Lymphoid Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Clinical Center, Bethesda, Maryland 20892-1374.
Cold Spring Harb Perspect Biol. 2018 Dec 3;10(12):a028472. doi: 10.1101/cshperspect.a028472.
Cytokines that control the immune response were shown to have efficacy in preclinical murine cancer models. Interferon (IFN)-α is approved for treatment of hairy cell leukemia, and interleukin (IL)-2 for the treatment of advanced melanoma and metastatic renal cancer. In addition, IL-12, IL-15, IL-21, and granulocyte macrophage colony-stimulating factor (GM-CSF) have been evaluated in clinical trials. However, the cytokines as monotherapy have not fulfilled their early promise because cytokines administered parenterally do not achieve sufficient concentrations in the tumor, are often associated with severe toxicities, and induce humoral or cellular checkpoints. To circumvent these impediments, cytokines are being investigated clinically in combination therapy with checkpoint inhibitors, anticancer monoclonal antibodies to increase the antibody-dependent cellular cytotoxicity (ADCC) of these antibodies, antibody cytokine fusion proteins, and anti-CD40 to facilitate tumor-specific immune responses.
控制免疫反应的细胞因子在临床前的小鼠癌症模型中显示出疗效。干扰素 (IFN)-α 已被批准用于治疗毛细胞白血病,白细胞介素 (IL)-2 用于治疗晚期黑色素瘤和转移性肾细胞癌。此外,IL-12、IL-15、IL-21 和粒细胞巨噬细胞集落刺激因子 (GM-CSF) 已在临床试验中进行了评估。然而,细胞因子作为单一疗法并没有实现其早期的承诺,因为细胞因子经肠胃外给药并不能在肿瘤中达到足够的浓度,常常与严重的毒性相关,并诱导体液或细胞检查点。为了克服这些障碍,细胞因子正在与检查点抑制剂联合治疗进行临床研究,以增加这些抗体的抗体依赖的细胞毒性 (ADCC),抗体细胞因子融合蛋白和抗 CD40,以促进肿瘤特异性免疫反应。