Frohn Christoph, Höppner Maike, Schlenke Peter, Kirchner Holger, Koritke Petra, Luhm Jürgen
Institute of Immunology and Transfusion Medicine, University of Lübeck, Lübeck, Germany.
Br J Haematol. 2002 Dec;119(3):660-4. doi: 10.1046/j.1365-2141.2002.03879.x.
Natural killer (NK) cells are assumed to contribute to a graft-versus-leukaemia effect. In vitro experiments have shown that many leukaemic cells are NK-cell sensitive. Nevertheless, no data concerning the influence of purified NK cells on malignant myeloma (MM) cells exist. We co-incubated NK cells with three different MM cell lines and fresh bone marrow samples of nine MM patients. The proportion of vital MM cells was determined before and after co-cultivation by a flow-cytometry-based assay. All MM cells tested, with the exception of one cell line (NCI H929), were susceptible to a NK-cell attack even without exogenous interleukin 2 (IL-2). The mean killing of the native MM samples was 23.1 +/- 5.4% and 34.5 +/- 6.5% at 10:1 and 20:1 effector:target ratio respectively, This corresponded to about 2/3 of those values obtained with the highly sensitive line K562. In contrast, CD34-positive haematopoietic stem cells as well as peripheral mononuclear cells were completely resistant under similar experimental conditions (1.3% killing). To elucidate the underlying triggering mechanisms, we measured human leucocyte antigen (HLA)-class I expression of the MM cells. No evidence for HLA loss, which could have explained the NK-cell recognition if it occurred, was demonstrated. These findings may contribute to the understanding of in vivo NK-cell activation and encourage clinical applications of NK cells for MM patients.
自然杀伤(NK)细胞被认为有助于产生移植物抗白血病效应。体外实验表明,许多白血病细胞对NK细胞敏感。然而,目前尚无关于纯化的NK细胞对恶性骨髓瘤(MM)细胞影响的数据。我们将NK细胞与三种不同的MM细胞系以及9例MM患者的新鲜骨髓样本共同培养。通过基于流式细胞术的检测方法,在共培养前后测定存活MM细胞的比例。除一种细胞系(NCI H929)外,所有测试的MM细胞即使在没有外源性白细胞介素2(IL-2)的情况下也易受NK细胞攻击。在效应细胞与靶细胞比例为10:1和20:1时,天然MM样本的平均杀伤率分别为23.1±5.4%和34.5±6.5%,这大约相当于用高敏感性细胞系K562所获得值的2/3。相比之下,在类似实验条件下,CD34阳性造血干细胞以及外周单个核细胞完全耐药(杀伤率为1.3%)。为阐明潜在的触发机制,我们检测了MM细胞的人类白细胞抗原(HLA)-I类表达。未发现HLA缺失的证据,若HLA缺失发生,本可解释NK细胞的识别情况。这些发现可能有助于理解体内NK细胞的激活,并鼓励将NK细胞应用于MM患者的临床治疗。