Vera-Aguilera Jesus, Perez-Torres Armando, Beltran Diego, Villanueva-Ramos Cynthia, Wachtel Mitchell, Moreno-Aguilera Eduardo, Vera-Aguilera Carlos, Ventolini Gary, Martínez-Zaguilán Raul, Sennoune Souad R
1 Division of Hematology, Mayo Clinic , Rochester, Minnesota.
2 Division of Oncology, Mayo Clinic , Rochester, Minnesota.
Cancer Biother Radiopharm. 2017 Mar;32(2):49-56. doi: 10.1089/cbr.2016.2123.
Recent successes in the development of new therapies for metastatic melanoma, such as mitogen-activated protein kinase pathway inhibitors, anticytotoxic T lymphocyte-associated antigen-4, and programmed cell death protein 1/programmed cell death ligand 1 (PD-L1) pathway-blocking antibodies, as well as combination strategies, all yielded promising results, changing the continually evolving landscape of therapeutic options for patients with melanoma. One promising new treatment modality is based on the use of immunomodulatory monoclonal antibodies that enhance the function of components of the antitumor immune response such as T cells or block immunologic checkpoints that restrain effective antitumor immunity. Program death-1 receptor and its ligand, PD-L1, is a major mechanism by which a tumor suppresses T cell-mediated antitumor immune responses. Studies in mice have shown that GK-1, an 18 amino acid peptide from Taenia crassiceps cisticerci, has the potential to be used as a primary or adjuvant component for the treatment of cancers by stimulating proinflammatory cytokines. The authors hypothesized that treatment with GK-1 in combination with anti-PD-L1 will increase survival in mice bearing melanoma tumors. C57BL/6 mice were injected with B16-F10-luc2 cells and separated into four groups: control, GK-1, anti-PD-L1, and GK-1/anti-PD-L1. The tumor sizes were measured and monitored using calipers and bioluminescence. The GK-1 peptide in combination with anti-PD-L1 showed significantly longer survival (34 days) compared with the other groups (23-27 days). This means an increase; survival increased 47.82% in the mice treated with GK-1+anti-PD-L1, 21.7% in mice treated with GK-1 alone, and 6.08% in those mice treated with anti-PD-L1 only. Blood samples were collected at days 0, 14, and at euthanization or end of the experiment and monitored for cytokines using mouse-specific V-PLEX Proinflammatory Panel. A decrease in TNF-α, IL-4, IL-5, IL-6, and IL-10 serum levels was observed in the GK-1/anti-PD-L1 combination group that may explain the beneficial effects of the combination treatment in prolonging the life of mice bearing melanoma. The data indicate that GK-1/anti-PD-L1 combined therapy affectively increases survival and warrants further clinical investigations.
转移性黑色素瘤新疗法的近期进展,如丝裂原活化蛋白激酶途径抑制剂、抗细胞毒性T淋巴细胞相关抗原4以及程序性细胞死亡蛋白1/程序性细胞死亡配体1(PD-L1)途径阻断抗体,还有联合治疗策略,均取得了令人鼓舞的成果,改变了黑色素瘤患者不断演变的治疗选择格局。一种有前景的新治疗方式是基于使用免疫调节单克隆抗体,这类抗体可增强抗肿瘤免疫反应成分(如T细胞)的功能,或阻断抑制有效抗肿瘤免疫的免疫检查点。程序性死亡-1受体及其配体PD-L1是肿瘤抑制T细胞介导的抗肿瘤免疫反应的主要机制。对小鼠的研究表明,来自肥胖带绦虫囊尾蚴的一种18个氨基酸的肽GK-1,有潜力通过刺激促炎细胞因子用作癌症治疗的主要或辅助成分。作者推测,GK-1与抗PD-L1联合治疗将提高荷黑色素瘤肿瘤小鼠的存活率。将C57BL/6小鼠注射B16-F10-luc2细胞,并分为四组:对照组、GK-1组、抗PD-L1组和GK-1/抗PD-L1组。使用卡尺和生物发光法测量并监测肿瘤大小。与其他组(23 - 27天)相比,GK-1肽与抗PD-L1联合使用显示出显著更长的生存期(34天)。这意味着生存期有所增加;接受GK-1 +抗PD-L1治疗的小鼠生存期增加了47.82%,单独接受GK-1治疗的小鼠增加了21.7%,仅接受抗PD-L1治疗的小鼠增加了6.08%。在第0天、第14天以及安乐死或实验结束时采集血样,使用小鼠特异性V-PLEX促炎细胞因子检测板监测细胞因子。在GK-1/抗PD-L1联合治疗组中观察到肿瘤坏死因子-α、白细胞介素-4、白细胞介素-5、白细胞介素-6和白细胞介素-10血清水平降低,这可能解释了联合治疗对延长荷黑色素瘤小鼠寿命的有益作用。数据表明,GK-1/抗PD-L1联合疗法有效地提高了存活率,值得进一步开展临床研究。