| Literature DB >> 32979004 |
Shuyu Jin1,2, Hue Thi Vu1,2, Kou Hioki3,4,5, Naotaka Noda1,2, Hiroki Yoshida1,2, Toru Shimane6, Shigenari Ishizuka6, Ippei Takashima2, Yoshiyuki Mizuhata2, Kathleen Beverly Pe1,2, Tetsuya Ogawa2, Naoya Nishimura6, Daniel Packwood7, Norihiro Tokitoh2, Hiroki Kurata2, Sho Yamasaki6, Ken J Ishii3,4,5, Motonari Uesugi2,7,8.
Abstract
Immune potentiators, termed adjuvants, trigger early innate immune responses to ensure the generation of robust and long-lasting adaptive immune responses of vaccines. Presented here is a study that takes advantage of a self-assembling small-molecule library for the development of a novel vaccine adjuvant. Cell-based screening of the library and subsequent structural optimization led to the discovery of a simple, chemically tractable deoxycholate derivative (molecule 6, also named cholicamide) whose well-defined nanoassembly potently elicits innate immune responses in macrophages and dendritic cells. Functional and mechanistic analyses indicate that the virus-like assembly enters the cells and stimulates the innate immune response through Toll-like receptor 7 (TLR7), an endosomal TLR that detects single-stranded viral RNA. As an influenza vaccine adjuvant in mice, molecule 6 was as potent as Alum, a clinically used adjuvant. The studies described here pave the way for a new approach to discovering and designing self-assembling small-molecule adjuvants against pathogens, including emerging viruses.Entities:
Keywords: RNA; chemical biology; nanostructures; self-assembly; viruses
Year: 2020 PMID: 32979004 DOI: 10.1002/anie.202011604
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336