体外研究脂质体白细胞介素-2活性。

Molecular biotherapy Pub Date : 1992-03-01
M Adibzadeh, H G Weder, A Rehbein, U Schwuléra, J Obermeier, G Pawelec
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引用次数: 0

摘要

在短期和长期t细胞克隆和繁殖系统中,以及在实验中测试淋巴因子激活杀伤细胞(LAK)的诱导作用,对包装在卵磷脂脂质体中的高纯度天然人白细胞介素-2 (IL-2)进行了临床前体外评估。脂质体IL-2 (lip-IL-2)在辅助T细胞和细胞毒性同种异体反应性T细胞的克隆和培养中基本上与游离的天然或重组IL-2一样具有活性。然而,在诱导来自正常供体的LAK细胞方面,lip-IL-2被发现明显低于游离天然或重组IL-2。然而,唇IL-2能够维持游离IL-2预先激活的群体的LAK细胞毒性。这些结果表明,lip-IL-2可以以与游离IL-2相同的方式与活化的T细胞和LAK细胞相互作用,但在激活LAK细胞前体时效率要低得多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activity of liposomal interleukin-2 in vitro.

Preclinical in vitro assessment of highly purified natural human interleukin-2 (IL-2) packed in egg lecithin liposomes was performed in short- and long-term T-cell cloning and propagation systems, and in experiments testing induction of lymphokine-activated killer (LAK) cells. Liposomal IL-2 (lip-IL-2) was essentially as active as free natural or recombinant IL-2 for cloning and culture of both helper and cytotoxic alloreactive T cells. However, lip-IL-2 was found to be markedly inferior to free natural or recombinant IL-2 for the induction of LAK cells from normal donors. Nevertheless, lip-IL-2 was able to maintain LAK cytotoxicity of populations preactivated with free IL-2. These results suggest that lip-IL-2 can interact with activated T cells and LAK cells in the same way as free IL-2, but that it is much less efficient at activating LAK-cell precursors.

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