Saponin nanoparticle adjuvants incorporating Toll-like receptor agonists drive distinct immune signatures and potent vaccine responses.
Ben S OuJulie BailletMaria V Filsinger InterranteJulia Z AdamskaXueting ZhouOlivia M SaouafJerry YanJohn H KlichCarolyn K JonsEmily L MeanyAdian S ValdezLauren CarterBali PulendranNeil P KingEric A AppelPublished in: Science advances (2024)
Over the past few decades, the development of potent and safe immune-activating adjuvant technologies has become the heart of intensive research in the constant fight against highly mutative and immune evasive viruses such as influenza, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and human immunodeficiency virus (HIV). Herein, we developed a highly modular saponin-based nanoparticle platform incorporating Toll-like receptor agonists (TLRas) including TLR1/2a, TLR4a, and TLR7/8a adjuvants and their mixtures. These various TLRa-saponin nanoparticle adjuvant constructs induce unique acute cytokine and immune-signaling profiles, leading to specific T helper responses that could be of interest depending on the target disease for prevention. In a murine vaccine study, the adjuvants greatly improved the potency, durability, breadth, and neutralization of both COVID-19 and HIV vaccine candidates, suggesting the potential broad application of these adjuvant constructs to a range of different antigens. Overall, this work demonstrates a modular TLRa-SNP adjuvant platform that could improve the design of vaccines and affect modern vaccine development.
Keyphrases
- toll like receptor
- human immunodeficiency virus
- sars cov
- respiratory syndrome coronavirus
- antiretroviral therapy
- inflammatory response
- nuclear factor
- hepatitis c virus
- early stage
- hiv infected
- immune response
- hiv positive
- coronavirus disease
- hiv aids
- hiv testing
- heart failure
- dendritic cells
- high throughput
- genome wide
- signaling pathway
- atrial fibrillation
- ionic liquid
- risk assessment
- south africa
- climate change
- acute respiratory distress syndrome
- high density
- hepatitis b virus
- mechanical ventilation