首页> 外文期刊>Vaccine >Simultaneous cognate epitope recognition by bovine CD4 and CD8 T cells is essential for primary expansion of antigen-specific cytotoxic T-cells following ex vivo stimulation with a candidate Mycobacterium avium subsp. paratuberculosis peptide vaccine
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Simultaneous cognate epitope recognition by bovine CD4 and CD8 T cells is essential for primary expansion of antigen-specific cytotoxic T-cells following ex vivo stimulation with a candidate Mycobacterium avium subsp. paratuberculosis peptide vaccine

机译:牛CD4和CD8 T细胞的同时同学表位识别对于抗原特异性细胞毒性T细胞的原发性膨胀是必不可少的,所述抗原特异性细胞毒性T细胞与候选分枝杆菌患者的抗钙刺激后抗原特异性细胞毒性T细胞。 paratuberculosis肽疫苗

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Studies in cattle show CD8 cytotoxic T cells (CTL), with the ability to kill intracellular bacteria, develop following stimulation of monocyte-depleted peripheral blood mononuclear cells (mdPBMC) with antigen presenting cells (APC, i.e. conventional dendritic cells [cDC] and monocyte-derived DC [MoDC]) pulsed with MMP, a membrane protein from Mycobacterium avium subsp. paratuberculosis (Map) encoded by MAP2121c. CTL activity was diminished if CD4 T cells were depleted from mdPBMC before antigen (Ag) presentation by APC, suggesting simultaneous cognate recognition of MMP epitopes presented by MHC I and MHC II molecules to CD4 and CD8 T cells is essential for development of CTL activity. To explore this possibility, studies were conducted with mdPBMC cultures in the presence of monoclonal antibodies (mAbs) specific for MHC class I and MHC class II molecules. The CTL response of mdPBMC to MMP-pulsed APC was completely blocked in the presence of mAbs to both MHC I and II molecules and also blocked in the presence of mAbs to either MHC I or MHC II alone. The results demonstrate simultaneous cognate recognition of Ag by CD4 and CD8 T cells is essential for delivery of CD4 T cell help to CD8 T cells to elicit development of CTL. (C) 2019 Elsevier Ltd. All rights reserved.
机译:在牛中的研究表明CD8细胞毒性T细胞(CTL),具有杀细胞内细菌,与抗原呈递细胞(APC,即常规树突状细胞[CDC]和单核细胞培养的单核细胞耗尽外周血单核细胞的刺激后(mdPBMC)的能力脉冲与MMP,从鸟分枝杆菌亚种的膜蛋白衍生的DC [的MoDC])。副结核病(MAP)通过编码MAP2121c。如果CD4 + T细胞从mdPBMC之前由APC抗原(Ag)的介绍耗尽,表明MMP的同时同源识别的表位由MHC I和MHC II分子CD4和CD8 T细胞呈现为CTL活性的发展至关重要CTL活性降低。为了探究这种可能性,研究使用mdPBMC培养物在单克隆抗体(mAbs)的特异性的存在下,MHC I类和MHC II类分子进行。 mdPBMC对MMP-脉冲APC的CTL应答被完全阻断mAb的存在既MHC I和II类分子,并且还阻断mAb的存在要么MHC I或MHC II单独。结果表明银的同时同源识别由CD4和CD8 T细胞是交付的CD4 T细胞帮助CD8 T细胞的CTL引导学生发展至关重要。 (c)2019 Elsevier Ltd.保留所有权利。

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