AML原细胞刺激诱导细胞毒性淋巴细胞亚群抗白血病。

E Lotzová, C A Savary
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引用次数: 3

摘要

尽管白细胞介素-2 (IL-2)活化淋巴细胞在急性髓性白血病(AML)免疫治疗中的应用具有治疗意义,但AML原细胞对淋巴细胞溶解的高耐药性可能是这种治疗的障碍。然而,我们的数据显示,白血病的耐药性可以通过淋巴细胞与IL-2和AML原细胞共同培养来克服。这种方法不仅诱导白血病导向的细胞毒性细胞,而且还促进它们的生长。此外,在AML/IL-2培养中诱导具有白血病溶解活性的多种细胞毒性淋巴细胞群。这些细胞包括自然杀伤细胞(NK)和T细胞亚群,它们具有主要组织相容性复合体(MHC)限制性和MHC非限制性细胞毒性功能。因此,该方案有利于对白血病的细胞免疫反应的一般刺激,可能会增强淋巴细胞治疗的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of cytotoxic lymphocyte subsets against leukemia by stimulation with AML blasts.

Although the application of interleukin-2 (IL-2) activated lymphocytes in immunotherapy of acute myelogenous leukemia (AML) is of therapeutic interest, the high resistance of AML blasts to lymphocyte lysis may represent an obstacle to this type of therapy. However, our data shows that the leukemia resistance can be conquered by concomitant culture of lymphocytes with IL-2 and AML blasts. This approach induces not only leukemia-directed cytotoxic cells, but also promotes their growth. Additionally, multiple cytotoxic lymphocyte populations with leukemia lytic activity are induced in AML/IL-2 cultures. These include natural killer (NK) cells and subsets of T cells with both the major histocompatibility complex (MHC)-restricted and MHC-nonrestricted cytotoxic function. Thus, this protocol, which is conducive to general stimulation of cellular immune responses against leukemia, may enhance the benefits of lymphocyte therapy.

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