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PIXY321(粒细胞-巨噬细胞集落刺激因子/白细胞介素-3融合蛋白):生物学特性与早期临床开发

PIXY321 (GM-CSF/IL-3 fusion protein): biology and early clinical development.

作者信息

Vadhan-Raj S

机构信息

Department of Clinical Immunology and Biological Therapy, University of Texas M. D. Anderson Cancer Center, Houston 77030.

出版信息

Stem Cells. 1994 May;12(3):253-61. doi: 10.1002/stem.5530120302.

Abstract

Granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-3 (IL-3) are functionally related hematopoietins with overlapping but distinct hematopoietic effects. GM-CSF supports more myeloid progenitor cells, whereas IL-3 promotes more erythroid, megakaryocytic and multipotential progenitor cells. Their complementary in vivo biological effects and cross competition for receptor binding prompted the development of PIXY321, a synthetic hybrid protein of GM-CSF and IL-3. PIXY321 binds to cell lines expressing specific receptors for either ligand, and it exhibits enhanced biological activity in human hematopoietic progenitor cell assays. In preclinical studies, PIXY321 has been shown to accelerate both neutrophil and platelet recovery in rhesus monkeys subjected to sublethal irradiation. Based on these preclinical observations, clinical trials have been initiated examining the therapeutic potential of this agent in ameliorating treatment- or disease-related hematopoietic suppression. The early results indicate that PIXY321 can stimulate multilineage hematopoiesis in vivo and enhance neutrophil and platelet recovery following chemotherapy and bone marrow transplantation (BMT). These results suggest that PIXY321 elicits the biological effects of both its component cytokines and represents a novel means of delivering two independent but interactive cytokines in combination.

摘要

粒细胞-巨噬细胞集落刺激因子(GM-CSF)和白细胞介素-3(IL-3)是功能相关的造血因子,具有重叠但不同的造血作用。GM-CSF支持更多的髓系祖细胞,而IL-3促进更多的红系、巨核系和多能祖细胞。它们在体内的互补生物学效应以及对受体结合的交叉竞争促使了PIXY321的开发,PIXY321是GM-CSF和IL-3的合成杂交蛋白。PIXY321与表达任一配体特异性受体的细胞系结合,并且在人类造血祖细胞试验中表现出增强的生物学活性。在临床前研究中,已证明PIXY321可加速接受亚致死剂量照射的恒河猴的中性粒细胞和血小板恢复。基于这些临床前观察结果,已启动临床试验以研究该药物在改善治疗或疾病相关造血抑制方面的治疗潜力。早期结果表明,PIXY321可在体内刺激多谱系造血,并增强化疗和骨髓移植(BMT)后中性粒细胞和血小板的恢复。这些结果表明,PIXY321引发了其两种组成细胞因子的生物学效应,并代表了一种将两种独立但相互作用的细胞因子联合递送的新方法。

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