SPA14 脂质体结合了皂苷和全合成 TLR4 激动剂,为候选 hCMV 疫苗提供了佐剂性。

IF 6.9 1区 医学 Q1 IMMUNOLOGY
Ernesto Luna, Sophie Ruiz, Marie Garinot, Cyril Chavagnac, Pankaj Agrawal, John Escobar, Laurent Revet, Marie-Jeanne Asensio, Fabienne Piras, Francis G Fang, Donald R Drake, Bachra Rokbi, Daniel Larocque, Jean Haensler
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引用次数: 0

摘要

为了设计和开发一种新的基于皂苷的佐剂体系,我们将QS21皂苷与低微克量的全合成TLR4激动剂E6020结合在含胆固醇脂质体中。在pH 6.0-6.5的柠檬酸缓冲液中配制的佐剂体系称为SPA14,是一种长期稳定且均匀的悬浮液,主要由单层和少量多层囊泡组成,平均水动力直径为93 nm。在体外人先天免疫构建体中,将SPA14与GSK的QS21/MPL®脂质体佐剂系统AS01B进行比较,并以QS21-脂质体为基准,基于抗原呈递细胞(APC)激活和细胞因子分泌,SPA14显示出最强的免疫刺激潜力,这主要是由高活性的E6020激动剂驱动的。当以人巨细胞病毒糖蛋白B (gB)和五聚体复合物(PC)作为试验抗原进行体内佐剂试验时,在小鼠和非人灵长类动物(NHPs)中,SPA14通常具有良好的耐受性,并且与AS01B一样具有诱导长效cmv中和抗体的活性。两种佐剂均促进了基于小鼠IgG2c产生和小鼠IFN-γ产生和NHPs的Th-1反应的诱导,但在小鼠中,SPA14获得了更高水平的Th-2细胞因子(IL-5)和更高的IgG1 / IgG2c分泌细胞比例,这表明SPA14的佐剂谱可能比AS01B更少地偏向于Th-1。从可展性的角度来看,由于包括E6020在内的所有脂质组分在乙醇中的高溶解度,SPA14可以通过一种简单且可扩展的乙醇注射方法制备。此外,E6020是一种单分子、特性良好的全合成TLR4激动剂,通过优化的高产率合成路线,以全结晶起始材料和中间体为原料,经过8个合成步骤构建而成。总的来说,我们的数据表明,SPA14是一种可行的、易于制造的、有效的新型佐剂体系,可以广泛应用于长期稳定的液体制剂形式的即拌佐剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SPA14 liposomes combining saponin with fully synthetic TLR4 agonist provide adjuvanticity to hCMV vaccine candidate.

In the aim of designing and developing a novel saponin-based adjuvant system, we combined the QS21 saponin with low microgram amounts of the fully synthetic TLR4 agonist, E6020, in cholesterol-containing liposomes. The resulting adjuvant system, termed SPA14, appeared as a long-term stable and homogeneous suspension of mostly unilamellar and a few multilamellar vesicles, with an average hydrodynamic diameter of 93 nm, when formulated in citrate buffer at pH 6.0-6.5. When compared in an in vitro human innate immunity construct to AS01B, the QS21/MPL® liposomal adjuvant system of GSK, and with QS21-Liposomes used as benchmarks, SPA14 displayed the strongest immunostimulatory potential based on antigen-presenting cell (APC) activation and cytokine secretion, which was essentially driven by the highly active E6020 agonist in this assay. When tested as an adjuvant in vivo with human cytomegalovirus glycoprotein B (gB) and pentamer complex (PC) as test antigens, SPA14 was generally well tolerated and as active as AS01B for the induction of long-lasting CMV-neutralizing antibodies in mice and non-human primates (NHPs). Both adjuvants promoted the induction of Th-1 responses based on IgG2c production in mice and IFN-γ production in mice and NHPs, but in mice, a higher level of Th-2 cytokines (IL-5) and higher IgG1 over IgG2c secreting cells ratios were obtained with SPA14 indicating that the adjuvant profile of SPA14 could be less Th-1 biased than that of AS01B. From a developability standpoint, SPA14 could be manufactured by a simple and scalable ethanol injection method, owing to the high solubility in ethanol of all its lipidic components, including E6020. Furthermore, E6020 is a single molecule, well-characterized fully synthetic TLR4 agonist constructed in eight synthetic steps from entirely crystalline starting materials and intermediates via an optimized high-yield synthetic route. Overall, our data suggest that SPA14 is a viable, easy-to-manufacture, potent novel adjuvant system that could be broadly applicable as a ready-to-mix adjuvant in the form of a long-term stable liquid formulation.

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来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
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