Department of Microbiology and Immunology, McGill University, Montréal, Canada.
Infectious Diseases and Immunity in Global Health Program, Research Institute of the McGill University Health Centre, Montréal, Canada.
Sci Rep. 2020 Apr 3;10(1):5874. doi: 10.1038/s41598-020-62543-5.
Complete Freund's adjuvant (CFA) has historically been one of the most useful tools of immunologists. Essentially comprised of dead mycobacteria and mineral oil, we asked ourselves what is special about the mycobacterial part of this adjuvant, and could it be recapitulated synthetically? Here, we demonstrate the essentiality of N-glycolylated peptidoglycan plus trehalose dimycolate (both unique in mycobacteria) for the complete adjuvant effect using knockouts and chemical complementation. A combination of synthetic N-glycolyl muramyl dipeptide and minimal trehalose dimycolate motif GlcC14C18 was able to upregulate dendritic cell effectors, plus induce experimental autoimmunity qualitatively similar but quantitatively milder compared to CFA. This research outlines how to substitute CFA with a consistent, molecularly-defined adjuvant which may inform the design of immunotherapeutic agents and vaccines benefitting from cell-mediated immunity. We also anticipate using synthetic microbe-associated molecular patterns (MAMPs) to study mycobacterial immunity and immunopathogenesis.
完全弗氏佐剂(CFA)一直是免疫学家最有用的工具之一。它本质上由死分枝杆菌和矿物油组成,我们想知道这种佐剂中分枝杆菌部分有什么特别之处,能否通过合成来重现?在这里,我们使用基因敲除和化学互补的方法证明了 N-糖基化肽聚糖加海藻糖二没食子酸酯(两者在分枝杆菌中都是独特的)对于完全佐剂效应的必要性。合成的 N-糖基化胞壁酰二肽和最小的海藻糖二没食子酸酯基序 GlcC14C18 的组合能够上调树突状细胞效应器,并且与 CFA 相比,能够诱导定性相似但定量更温和的实验性自身免疫。这项研究概述了如何用一种一致的、分子定义明确的佐剂替代 CFA,这可能为受益于细胞介导免疫的免疫治疗剂和疫苗的设计提供信息。我们还预计使用合成的微生物相关分子模式(MAMPs)来研究分枝杆菌免疫和免疫发病机制。