Ke Ge, Xiao-yan Qiu, Li-juan Wang, Hui Chen, Lu-yan Zhang, Jing-fan Qiu, Yong Wang
{"title":"[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]。","authors":"Ke Ge, Xiao-yan Qiu, Li-juan Wang, Hui Chen, Lu-yan Zhang, Jing-fan Qiu, Yong Wang","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":23981,"journal":{"name":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","volume":"34 3","pages":"183-8"},"PeriodicalIF":0.0000,"publicationDate":"2016-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Interferon-γ Induced by Toxoplasma gondii Excreted/Secreted Antigens Promotes Apoptosis of CD4+CD25+ Regulatory T Cells].\",\"authors\":\"Ke Ge, Xiao-yan Qiu, Li-juan Wang, Hui Chen, Lu-yan Zhang, Jing-fan Qiu, Yong Wang\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>\",\"PeriodicalId\":23981,\"journal\":{\"name\":\"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases\",\"volume\":\"34 3\",\"pages\":\"183-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhongguo ji sheng chong xue yu ji sheng chong bing za zhi = Chinese journal of parasitology & parasitic diseases","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Interferon-γ Induced by Toxoplasma gondii Excreted/Secreted Antigens Promotes Apoptosis of CD4+CD25+ Regulatory T Cells].
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.