scholarly journals Phenotype of regulatory T cells in human type 1 diabetes at diagnosis and partial remission phase

2015 ◽  
Vol 7 (S1) ◽  
Author(s):  
Daniela da Silva Camilo ◽  
Adriel Santos Moraes ◽  
Fernando Pradella ◽  
Paula Giovana Russini ◽  
Alliny Carolina Dionete Lima ◽  
...  
2017 ◽  
Vol 17 (10) ◽  
Author(s):  
Sally C. Kent ◽  
Stuart I. Mannering ◽  
Aaron W. Michels ◽  
Jenny Aurielle B. Babon

2006 ◽  
Vol 119 ◽  
pp. S166
Author(s):  
Tihamer Orban ◽  
Janos Kis ◽  
Peter Engelmann ◽  
Laszlo Szereday ◽  
Geoffrey Richman ◽  
...  

2020 ◽  
Vol 105 (6) ◽  
pp. 1947-1956 ◽  
Author(s):  
Xia Li ◽  
Ting Zhong ◽  
Rong Tang ◽  
Chao Wu ◽  
Yuting Xie ◽  
...  

Abstract Context Partial remission (PR) in type 1 diabetes (T1D) is accompanied by downregulation of the immune response. Programmed cell death-1 (PD-1) and its ligand (PD-L1) are important immunosuppressive molecules, but their changes in the PR phase are unclear. Objective We investigated the dynamic changes of PD-1/PD-L1 expression on T cells around the PR phase in T1D. Methods Ninety-eight T1D patients were recruited cross-sectionally and grouped according to PR status into nonremitters (individuals who did not undergo PR during the disease course; n = 39), pre-PR (n = 15), mid-PR (n = 30), and post-PR (n = 14) subgroups. PR was defined according to C-peptide level ≥300 pmol/L or index of insulin-adjusted hemoglobin A1c ≤9 as recommended. Among all the 98 patients, 29 newly diagnosed individuals were prospectively followed up for 1 year. The dynamic changes of PD-1/PD-L1 expression, frequency of regulatory T cells (Tregs) and IL-35+ Tregs among peripheral CD4/CD8+ T cells were determined. Results PD-1/PD-L1 on CD4+/CD8+ T cells showed a dynamic change around the PR phase: lowest in pre-PR phase, restored in mid-PR phase, and declined again in post-PR phase. Conversely, this pattern did not occur for nonremitters. Notably, PD-1 expression on CD8+ T cells in mid-PR was positively correlated with the length of the PR phase. The percentages of circulating Tregs and IL-35+ Tregs showed no relation to PR. Conclusions The PR phase is associated with restoration of PD-1/PD-L1 on CD4+ and CD8+ T cells, suggesting that PD-1/PD-L1 may be a potential target for prolonging this phase in T1D.


Diabetes ◽  
2008 ◽  
Vol 58 (2) ◽  
pp. 394-402 ◽  
Author(s):  
A. Toma ◽  
T. Laika ◽  
S. Haddouk ◽  
S. Luce ◽  
J.-P. Briand ◽  
...  

2004 ◽  
Vol 24 (4) ◽  
pp. 327-339 ◽  
Author(s):  
Patrick A. Ott ◽  
Marcus T. Dittrich ◽  
Bernhard A. Herzog ◽  
Robert Guerkov ◽  
Peter A. Gottlieb ◽  
...  

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Jing Chen ◽  
Anna V. Chernatynskaya ◽  
Jian-Wei Li ◽  
Matthew R. Kimbrell ◽  
Richard J. Cassidy ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Christine Bender ◽  
Sakthi Rajendran ◽  
Matthias G. von Herrath

Since the establishment of the network for pancreatic organ donors with diabetes (nPOD), we have gained unprecedented insight into the pathology of human type 1 diabetes. Many of the pre-existing “dogmas”, mostly derived from studies of animal models and sometimes limited human samples, have to be revised now. For example, we have learned that autoreactive CD8 T cells are present even in healthy individuals within the exocrine pancreas. Furthermore, their “attraction” to islets probably relies on beta-cell intrinsic events, such as the over-expression of MHC class I and resulting presentation of autoantigens such as (prepro)insulin. In addition, we are discovering other signs of beta-cell dysfunction, possibly at least in part due to stress, such as the over-expression of certain cytokines. This review summarizes the latest developments focusing on cytokines and autoreactive CD8 T cells in human type 1 diabetes pathogenesis.


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