首页> 外文期刊>Human Immunology: Official Journal of the American Society for Histocompatibility and Immunogenetics >Up-regulation of DNAM-1 and NKp30, associated with improvement of NK cells activation after long-term culture of mononuclear cells from patients with ovarian neoplasia
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Up-regulation of DNAM-1 and NKp30, associated with improvement of NK cells activation after long-term culture of mononuclear cells from patients with ovarian neoplasia

机译:长期培养卵巢肿瘤患者单核细胞后,DNAM-1和NKp30的上调与NK细胞活化的改善有关

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摘要

This study aimed at evaluating the functional activation and activating receptors expression on resting, short- and long-term NK and NK-like T cells from blood of ovarian neoplasia patients. Blood from patients with adnexal benign alterations (n=10) and ovarian cancer (grade I-IV n=14) were collected after signed consent. Effector cells activation was evaluated by the expression of the CD107a molecule. Short-term culture was conducted overnight with IL-2 and long-term culture for 21days, by a method designed to expand CD56+ lymphocytes. Short-term culture significantly increased NK cells activation compared to resting NK cells (p0.05), however, the long-term procedure supported an even higher increase (p0.001). Resting NK-like T cells showed poor activation, which was not altered by the culture procedures. The long-term culture effectively increased the expression of the activating receptors on NK and NK-like T cells, either by increasing the number of cells expressing a given receptor and/or by up-regulating their expression intensity. As a conclusion, the long-term culture system employed, resulted in a high number of functional NK cells. The culture system was particularly efficient on the up-regulation of NKp30 and DNAM-1 receptors on NK cells.
机译:这项研究旨在评估卵巢肿瘤患者血液中静止,短期和长期的NK和NK样T细胞的功能性激活和激活受体表达。签署同意书后,从附件良性改变(n = 10)和卵巢癌(I-IV级n = 14)患者中收集血液。通过CD107a分子的表达评估效应细胞的活化。通过设计用于扩增CD56 +淋巴细胞的方法,用IL-2进行短期培养过夜,并进行21天长期培养。与静息NK细胞相比,短期培养显着增加了NK细胞的活化(p <0.05),但是,长期操作支持更高的增加(p <0.001)。静止的NK样T细胞显示出较差的活化,这没有被培养程序改变。长期培养可以通过增加表达给定受体的细胞数量和/或通过上调其表达强度来有效地增加激活受体在NK和NK样T细胞上的表达。结论是,采用的长期培养系统导致大量功能性NK细胞。该培养系统在NK细胞上NKp30和DNAM-1受体的上调方面特别有效。

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