首页> 美国卫生研究院文献>other >Influence of In Vitro IL-2 or IL-15 Alone or in Combination with Hsp 70 Derived 14-Mer Peptide (TKD) on the Expression of NK Cell Activatory and Inhibitory Receptors on Peripheral Blood T Cells B Cells and NKT Cells
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Influence of In Vitro IL-2 or IL-15 Alone or in Combination with Hsp 70 Derived 14-Mer Peptide (TKD) on the Expression of NK Cell Activatory and Inhibitory Receptors on Peripheral Blood T Cells B Cells and NKT Cells

机译:单独或与Hsp 70衍生的14-mer肽(TKD)联合使用的体外IL-2或IL-15对外周血T细胞B细胞和NKT细胞上NK细胞活化和抑制受体表达的影响

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摘要

Previous studies from Multhoff and colleagues reported that plasma membrane Hsp70 acts as a tumour-specific recognition structure for activated NK cells, and that the incubation of NK cells with Hsp70 and/or a 14-mer peptide derived from the N-terminal sequence of Hsp70 (TKDNNLLGRFELSG, TKD, aa 450–463) plus a low dose of IL-2 triggers NK cell proliferation and migration, and their capacity to kill cancer cells expressing membrane Hsp70. Herein, we have used flow cytometry to determine the influence of in vitro stimulation of peripheral blood mononuclear cells from healthy individuals with IL-2 or IL-15, either alone or in combination with TKD peptide on the cell surface expression of CD94, NK cell activatory receptors (CD16, NK2D, NKG2C, NKp30, NKp44, NKp46, NKp80, KIR2DL4, DNAM-1 and LAMP1) and NK cell inhibitory receptors (NKG2A, KIR2DL2/L3, LIR1/ILT-2 and NKR-P1A) by CD3+CD56+ (NKT), CD3+CD4+, CD3+CD8+ and CD19+ populations. NKG2D, DNAM-1, LAMP1 and NKR-P1A expression was upregulated after the stimulation with IL-2 or IL-15 alone or in combination with TKD in NKT, CD8+ T cells and B cells. CD94 was upregulated in NKT and CD8+ T cells. Concurrently, an increase in a number of CD8+ T cells expressing LIR1/ILT-2 and CD4+ T cells positive for NKR-P1A was observed. The proportion of CD8+ T cells that expressed NKG2D was higher after IL-2/TKD treatment, when compared with IL-2 treatment alone. In comparison with IL-15 alone, IL-15/TKD treatment increased the proportion of NKT cells that were positive for CD94, LAMP1 and NKRP-1A. The more potent effect of IL-15/TKD on cell surface expression of NKG2D, LIR1/ILT-2 and NKRP-1A was observed in B cells compared with IL-15 alone. However, this increase was not of statistical significance. IL-2/TKD induced significant upregulation of LAMP1 in CD8+ T cells compared with IL-2 alone. Besides NK cells, other immunocompetent cells present within the fraction of peripheral blood mononuclear cells were influenced by the treatment with low-dose interleukins themselves or in combination with hsp70 derived (TKD) peptide.
机译:Multhoff及其同事的先前研究报道,质膜Hsp70充当激活的NK细胞的肿瘤特异性识别结构,并且将NK细胞与Hsp70和/或源自Hsp70 N端序列的14-mer肽一起孵育(TKDNNLLGRFELSG,TKD,aa 450-463)加上低剂量的IL-2会触发NK细胞增殖和迁移,并杀死表达Hsp70膜的癌细胞。在本文中,我们已经使用流式细胞术来确定体外用IL-2或IL-15单独或与TKD肽组合刺激健康个体的外周血单个核细胞对CD94,NK细胞表面表达的影响CD3 +激活受体(CD16,NK2D,NKG2C,NKp30,NKp44,NKp46,NKp80,KIR2DL4,DNAM-1和LAMP1)和NK细胞抑制受体(NKG2A,KIR2DL2 / L3,LIR1 / ILT-2和NKR-P1A) CD56 +(NKT),CD3 + CD4 +,CD3 + CD8 +和CD19 +种群。在NKT,CD8 + T细胞和B细胞中,单独用IL-2或IL-15或与TKD联合刺激后,NKG2D,DNAM-1,LAMP1和NKR-P1A的表达上调。 CD94在NKT和CD8 + T细胞中上调。同时,观察到表达LIR1 / ILT-2的CD8 + T细胞和NKR-P1A阳性的CD4 + T细胞数量增加。与单独的IL-2治疗相比,IL-2 / TKD治疗后表达NKG2D的CD8 + T细胞比例更高。与单独的IL-15相比,IL-15 / TKD处理可增加CD94,LAMP1和NKRP-1A阳性的NKT细胞比例。与单独的IL-15相比,在B细胞中观察到IL-15 / TKD对NKG2D,LIR1 / ILT-2和NKRP-1A细胞表面表达的更强效作用。但是,这种增加没有统计学意义。与单独的IL-2相比,IL-2 / TKD诱导CD8 + T细胞中LAMP1的显着上调。除NK细胞外,存在于外周血单核细胞部分中的其他免疫活性细胞也受到低剂量白介素自身或与hsp70衍生(TKD)肽联合治疗的影响。

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