School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.
Institute for Molecular Bioscience, The University of Queensland, St. Lucia, QLD 4072, Australia.
Bioorg Med Chem Lett. 2021 May 15;40:127920. doi: 10.1016/j.bmcl.2021.127920. Epub 2021 Mar 9.
We recently reported that polyethylenimine (PEI; molecular weight of 600 Da) acted as a vaccine adjuvant for liposomal group A Streptococcus (GAS) vaccines, eliciting immune responses in vivo with IgG antibodies giving opsonic activity against five Australian GAS clinical isolates. However, to date, no investigation comparing the structure-activity relationship between the molecular weight of PEI and its adjuvanting activity in vaccine development has been performed. We hypothesized that the molecular weight and quantity of PEI in a liposomal vaccine will impact its adjuvanting properties. In this study, we successfully formulated liposomes containing different molecular weights of PEI (600, 1800, 10k and 25k Da) and equivalents of PEI (0.5, 1 and 2) of branched PEI. Outbred mice were administrated the vaccine formulations intranasally, and the mice that received a high ratio of PEI 600 reported a stronger immune response than the mice that received a lower ratio of PEI 600. Interestingly, mice that received the same quantity of PEI 600, PEI 10k and PEI 25k showed similar immune responses in vivo and in vitro. This comparative study highlights the ratio of PEI present in the liposome vaccines impacts adjuvanting activity, however, PEI molecular weight did not significantly enhance its adjuvanting properties. We also report that the stability of PEI liposomes is critical for vaccines to elicit the desired immune response.
我们最近报道称,聚乙二烯亚胺(PEI;分子量为 600 Da)可作为脂质体 A 组溶血性链球菌(GAS)疫苗的佐剂,在体内引发免疫应答,产生针对 5 种澳大利亚 GAS 临床分离株具有调理活性的 IgG 抗体。然而,迄今为止,尚未对 PEI 的分子量与其在疫苗开发中的佐剂活性之间的构效关系进行比较研究。我们假设脂质体疫苗中 PEI 的分子量和数量将影响其佐剂特性。在这项研究中,我们成功地制备了含有不同分子量的 PEI(600、1800、10k 和 25k Da)和分支 PEI 的等效物(0.5、1 和 2)的脂质体。近交系小鼠经鼻腔给予疫苗制剂,接受高比例 PEI 600 的小鼠比接受低比例 PEI 600 的小鼠报告了更强的免疫应答。有趣的是,接受相同数量的 PEI 600、PEI 10k 和 PEI 25k 的小鼠在体内和体外表现出相似的免疫应答。这项比较研究强调了脂质体疫苗中存在的 PEI 比例会影响佐剂活性,但是,PEI 分子量并没有显著增强其佐剂特性。我们还报告称,PEI 脂质体的稳定性对于引发所需免疫应答的疫苗至关重要。