首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Granulocyte-macrophage colony-stimulating factor (GM-CSF) counteracts the inhibiting effect of monocytes on natural killer (NK) cells.
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Granulocyte-macrophage colony-stimulating factor (GM-CSF) counteracts the inhibiting effect of monocytes on natural killer (NK) cells.

机译:粒细胞巨噬细胞集落刺激因子(GM-CSF)抵消了单核细胞对自然杀伤(NK)细胞的抑制作用。

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摘要

GM-CSF is known to accelerate haematopoietic recovery following allogeneic bone marrow transplantation (BMT). In addition, it may restore and enhance both granulocyte and monocyte functions. Stimulation of monocyte functions may induce a direct or an indirect anti-leukaemic activity due to an increase of cellular cytotoxicity and production of cytokines which may result in a reduction of the relapse rate after BMT. NK cells may play a crucial role in this activity. Therefore we studied the influence of monocytes on NK activity in combination with GM-CSF. Lymphocytes and monocytes were isolated from buffy coats of healthy individuals by counterflow centrifugation elutriation (CCE). NK activity was exerted by CD3-CD56+ cell populations and could be enhanced by IL-2 incubation overnight. Incubation of CD3-CD56+ cells with GM-CSF in the presence or absence of IL-2 hardly influenced NK activity of the lymphocyte population. Low amounts of monocytes enhanced NK activity. NK activity in lymphocyte population in the presence of equivalent numbers of monocytes with or without IL-2 was strongly decreased irrespective of the effector:target ratio (ETR). This appeared not to result from sterical hindrance effects of the present number of cells. However, addition of GM-CSF abrogated the inhibition of NK activity by monocytes in the presence of IL-2. In monocyte fractions neither IL-2 nor GM-CSF yielded NK activity. Our findings indicate that GM-CSF can affect NK activity by counteracting the suppressing effects of monocytes, and hence may improve the outcome after BMT.
机译:已知GM-CSF可促进同种异体骨髓移植(BMT)后的造血恢复。另外,它可以恢复和增强粒细胞和单核细胞的功能。单核细胞功能的刺激可能由于细胞毒性的增加和细胞因子的产生而诱导直接或间接的抗白血病活性,这可能导致BMT后复发率降低。 NK细胞可能在此活动中起关键作用。因此,我们结合GM-CSF研究了单核细胞对NK活性的影响。通过逆流离心淘析(CCE)从健康个体的血沉棕黄层中分离出淋巴细胞和单核细胞。 NK活性由CD3-CD56 +细胞群体发挥,并可以通过IL-2过夜孵育而增强。在存在或不存在IL-2的情况下,使用GM-CSF孵育CD3-CD56 +细胞几乎不会影响淋巴细胞的NK活性。少量单核细胞可增强NK活性。无论是否有效应子:靶标比(ETR),在有相等数量的单核细胞存在或不存在IL-2的情况下,淋巴细胞数量中的NK活性都大大降低。这似乎不是由当前细胞数目的空间位阻效应引起的。然而,在IL-2存在下,添加GM-CSF消除了单核细胞对NK活性的抑制。在单核细胞级分中,IL-2和GM-CSF都不产生NK活性。我们的发现表明,GM-CSF可以通过抵消单核细胞的抑制作用来影响NK活性,因此可以改善BMT后的结局。

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