Differential cytokine expression detected by protein microarray screening in peripheral blood of patients with refractory Graves' disease

作者：Song, Rong-hua; Qin, Qiu; Wang, Xuan; Yan, Ni; Meng, Shuai; Shi, Xiao-hong; He, Shuang-tao; Zhang, Jin-an^*

来源：Clinical Endocrinology, 2016, 84(3): 402-407.

DOI：10.1111/cen.12778

• AUTOIMMUNE THYROID-DISEASE
• GENE POLYMORPHISMS
• IFN-GAMMA
• TNF-ALPHA
• ASSOCIATION
• CELL
• INTRACTABILITY
• THYROGLOBULIN
• RECEPTOR
• HYPERTHYROIDISM

ObjectiveThe prognosis of Graves' disease (GD) varies among patients. However, the immune pathogenesis of refractory GD is still unknown. The aim of this study was to explore the cytokine expression profile associated with refractory GD. @@@ MethodsPreliminary cytokine protein microarray screening was performed to detect differentially expressed cytokines in the plasma of four patients with refractory GD and four patients with stable GD. Some differentially expressed cytokines were then validated in plasma by enzyme-linked immunosorbent assay (ELISA) and in peripheral blood mononuclear cells (PBMCs) by quantitative real-time polymerase chain reaction (qRT-PCR) on another independent set of samples. @@@ ResultsWe found that 21 cytokines were differentially expressed between patients with intractable GD and those in remission, including 18 upregulated and 3 downregulated cytokines with a fold change >130 and <077, respectively. Intractability-related elevation of three cytokines (IL-4, IL-6 and IL-10) was validated by ELISA in plasma on another GD cohort with 30 patients in recurrence and 14 in remission (t-test, P=0035, 0033 and 0041, respectively). Furthermore, mRNA expression of IL-4, IL-6 and IL-10 in PBMCs, detected by qRT-PCR, was significantly elevated in patients with refractory GD compared with those in remission (P=0039, 0047 and 0042, respectively). @@@ ConclusionThe severity of GD is associated with the aberrant expression and secretion of several cytokines that may serve as potential biomarkers and predictors for disease prognosis. Targeting these cytokines or their receptors may also lead to a novel therapeutic intervention for GD.

• 出版日期2016-3
• 单位复旦大学