UF Brain Tumor Immunotherapy Program, Preston A. Wells Jr. Center for Brain Tumor Therapy, Department of Neurosurgery, University of Florida, Gainesville, FL, USA.
J Immunol Res. 2017;2017:3145742. doi: 10.1155/2017/3145742. Epub 2017 Feb 6.
Although cancer immunotherapy has shown significant promise in mediating efficacious responses, it remains encumbered by tumor heterogeneity, loss of tumor-specific antigen targets, and the regulatory milieu both regionally and systemically. Cross talk between the innate and adaptive immune response may be requisite to polarize sustained antigen specific immunity. Cancer vaccines can serve as an essential fulcrum in initiating innate immunity while molding and sustaining adaptive immunity. Although peptide vaccines have shown tepid responses in a therapeutic setting with poor correlates for immune activity, RNA vaccines activate innate immune responses and have shown promising effects in preclinical and clinical studies based on enhanced DC migration. While the mechanistic insights behind the interplay between innate and adaptive immunity may be unique to the immunotherapeutic being investigated, understanding this dynamic is important to coordinate the different arms of the immune response in a focused response against cancer antigens.
虽然癌症免疫疗法在介导有效的反应方面显示出了显著的前景,但它仍然受到肿瘤异质性、肿瘤特异性抗原靶点的丢失以及局部和全身的调节环境的限制。先天免疫和适应性免疫反应之间的相互作用可能是极化持续的抗原特异性免疫所必需的。癌症疫苗可以作为启动先天免疫的重要支点,同时塑造和维持适应性免疫。虽然肽疫苗在治疗环境中表现出温和的反应,与免疫活性的相关性较差,但 RNA 疫苗激活先天免疫反应,并基于增强的 DC 迁移,在临床前和临床研究中显示出有希望的效果。虽然先天免疫和适应性免疫之间相互作用的机制见解可能是针对所研究的免疫疗法的独特的,但了解这种动态对于协调免疫反应的不同分支以针对癌症抗原进行集中反应是很重要的。