Article ID Journal Published Year Pages File Type
2564843 Progress in Neuro-Psychopharmacology and Biological Psychiatry 2014 5 Pages PDF
Abstract

•At baseline, the proportion of Th17 cells was higher in the patient group.•At baseline, the levels of IFN-γ and IL-6 were higher in the patient group.•After treatment, the proportion of Th17 cells decreased significantly.•The PANSS total score correlated positively with the levels of Th17 cells.

ObjectiveThe present study was to examine the role of pro-inflammatory T helper 17 (Th17) cells in drug naïve, first episode schizophrenia.MethodPatients with normal weight, drug naïve, first episode schizophrenia and healthy controls were enrolled in the study. Flow cytometric analysis was performed to analyze the proportion of Th17 cells among the CD4+ T cells. Plasma levels of interleukin-17 (IL-17), interferon-γ (IFN-γ) and interleukin-6 (IL-6) were examined using enzyme-linked immunosorbent assay (ELISA). Psychopathology was assessed using the Positive and Negative Syndrome Scale (PANSS). All measures were repeated for the patient group after 4 weeks of risperidone treatment.ResultsSixty-nine patients with normal weight, drug naïve, first episode schizophrenia and 60 healthy controls were enrolled. At baseline, the patient group hadz significantly higher proportions of Th17 cells and plasma levels of IFN-γ and IL-6 compared with the control group (p's < 0.01). Within the patient group, there were significant positive relationships between the proportion of Th17 cells, plasma levels of IL-17, IFN-γ, IL-6 and the PANSS total score after controlling for potential confounding variables (p's < 0.05). After 4 weeks of risperidone treatment, the proportion of Th17 cells decreased significantly (p < 0.001), and there was a significant positive relationship between the PANSS total score change rate and the change in proportion of Th17 cells (p = 0.039).ConclusionsPatients with normal weight, drug naïve, first episode schizophrenia present activation of Th17 cells, which might be associated with therapeutic response after risperidone treatment.

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Life Sciences Neuroscience Biological Psychiatry
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