Virus-specific peptide dependent NK cell cytotoxicity.

Lan Tong, Mario Assenmacher, Kurt S Zänker, Peter Jähn
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引用次数: 8

Abstract

NK cells do not express recombination-dependent antigen-specific receptors and are traditionally defined as cells of the innate immune response. The activation of NK cells was believed to be controlled by the net balance of signals from a multitude of activating and inhibitory receptors irrespectively of antigen specificity. However, murine antigen-specific memory NK cells in liver have been described to mediate hapten or viral specific recall response and are capable of infiltrating to the site of infection. The mechanisms by which NK cells recognize target cells in an antigen-specific manner are largely unclear. Using a novel multiplex killing assay, we screened the NK cell (human) cytotoxic activity of 35 different donors against different virus peptide pools loaded autologous B cells. We have found that human NK cells from some CMV and EBV positive donors can recognize peptide loaded autologous B cells as targets and perform antigen-specific cytotoxic killing. This may provide evidence that NK cells are able to scan the peptide repertoire on the target cell surface and virus-derived peptides may influence the NK cell activation-inhibition balance.

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病毒特异性肽依赖性NK细胞的细胞毒性。
NK细胞不表达重组依赖抗原特异性受体,传统上被定义为先天性免疫应答细胞。NK细胞的激活被认为是由来自多种激活和抑制受体的信号的净平衡控制的,而与抗原特异性无关。然而,小鼠肝脏中的抗原特异性记忆NK细胞已被描述为介导半抗原或病毒特异性回忆反应,并且能够浸润到感染部位。NK细胞以抗原特异性方式识别靶细胞的机制在很大程度上尚不清楚。使用一种新的多重杀伤实验,我们筛选了35种不同供体的NK细胞(人)对不同病毒肽库负载的自体B细胞的细胞毒活性。我们发现来自某些CMV和EBV阳性供体的人类NK细胞可以识别装载肽的自体B细胞作为靶标,并进行抗原特异性细胞毒杀伤。这可能证明NK细胞能够扫描靶细胞表面的肽库,病毒衍生的肽可能影响NK细胞的激活-抑制平衡。
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