Kazem Ahmadi1, Majid Riazipour. 1. Research Center of Molecular Biology, Baqiyatallah University of Medical Sciences, Tehran, Iran. kazahmadi@yahoo.com
Abstract
BACKGROUND: T-2 toxin is a mycotoxin of type A trichothecenes produced by several fungal genera such as Fusarium species. Mycotoxins can affect both cell mediated and humoral immune compartments. OBJECTIVE: The purpose of this study was to investigate the effect of T-2 toxin on cytokine production by mouse peritoneal macrophages and lymph node T cells. METHODS: Mouse peritoneal macrophages and lymph node T cells were isolated and treated with different concentrations of T-2 toxin and incubated at 370C and 5% CO2 in air for 48 hours. Cell free media were removed and used for cytokine assay by an ELISA method. RESULTS: T-2 toxin significantly reduced IL-1beta release in a concentration dependent manner (p<0.005, p<0.001). Interleukin-12 and TNF-alpha production were significantly increased in response to 0.001ng/ml, 0.01ng/ml and 0.1ng/ml of T-2 toxin (p<0.001). However, T-2 toxin at higher concentrations ranging from 1ng/ml to 100ng/ml, reduced both IL-12 (p<0.001) and TNF-alpha production (p<0.005, p<0.05). The effects of T-2 toxin on lymph node T cells showed that IL-4 and IL-10 release was decreased in a concentration dependent manner (all with p<0.01). T-2 toxin at concentrations between 1ng/ml and 100ng/ml reduced the release of both IL-2 and IFN-gamma (p<0.05, p<0.001). CONCLUSION: The results suggest that T-2 toxin at low concentrations can highly induce secretion of IL-12, TNF-alpha, IFN-gamma and IL-2 and it may be used as a positive immunomodulator in the human model.
BACKGROUND:T-2 toxin is a mycotoxin of type A trichothecenes produced by several fungal genera such as Fusarium species. Mycotoxins can affect both cell mediated and humoral immune compartments. OBJECTIVE: The purpose of this study was to investigate the effect of T-2 toxin on cytokine production by mouse peritoneal macrophages and lymph node T cells. METHODS:Mouse peritoneal macrophages and lymph node T cells were isolated and treated with different concentrations of T-2 toxin and incubated at 370C and 5% CO2 in air for 48 hours. Cell free media were removed and used for cytokine assay by an ELISA method. RESULTS:T-2 toxin significantly reduced IL-1beta release in a concentration dependent manner (p<0.005, p<0.001). Interleukin-12 and TNF-alpha production were significantly increased in response to 0.001ng/ml, 0.01ng/ml and 0.1ng/ml of T-2 toxin (p<0.001). However, T-2 toxin at higher concentrations ranging from 1ng/ml to 100ng/ml, reduced both IL-12 (p<0.001) and TNF-alpha production (p<0.005, p<0.05). The effects of T-2 toxin on lymph node T cells showed that IL-4 and IL-10 release was decreased in a concentration dependent manner (all with p<0.01). T-2 toxin at concentrations between 1ng/ml and 100ng/ml reduced the release of both IL-2 and IFN-gamma (p<0.05, p<0.001). CONCLUSION: The results suggest that T-2 toxin at low concentrations can highly induce secretion of IL-12, TNF-alpha, IFN-gamma and IL-2 and it may be used as a positive immunomodulator in the human model.