首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Enhanced cytotoxicity of IFN-gamma-producing CD4+ cytotoxic T lymphocytes specific for T. gondii-infected human melanoma cells.
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Enhanced cytotoxicity of IFN-gamma-producing CD4+ cytotoxic T lymphocytes specific for T. gondii-infected human melanoma cells.

机译:对刚地弓形虫感染的人黑素瘤细胞具有特异性的产生IFN-γ的CD4 +细胞毒性T淋巴细胞的增强的细胞毒性。

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摘要

CD4+ lines specific for Toxoplasma gondii-infected human melanoma P36 cells were established from PBL of a patient with chronic toxoplasmosis. CD4+ CTL lines were obtained by weekly in vitro stimulation with T. gondii-infected P36 cells that shared HLA-DR4 molecules with the patient. The lytic activity of CD4+ CTL lines against T. gondii-infected P36 or T. gondii-infected autologous EBV-transformed B lymphoma (EBV-Ya) was inhibited by anti-HLA-DR mAb, whereas anti-HLA-A, B, C mAb failed to block the lytic activity. Thus, the cytotoxicity of CD4+ CTL lines against T. gondii-infected P36 was restricted by HLA-DR molecules. In response to Ag-specific stimulation, CD4+ CTL lines produced significant levels of IFN-gamma. Exogenously added IFN-gamma up-regulated the surface expression of MHC class II, but not of class I in T. gondii-infected P36 cells. In addition, the CTL activity against T. gondii-infected P36 cells was augmented when target cells were co-cultured with IFN-gamma. These data indicate that CD4+ CTL-mediated cytotoxicity against T. gondii-infected melanocytes is enhanced by the autocrine production of IFN-gamma. Further, CD4+ CTL may play a role in the manifestation of toxoplasmic retinochoroiditis by killing T. gondii-infected melanocytes.
机译:从弓形虫病患者的PBL建立了弓形虫感染的人黑素瘤P36细胞特异的CD4 +系。通过每周一次用弓形虫感染的P36细胞进行体外刺激获得CD4 + CTL细胞系,该细胞与患者共享HLA-DR4分子。抗HLA-DR mAb可抑制CD4 + CTL系对弓形虫感染的P36或弓形虫感染的自体EBV转化的B淋巴瘤(EBV-Ya)的裂解活性,而抗HLA-A,B, C mAb无法阻断裂解活性。因此,HLA-DR分子限制了CD4 + CTL系对弓形虫感染的P36的细胞毒性。响应于Ag特异性刺激,CD4 + CTL系产生显着水平的IFN-γ。在刚地弓形虫感染的P36细胞中,外源添加的IFN-γ上调了MHC II类的表面表达,但不上调I类的表面表达。另外,当靶细胞与IFN-γ共培养时,针对刚地弓形虫感染的P36细胞的CTL活性增强。这些数据表明,CD4 + CTL介导的针对弓形虫感染的黑素细胞的细胞毒性通过IFN-γ的自分泌产生而增强。此外,CD4 + CTL可能通过杀死弓形虫感染的黑素细胞而在弓形体脉络膜脉络膜炎的表现中发挥作用。

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