Gamboa Marin Oscar Javier, Adda-Bouchard Yasmine, Sylla Balla, Verma Nitish, Charpentier Tania, Huber Maya, Lopez Guillaume, Pichette André, Lamarre Alain, Gauthier Charles
Centre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique (INRS), Laval, Québec, H7V 1B7, Canada.
Unité Mixte de Recherche (UMR) INRS-UQAC, Institut National de la Recherche Scientifique (INRS), Chicoutimi, Québec, G7H 2B1, Canada.
Chemistry. 2025 May 19;31(28):e202500994. doi: 10.1002/chem.202500994. Epub 2025 Apr 21.
The search for safer and more effective vaccine adjuvants has intensified in recent years, with triterpenoid saponins like QS-21 and its analogues emerging as promising candidates. We report the synthesis of a novel QS-21 analogue featuring betulinic acid as aglycone, a lupane-type triterpenoid with low toxicity derived from white birch bark. Two convergent synthetic routes, involving different protecting groups and glycosyl donors (bromide and trichloroacetimidate), were optimized to construct the QS-21-based linear trisaccharide motif critical for adjuvant activity. This strategy also enabled efficient preparation of the structurally similar echinocystic acid analogue reported by Gin. The immunological and toxicological profiles of these chimeric saponins, along with Lewis-X-containing and rhamnose-modified derivatives, were evaluated in C57BL/6 wild-type and hDC-SIGN transgenic mice. While the synthetic saponins exhibited low toxicity in vitro and in vivo, replacing echinocystic acid with betulinic acid reduced immunogenicity when tested with ovalbumin as a model antigen compared to alhydrogel and QS-21. These findings provide a foundation for developing saponin-based adjuvants and demonstrate the utility of advanced glycosylation strategies for synthesizing complex unnatural triterpenoid saponins.
近年来,对更安全、更有效的疫苗佐剂的研究不断加强,以齐墩果酸-21(QS-21)及其类似物为代表的三萜皂苷成为了有前景的候选物。我们报道了一种新型QS-21类似物的合成,该类似物以桦木酸为苷元,桦木酸是一种从白桦树皮中提取的毒性较低的羽扇豆烷型三萜。优化了两条汇聚合成路线,它们涉及不同的保护基团和糖基供体(溴化物和三氯乙酰亚胺酯),以构建对佐剂活性至关重要的基于QS-21的线性三糖基序。该策略还实现了高效制备Gin报道的结构相似的echinocystic酸类似物。在C57BL/6野生型和hDC-SIGN转基因小鼠中评估了这些嵌合皂苷以及含Lewis-X和鼠李糖修饰衍生物的免疫和毒理学特性。虽然合成皂苷在体外和体内均表现出低毒性,但与氢氧化铝凝胶和QS-21相比,以卵清蛋白作为模型抗原进行测试时,用桦木酸替代echinocystic酸会降低免疫原性。这些发现为开发基于皂苷的佐剂奠定了基础,并证明了先进糖基化策略在合成复杂的非天然三萜皂苷方面的实用性。