Ge Ke, Qiu Xiao-yan, Wang Li-juan, Chen Hui, Zhang Lu-yan, Qiu Jing-fan, Wang Yong
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2016 Jun;34(3):183-8.
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.
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.
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.
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.
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细胞凋亡及干扰素-γ(IFN-γ)分泌的影响。
制备刚地弓形虫RH株和TgCtwh3株的ESAs。从C57BL/6小鼠分离脾单个核细胞,随机分为RH ESA组(2×106个细胞/孔,加入10μg/ml RH ESA)、TgCtwh3 ESA组(2×106个细胞/孔,加入10μg/ml TgCtwh3 ESA)和对照组(2×106个细胞/孔,加入10μg/ml卵清蛋白)。处理48小时和72小时后,采用流式细胞术检测CD4+CD25+调节性T细胞的早期凋亡情况。处理72小时后,采用ELISA法测定上清液中IFN-γ水平。在另一实验中,3组脾单个核细胞加入10μg/ml抗IFN-γ抗体作用72小时,采用流式细胞术检测CD4+CD25+调节性T细胞的早期凋亡情况。同时,将IFN-γ基因敲除和野生型C57BL/6小鼠的脾单个核细胞也分为上述3组,处理72小时后采用流式细胞术检测CD4+CD25+调节性T细胞的早期凋亡情况。
RH ESA和TgCtwh3 ESA的浓度分别为0.54mg/ml和2.14mg/ml。流式细胞术显示,处理48小时后,RH ESA组和TgCtwh3 ESA组CD4+CD25+调节性T细胞的早期凋亡率分别为(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<0.01)。处理72小时后,RH ESA组CD4+CD25+调节性T细胞的早期凋亡率为(15.21±1.11)%,显著高于TgCtwh3 ESA组[(11.02±0.92)%](P<0.05)和对照组[(10.10±1.49)%](P<0.01)。ELISA显示,处理72小时后,RH ESA组和TgCtwh3 ESA组的干扰素-γ水平分别为(4764.0±118.7)pg/ml和(3629.0±33.6)pg/ml(P<0.01),均显著高于对照组[(679.4±30.6)pg/ml](P<0.01)。流式细胞术显示,加入抗IFN-γ抗体的RH ESA组CD4+CD25+调节性T细胞的早期凋亡率[(10.44±1.44)%]低于未加抗体组[(14.96±0.83)%](P<0.05)。但TgCtwh3 ESA组未观察到这种差异。此外,IFN-γ基因敲除小鼠的RH ESA诱导的调节性T细胞凋亡率[(10.64±0.55)%]显著低于野生型小鼠[(15.21±1.11)%](P<0.01)。但TgCtwh3 ESA处理未发现这种差异。
刚地弓形虫RH ESA诱导CD4+CD25+调节性T细胞凋亡及IFN-γ分泌,且这些作用强于TgCtwh3 ESA。刚地弓形虫ESA诱导的IFN-γ通过介导调节性T细胞凋亡,在急性弓形虫感染期间刺激抗弓形虫免疫的产生。