Yan Hongbin, Chen Wangxue
Department of Chemistry, Brock University, St. Catharines, ON L2S 3A1, Canada.
Human Health and Therapeutics Research Centre, National Research Council Canada, Ottawa, ON K1A 0R6, Canada.
Vaccines (Basel). 2021 Aug 17;9(8):917. doi: 10.3390/vaccines9080917.
Cyclic dinucleotides (CDNs), originally discovered as bacterial second messengers, play critical roles in bacterial signal transduction, cellular processes, biofilm formation, and virulence. The finding that CDNs can trigger the innate immune response in eukaryotic cells through the stimulator of interferon genes (STING) signalling pathway has prompted the extensive research and development of CDNs as potential immunostimulators and novel molecular adjuvants for induction of systemic and mucosal innate and adaptive immune responses. In this review, we summarize the chemical structure, biosynthesis regulation, and the role of CDNs in enhancing the crosstalk between host innate and adaptive immune responses. We also discuss the strategies to improve the efficient delivery of CDNs and the recent advance and future challenges in the development of CDNs as potential adjuvants in prophylactic vaccines against infectious diseases and in therapeutic vaccines against cancers.
环二核苷酸(CDNs)最初作为细菌第二信使被发现,在细菌信号转导、细胞过程、生物膜形成和毒力方面发挥着关键作用。CDNs可通过干扰素基因刺激物(STING)信号通路触发真核细胞的先天免疫反应,这一发现促使人们对CDNs作为潜在免疫刺激剂和新型分子佐剂进行广泛研究和开发,以诱导全身和黏膜先天及适应性免疫反应。在本综述中,我们总结了CDNs的化学结构、生物合成调控及其在增强宿主先天免疫与适应性免疫反应之间相互作用中的作用。我们还讨论了提高CDNs有效递送的策略,以及CDNs作为预防传染病的预防性疫苗和抗癌治疗性疫苗的潜在佐剂开发方面的最新进展和未来挑战。