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一种靶向粒细胞巨噬细胞集落刺激因子受体的重组融合毒素。

A recombinant fusion toxin targeted to the granulocyte-macrophage colony-stimulating factor receptor.

作者信息

Bendel A E, Shao Y, Davies S M, Warman B, Yang C H, Waddick K G, Uckun F M, Perentesis J P

机构信息

Biotherapy Institute, University of Minnesota Academic Health Center, Minneapolis, USA.

出版信息

Leuk Lymphoma. 1997 Apr;25(3-4):257-70. doi: 10.3109/10428199709114165.

Abstract

Human granulocyte-macrophage colony stimulating factor (GMCSF) and its high affinity receptor function to regulate the proliferation and differentiation of myeloid lineage hematopoietic cells, and may participate in the pathogenesis of many malignant myeloid diseases. We have used genetic engineering based on the elucidated molecular structures of human granulocyte-macrophage colony-stimulating factor and diphtheria toxin (DT) to produce a recombinant fusion toxin, DTctGMCSF, that targets diphtheria toxin to high affinity GMCSF receptors expressed on the surface of blast cells from a large fraction of patients with acute myeloid leukemia (AML). DTctGMCSF was specifically immunoreactive with antidiphtheria toxin and anti-GMCSF antiseras, and exhibited the characteristic catalytic activity of diphtheria toxin, catalyzing the in vitro ADP-ribosylation of purified elongation factor 2. The cytotoxic effects of DTctGMCSF were examined using the 3-(4,5-dimethylthiazol-2-yl)-2,5-tetrazolium (MTT) bromide assay of cell viability and in vivo assays of protein synthesis inhibition. DTctGMCSF were specifically cytotoxic to human leukemia cell lines bearing high affinity receptors for human GMCSF with IC50 of 10(-9) to 10(-11) M. It was not toxic to mammalian hematopoietic cell lines lacking human GMCSF (hGMCSF) receptors. In receptor positive cells, cytotoxicity can be specifically blocked by a large excess of hGMCSF, confirming that its cytotoxicity is mediated through the hGMCSF receptor. THough DTctGMCSF inhibited granulocyte-macrophage colony formation by committed myeloid progenitor cells (CFU-GM), it did not significantly affect erythroid burst formation by committed erythroid progenitor cells (BFU-E), or mixed granulocyte-erythroid-macrophage-megakaryocyte colony formation by pluripotent multilineage progenitor cells (CFU-GEMM). DTctGMCSF holds promise for the treatment of myeloid lineage malignancies, and is a useful reagent to study hematopoiesis.

摘要

人粒细胞巨噬细胞集落刺激因子(GMCSF)及其高亲和力受体可调节髓系造血细胞的增殖和分化,并可能参与多种恶性髓系疾病的发病机制。我们基于已阐明的人粒细胞巨噬细胞集落刺激因子和白喉毒素(DT)的分子结构,利用基因工程技术制备了一种重组融合毒素DTctGMCSF,该毒素可将白喉毒素靶向至大部分急性髓系白血病(AML)患者原始细胞表面表达的高亲和力GMCSF受体。DTctGMCSF与抗白喉毒素和抗GMCSF抗血清具有特异性免疫反应,并表现出白喉毒素的特征性催化活性,能催化纯化的延伸因子2的体外ADP核糖基化。使用3-(4,5-二甲基噻唑-2-基)-2,5-四氮唑溴盐(MTT)细胞活力测定法和体内蛋白质合成抑制测定法检测了DTctGMCSF的细胞毒性作用。DTctGMCSF对表达人GMCSF高亲和力受体的人白血病细胞系具有特异性细胞毒性,IC50为10^(-9)至10^(-11) M。它对缺乏人GMCSF(hGMCSF)受体的哺乳动物造血细胞系无毒。在受体阳性细胞中,大量过量的hGMCSF可特异性阻断细胞毒性,证实其细胞毒性是通过hGMCSF受体介导的。尽管DTctGMCSF抑制了定向髓系祖细胞(CFU-GM)形成粒细胞巨噬细胞集落,但它对定向红系祖细胞(BFU-E)形成红系爆式集落或多能多系祖细胞(CFU-GEMM)形成混合粒细胞-红系-巨噬细胞-巨核细胞集落没有显著影响。DTctGMCSF有望用于治疗髓系恶性肿瘤,是研究造血作用的有用试剂。

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