Discovery of Self-Assembling Small Molecules as Vaccine Adjuvants.
Shuyu JinHue Thi VuKou HiokiNaotaka NodaHiroki YoshidaToru ShimaneShigenari IshizukaIppei TakashimaYoshiyuki MizuhataKathleen Beverly PeTetsuya OgawaNaoya NishimuraDaniel PackwoodNorihiro TokitohHiroki KurataSho YamasakiKen J IshiiMotonari UesugiPublished in: Angewandte Chemie (International ed. in English) (2020)
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.
Keyphrases
- immune response
- small molecule
- toll like receptor
- dendritic cells
- early stage
- nuclear factor
- protein protein
- single cell
- cell cycle arrest
- sars cov
- regulatory t cells
- inflammatory response
- gram negative
- bone marrow
- nucleic acid
- binding protein
- skeletal muscle
- adipose tissue
- high fat diet induced
- high throughput
- cell proliferation
- antimicrobial resistance
- multidrug resistant
- pi k akt
- oxidative stress
- insulin resistance
- signaling pathway
- metabolic syndrome