 ◽  
Vol 20 (4) ◽  
pp. 293-307 ◽  
Author(s):  
Peter S. Linsley ◽  
Carla J. Greenbaum ◽  
Mario Rosasco ◽  
Scott Presnell ◽  
Kevan C. Herold ◽  
...  

Diabetes ◽  
2018 ◽  
Vol 67 (11) ◽  
pp. 2319-2328
Author(s):  
Kaitlin R. Carroll ◽  
Eileen E. Elfers ◽  
Joseph J. Stevens ◽  
Jonathan P. McNally ◽  
David A. Hildeman ◽  
...  

2021 ◽  
Author(s):  
Ada Admin ◽  
Teresa Rodriguez-Calvo ◽  
Lars Krogvold ◽  
Natalie Amirian ◽  
Knut Dahl-Jørgensen ◽  
...  

In type 1 diabetes, a lifelong autoimmune disease, T cells infiltrate the islets and the exocrine pancreas in high numbers. CD8+ T cells are the main cell type found in the insulitic lesion, and CD8+ T cells reactive against beta cell antigens have been detected in the periphery and in the pancreas of subjects with short and long disease duration. The Diabetes Virus Detection (DiViD) study collected pancreatic tissue, by pancreatic tail resection, from living patients with recent-onset type 1 diabetes. These tissues have been extensively studied by the scientific community, but the autoreactive nature of the T cell infiltrate has remained unexplored. Our objective was to determine the number and localization of these cells in pancreas samples obtained through the DiViD study. Here, we demonstrate the presence of high frequencies of CD8+ T cells reactive against a highly relevant epitope derived from the preproinsulin signal peptide in pancreatic tissue samples from these donors. We additionally show the heterogeneity of islet distribution and CD8+ T cell infiltration. Our findings contribute to the current limited existing knowledge on T cell reactivity in the pancreas of recent onset type 1 diabetic donors, and indicate that antigen-specific therapies directed towards preproinsulin could have high clinical impact.


2017 ◽  
Vol 19 (1) ◽  
pp. 68-79 ◽  
Author(s):  
Mahinder Paul ◽  
Darshan Badal ◽  
Neenu Jacob ◽  
Devi Dayal ◽  
Rakesh Kumar ◽  
...  

2017 ◽  
Vol 187 (3) ◽  
pp. 581-588 ◽  
Author(s):  
Enida Kuric ◽  
Peter Seiron ◽  
Lars Krogvold ◽  
Bjørn Edwin ◽  
Trond Buanes ◽  
...  

2015 ◽  
Vol 13 (3) ◽  
pp. 56-57
Author(s):  
Mark R. Rigby ◽  
Kristina M. Harris ◽  
Ashley Pinckney ◽  
Linda A. Dimeglio ◽  
Marc S. Rendell ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (9) ◽  
pp. e0183887 ◽  
Author(s):  
Hector M. Granados ◽  
Andrew Draghi ◽  
Naomi Tsurutani ◽  
Kyle Wright ◽  
Marina L. Fernandez ◽  
...  

2013 ◽  
Vol 1 (4) ◽  
pp. 284-294 ◽  
Author(s):  
Mark R Rigby ◽  
Linda A DiMeglio ◽  
Marc S Rendell ◽  
Eric I Felner ◽  
Jean M Dostou ◽  
...  

2010 ◽  
Vol 185 (7) ◽  
pp. 3814-3818 ◽  
Author(s):  
Ashish K. Marwaha ◽  
Sarah Q. Crome ◽  
Constadina Panagiotopoulos ◽  
Kyra B. Berg ◽  
Huilian Qin ◽  
...  

2021 ◽  
Author(s):  
Ada Admin ◽  
Teresa Rodriguez-Calvo ◽  
Lars Krogvold ◽  
Natalie Amirian ◽  
Knut Dahl-Jørgensen ◽  
...  

In type 1 diabetes, a lifelong autoimmune disease, T cells infiltrate the islets and the exocrine pancreas in high numbers. CD8+ T cells are the main cell type found in the insulitic lesion, and CD8+ T cells reactive against beta cell antigens have been detected in the periphery and in the pancreas of subjects with short and long disease duration. The Diabetes Virus Detection (DiViD) study collected pancreatic tissue, by pancreatic tail resection, from living patients with recent-onset type 1 diabetes. These tissues have been extensively studied by the scientific community, but the autoreactive nature of the T cell infiltrate has remained unexplored. Our objective was to determine the number and localization of these cells in pancreas samples obtained through the DiViD study. Here, we demonstrate the presence of high frequencies of CD8+ T cells reactive against a highly relevant epitope derived from the preproinsulin signal peptide in pancreatic tissue samples from these donors. We additionally show the heterogeneity of islet distribution and CD8+ T cell infiltration. Our findings contribute to the current limited existing knowledge on T cell reactivity in the pancreas of recent onset type 1 diabetic donors, and indicate that antigen-specific therapies directed towards preproinsulin could have high clinical impact.


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