O Dillman Robert
Chief Medical Officer, AIVITA Biomedical, Inc. Irvine, CA 92612, USA.
Clinical Professor Medicine, University of California Irvine, Irvine, CA 92697, USA.
Melanoma Manag. 2020 Jul 29;7(3):MMT49. doi: 10.2217/mmt-2020-0011.
GM-CSF drives the differentiation of granulocytes and monocyte/macrophages from hematopoietic stem cell progenitors. It is required for differentiating monocytes into dendritic cells (DC). Although approved for recovery of granulocytes/monocytes in patients receiving chemotherapy, G-CSF is preferred. Enthusiasm for GM-CSF monotherapy as a melanoma treatment was dampened by two large randomized trials. Although GM-CSF has been injected into tumors for many years, the efficacy of this has not been tested. There is a strong rationale for GM-CSF as a vaccine adjuvant, but it appears of benefit only for strategies that directly involve DCs, such as intratumor talimogene laherparepvec and vaccines in which DCs are loaded with antigen and injected admixed with GM-CSF.
粒细胞-巨噬细胞集落刺激因子(GM-CSF)驱动造血干细胞祖细胞分化为粒细胞和单核细胞/巨噬细胞。它是将单核细胞分化为树突状细胞(DC)所必需的。尽管GM-CSF被批准用于接受化疗患者的粒细胞/单核细胞恢复,但粒细胞集落刺激因子(G-CSF)更受青睐。两项大型随机试验减弱了人们对GM-CSF单药治疗黑色素瘤的热情。尽管GM-CSF已被注入肿瘤多年,但其疗效尚未得到检验。GM-CSF作为疫苗佐剂有充分的理论依据,但它似乎仅对直接涉及DC的策略有益,例如瘤内注射塔利莫基因拉赫帕里韦克以及将DC负载抗原并与GM-CSF混合注射的疫苗。