Serum levels of cytokines are not suitable to monitor

Our results demonstrate only an 1.Carsalam 5-fold increase in IL-6 levels in patients with CLBP, which could even occur after physical activity or in Bifonazole obesity. However, the relevance of cytokine measurements should generally be regarded with caution as serum levels of most cytokines are influenced by a complex interplay of macrophages/monocytes, fibroblasts, endothelial2/epithelial cells and dendritic cells thus complicating the extrapolation from plasma cytokines to immune cell functions. Moreover, ranges of detection exhibits considerable variances between the different assays used. Even different types of Luminex-based platforms exhibit differences in their ability to measure serum levels of cytokines and thus, may be more useful in studies in which relative rather than absolute changes in cytokines are of interest. Overall, these data suggest that serum levels of cytokines are not suitable to monitor the adaptive immune response in CLBP and prompted us to analyze the expression of cytokines directly in the compartment of CD4 + cells as central players of the T cell response. While no differences in the expression of TH1 and TH2 cytokines were observed, qPCR results clearly pointed to an increased abundance of Tregs in CLBP patients, as expression of both TGF-b and the transcription factor FoxP3 were significantly increased. Moreover, expression of IL-23 was clearly decreased supporting the assumption that TH17 frequency may be reduced. IL-17 and RORcT, however, did not differ significantly between CLBP and controls which may be due to the fact that the subset of TH17 cells per se is only less than 2% of CD4+ cells. Thus, resolving differences of cytokine expression without prior cell sorting may be difficult. The opposite results of increased IL-23 protein levels and decreased IL23-mRNA-expression is in line with a wide body of literature showing a big discrepancy between mRNA expression and protein levels as a result of control mechanisms. These can affect post-transcriptional, translational and protein degrading processes.

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