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首页> 外文期刊>Mechanisms of Ageing and Development >Age-associated decline in IL-2 and IL-12 induction of LAK cell activity of human PBMC samples.
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Age-associated decline in IL-2 and IL-12 induction of LAK cell activity of human PBMC samples.

机译:人PBMC样品的IL-2和IL-12诱导的LAK细胞活性的年龄相关下降。

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Previously we reported that young and elderly natural killer (NK) cell activity against the standard NK sensitive K562 cell line can be augmented to the same degree by IL-2 and IFN-alpha. We have extended these studies to include IL-12. Similar to IL-2 and IFN-alpha, IL-12 can enhance NK cytotoxicity to the same degree in both young and elderly samples over a wide range of doses and incubation times when K562 cells are used as targets. However, in contrast to our findings with the NK system, we have observed that induction of lymphokine activated killer (LAK) cell activity, as defined by the ability of peripheral blood mononuclear cells (PBMC) samples to lyse the normally NK resistant Daudi cell line, was significantly decreased in the elderly samples compared to young samples. Comparable age-associated differences were observed in LAK activity after induction with IL-2, IL-12, and IFN-alpha at varying doses and incubation times. We hypothesize an age-associated deficiency either in the mechanism of LAK induction or in target cell recognition.
机译:以前我们曾报道过,IL-2和IFN-α可以将针对标准NK敏感K562细胞系的年轻和老年人自然杀伤(NK)细胞活性提高到相同程度。我们将这些研究扩展到包括IL-12。与IL-2和IFN-α相似,当将K562细胞用作靶标时,IL-12可以在很宽的剂量和孵育时间范围内,在年轻人和老年人样品中以相同的程度增强NK细胞毒性。但是,与我们在NK系统中的发现相反,我们已经观察到淋巴因子激活的杀伤(LAK)细胞活性的诱导,这由外周血单核细胞(PBMC)样品裂解正常的NK抗性Daudi细胞系的能力来定义与年轻样本相比,老年人样本中的,明显降低。在以不同的剂量和孵育时间用IL-2,IL-12和IFN-α诱导后,LAK活性观察到了与年龄相关的可比差异。我们假设LAK诱导机制或靶细胞识别中年龄相关的缺陷。

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