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Serum IL-17, IL-23, and TGF-βLevels in Type 1 and Type 2 Diabetic Patients and Age-Matched Healthy Controls
Author(s) -
Azam Roohi,
Mina Tabrizi,
Farzaneh Abbasi,
Asal AtaieJafari,
Behrouz Nikbin,
Bagher Larijani,
Mostafa Qorbani,
Alipasha Meysamie,
Hossein AsgarianOmran,
Bahram Nikmanesh,
Arezou Bajouri,
Novin Shafiey,
Akram Maleki
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/718946
Subject(s) - type 2 diabetes , medicine , transforming growth factor , inflammation , interleukin 17 , type 1 diabetes , interleukin 23 , endocrinology , diabetes mellitus , interleukin , interleukin 6 , case control study , cytokine , immunology
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 factor β (TGF- β ) and interleukin 23 (IL-23). The aim of this study was to investigate serum IL-17, IL-23 and TGF- β levels in diabetic patients and controls. In this case-control study, serum levels of IL-17, IL-23, and TGF- β were 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- β was 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- β levels were lower in type 1 diabetic patients.

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