[Interferon-γ Induced by Toxoplasma gondii Excreted/Secreted Antigens Promotes Apoptosis of CD4+CD25+ Regulatory T Cells].

Ke Ge, Xiao-yan Qiu, Li-juan Wang, Hui Chen, Lu-yan Zhang, Jing-fan Qiu, Yong Wang
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Abstract

Objective: To investigate the effect of excreted/secreted antigens (ESAs) from Toxoplasma gondii RH strain and TgCtwh3 strain on apoptosis of CD4+CD25+ regulatory T cells and interferon-γ (IFN-γ) secretion.

Methods: ESAs of Toxoplasma gondii RH strain and TgCtwh3 strain were prepared. Splenic mononuclear cells were isolated from C57BL/6 mice and randomly divided into RH ESA group(2×106 cells/well with addition of 10 μg/ml RH ESA), TgCtwh3 ESA group (2×106 cells/well with addition of 10 μg/ml TgCtwh3 ESA) and control group(2×106 cells/well with addition of 10 μg/ml ovalbumin). Flow cytometry was performed to examine the early apoptosis of CD4+CD25+ regulatory T cells after treatment for 48 h and 72 h. ELISA was conducted to determine the level of IFN-γ in the supernatant after treatment for 72 h. In another experiment, the 3 groups of splenic mononuclear cells were added with 10 μg/ml anti-IFN-γ antibody for 72 h and flow cytometry was performed to examine the early apoptosis of CD4+CD25+ regulatory T cells. Meanwhile, splenic mononuclear cells from IFN-γ knockout and wild-type C57BL/6 mice were also divided into the above-described 3 groups, and flow cytometry was performed to examine the early apoptosis of CD4+CD25+ regulatory T cells after treatment for 72 h.

Results: The concentrations of RH ESA and TgCtwh3 ESA were 0.54 mg/ml and 2.14 mg/ml, respectively. Flow cytometry showed that the early apoptosis rate of CD4+CD25+ regulatory T cells in the RH ESA group and the TgCtwh3 ESA group after 48 h treatment was (12.90±1.26)% and (9.71±1.04)%, respectively (P<0.05), both significantly higher than that in control group (4.48±0.48)% (P<0.01) . The early apoptosis rate of CD4+CD25+ regulatory T cells after 72 h in the RH ESA group was(15.21±1.11)%, significantly higher than that in the TgCtwh3 ESA group[(11.02±0.92)%] (P<0.05) and the control group[(10.10±1.49)%](P<0.01). ELISA showed that the level of interferon-γ in the RH ESA group and the TgCtwh3 ESA group after 72 h was(4 764.0±118.7) pg/ml and (3 629.0±33.6) pg/ml, respectively (P<0.01), both significantly higher than that in the control[(679.4±30.6) pg/ml](P<0.01). Flow cytometry revealed lower early apoptosis rate of CD4+CD25+ regulatory T cells in the RH ESA group added with anti-IFN-γ antibody[(10.44±1.44)%] compared with that without the addition of the antibody[(14.96±0.83)](P<0.05). But this difference was not observed for the TgCtwh3 ESA group. Moreover, the RH ESA-induced apoptosis rate of regulatory T cells from IFN-γ knockout mice[(10.64±0.55)%] was significantly lower than that from the wild-type mice [(15.21±1.11)%](P<0.01). But this difference was not found for the TgCtwh3 ESA treatment.

Conclusion: T. gondii RH ESA induces apoptosis of CD4+CD25+ regulatory T cells and IFN-γ secretion, and these effects are stronger than those of TgCtwh3 ESA. The T. gondii ESA-induced IFN-γ stimulates generation of anti-Toxoplasma immunity during acute Toxoplasma infection through mediation of regulatory T cell apoptosis.

[弓形虫排泄/分泌抗原诱导的干扰素γ促进CD4+CD25+调节性T细胞凋亡]。
目的:探讨刚地弓形虫RH株和TgCtwh3株排泄/分泌抗原(ESAs)对CD4+CD25+调节性T细胞凋亡和干扰素γ (IFN-γ)分泌的影响。方法:对刚地弓形虫RH株和TgCtwh3株进行esa检测。取C57BL/6小鼠脾脏单个核细胞,随机分为RH ESA组(2×106细胞/孔,添加10 μg/ml RH ESA)、TgCtwh3 ESA组(2×106细胞/孔,添加10 μg/ml TgCtwh3 ESA)和对照组(2×106细胞/孔,添加10 μg/ml卵清蛋白)。流式细胞术检测CD4+CD25+调节性T细胞在治疗48 h和72 h后的早期凋亡情况,ELISA法检测治疗72 h后上清中IFN-γ的水平。另一个实验中,3组脾单核细胞分别加入10 μg/ml抗IFN-γ抗体,流式细胞术检测CD4+CD25+调节性T细胞早期凋亡情况。同时,将IFN-γ敲除小鼠和野生型C57BL/6小鼠脾单核细胞分为上述3组,流式细胞术检测治疗72 h后CD4+CD25+调节性T细胞早期凋亡情况。结果:RH ESA和TgCtwh3 ESA浓度分别为0.54 mg/ml和2.14 mg/ml。流式细胞术检测结果显示,RH ESA组和TgCtwh3 ESA组治疗48 h后CD4+CD25+调节性T细胞早期凋亡率分别为(12.90±1.26)%和(9.71±1.04)% (P<0.05),均显著高于对照组(4.48±0.48)% (P<0.05)。结论:弓形虫RH ESA诱导CD4+CD25+调节性T细胞凋亡和IFN-γ分泌,且作用强于TgCtwh3 ESA。弓形虫esa诱导的IFN-γ通过介导调节性T细胞凋亡刺激急性弓形虫感染期间抗弓形虫免疫的产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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