Yu Ting-Wei, Chueh Ho-Yen, Tsai Ching-Chou, Lin Cheng-Tao, Qiu Jiantai Timothy
a School of Medicine , Chang Gung University , Taoyuan , Taiwan , ROC.
b Department of Obstetrics and Gynecology , Chang Gung Memorial Hospital , Taoyuan , Taiwan , ROC.
Hum Vaccin Immunother. 2016 Dec;12(12):3020-3028. doi: 10.1080/21645515.2016.1221551. Epub 2016 Aug 25.
Granulocyte macrophage-colony stimulating factor (GM-CSF) is a potent immunomodulatory cytokine that is known to facilitate vaccine efficacy by promoting the development and prolongation of both humoral and cellular immunity. In the past years we have generated a novel codon-optimized GM-CSF gene as an adjuvant. The codon-optimized GM-CSF gene significantly increased protein expression levels in all cells tested and helped in generating a strong immune responses against HIV-1 Gag and HPV-associated cancer. Here, we review the literature dealing with the adjuvant activity of GM-CSF both in animal models and clinical trials. We anticipate that the codon-optimized GM-CSF gene offers a practical molecular strategy for potentiating immune responses to tumor cell-based vaccinations as well as other immunotherapeutic strategies.
粒细胞巨噬细胞集落刺激因子(GM-CSF)是一种强效免疫调节细胞因子,已知其可通过促进体液免疫和细胞免疫的发展及延长来提高疫苗效力。在过去几年中,我们构建了一种新型的密码子优化GM-CSF基因作为佐剂。该密码子优化GM-CSF基因显著提高了在所有测试细胞中的蛋白质表达水平,并有助于产生针对HIV-1 Gag和HPV相关癌症的强烈免疫反应。在此,我们综述了有关GM-CSF在动物模型和临床试验中的佐剂活性的文献。我们预计,密码子优化GM-CSF基因提供了一种实用的分子策略,可增强对基于肿瘤细胞的疫苗接种以及其他免疫治疗策略的免疫反应。