In vivo administration of recombinant macrophage colony-stimulating factor induces macrophage-mediated antibody-dependent cytotoxicity of tumor cells.

M G Sanda, E Bolton, J J Mulé, S A Rosenberg
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引用次数: 24

Abstract

Macrophage colony-stimulating factor (M-CSF) has been previously shown to facilitate the in vitro survival and differentiation of mononuclear phagocytes. We assessed whether M-CSF administration in vivo could induce macrophages capable of killing tumor via an antibody-dependent mechanism. C57BL/6 mice were given intraperitoneal M-CSF, and peritoneal macrophages were assayed for their ability to kill fluorochrome-labeled R1.1 thymoma cells in vitro in the presence or absence of target-specific antibody. Two-color flow cytometry was used in measuring tumor ingestion by macrophages; macrophages from M-CSF-treated mice eliminated greater than 90% of R1.1 thymoma target within 24 hours, while macrophages from saline-treated controls were ineffective. R1.1 tumor elimination by macrophages depended on the presence of target-specific antibody. These are the first studies that demonstrate the in vivo induction, by M-CSF, of macrophages directly capable of ingesting antibody-conjugated tumor cells.

体内给药重组巨噬细胞集落刺激因子可诱导巨噬细胞介导的抗体依赖性肿瘤细胞毒性。
巨噬细胞集落刺激因子(M-CSF)先前已被证明可促进单核吞噬细胞的体外存活和分化。我们评估了体内给药M-CSF是否能诱导巨噬细胞通过抗体依赖机制杀死肿瘤。给C57BL/6小鼠腹腔注射M-CSF,检测腹腔巨噬细胞在存在或不存在靶特异性抗体的情况下体外杀死荧光色标记的R1.1胸腺瘤细胞的能力。采用双色流式细胞术检测巨噬细胞对肿瘤的吞噬;m - csf处理小鼠的巨噬细胞在24小时内消除了90%以上的R1.1胸腺瘤靶点,而盐水处理对照组的巨噬细胞则无效。R1.1巨噬细胞消除肿瘤依赖于靶标特异性抗体的存在。这些研究首次证明了M-CSF在体内诱导巨噬细胞直接摄取抗体结合的肿瘤细胞。
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