Islet-cell antigen-reactive T cells show different expansion rates and Th1/Th2 differentiation in type 1 diabetic patients and healthy controls

2005 ◽  
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pp. 102-114 ◽  
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B HERZOG ◽  
S QUAST ◽  
H HOFSTETTER ◽  
B BOEHM ◽  
...  
PLoS ONE ◽  
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Adolfo Pacifico ◽  
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Diabetes ◽  
2009 ◽  
Vol 58 (10) ◽  
pp. 2267-2276 ◽  
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R. Hilbrands ◽  
V. A.L. Huurman ◽  
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J. H.L. Velthuis ◽  
M. De Waele ◽  
...  

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Vol 2014 ◽  
pp. 1-7 ◽  
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Mina Tabrizi ◽  
Farzaneh Abbasi ◽  
Asal Ataie-Jafari ◽  
Behrouz Nikbin ◽  
...  

Type 1 diabetes is recognized as an autoimmune inflammatory disease and low grade inflammation is also observed in type 2 diabetic patients. Interleukin 17 (IL-17) is a new player in inflammation. Th17 cells, as the main source of IL-17, require transforming growth factorβ(TGF-β) and interleukin 23 (IL-23). The aim of this study was to investigate serum IL-17, IL-23 and TGF-βlevels in diabetic patients and controls. In this case-control study, serum levels of IL-17, IL-23, and TGF-βwere measured in 24 type 1 diabetic patients and 30 healthy controls using the ELISA method. Simultaneously, the same methodology was used to compare serum concentration of these three cytokines in 38 type 2 diabetic patients and 40 healthy controls. There was no significant difference between serum levels of IL-17 and IL-23 cytokines between cases and controls. However, TGF-βwas significantly lower in type 1 diabetic patients (P<0.001). Serum IL-17 and IL-23 levels demonstrate no association with type 1 and type 2 diabetes, but, in line with previous studies, TGF-βlevels were lower in type 1 diabetic patients.


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