Ou Ben S, Baillet Julie, Filsinger Interrante Maria V, Adamska Julia Z, Zhou Xueting, Saouaf Olivia M, Yan Jerry, Klich John H, Jons Carolyn K, Meany Emily L, Valdez Adian S, Carter Lauren, Pulendran Bali, King Neil P, Appel Eric A
bioRxiv. 2024 Jun 27:2023.07.16.549249. doi: 10.1101/2023.07.16.549249.
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, SARS-CoV-2, and HIV. Herein, we developed a highly modular saponin-based nanoparticle platform incorporating toll-like receptor agonists (TLRas) including TLR1/2a, TLR4a, TLR7/8a adjuvants and their mixtures. These various TLRa-SNP adjuvant constructs induce unique acute cytokine and immune-signaling profiles, leading to specific Th-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 which could improve the design of vaccines for and dramatically impact modern vaccine development.
Saponin-TLRa nanoadjuvants provide distinct immune signatures and drive potent, broad, durable COVID-19 and HIV vaccine responses.
在过去几十年中,高效且安全的免疫激活佐剂技术的发展已成为对抗高度变异且能逃避免疫的病毒(如流感病毒、SARS-CoV-2和HIV)的密集研究的核心。在此,我们开发了一种高度模块化的基于皂苷的纳米颗粒平台,该平台包含Toll样受体激动剂(TLRas),包括TLR1/2a、TLR4a、TLR7/8a佐剂及其混合物。这些不同的TLRa-SNP佐剂构建体诱导独特的急性细胞因子和免疫信号谱,导致特定的Th反应,根据预防的目标疾病可能会引起关注。在一项小鼠疫苗研究中,这些佐剂极大地提高了COVID-19和HIV候选疫苗的效力、持久性、广度和中和能力,表明这些佐剂构建体在一系列不同抗原上具有广泛应用潜力。总体而言,这项工作展示了一个模块化的TLRa-SNP佐剂平台,该平台可改进疫苗设计并对现代疫苗开发产生重大影响。
皂苷-TLRa纳米佐剂提供独特的免疫特征,并驱动强效、广泛、持久的COVID-19和HIV疫苗反应。