Institute for Health and Sport, Victoria University, Immunology and Translational Research Group, Werribee, VIC 3030, Australia; Scripps Research Institute, 10550 N Torrey Pines Rd, La Jolla, CA 92037, United States.
Institute for Health and Sport, Victoria University, Immunology and Translational Research Group, Werribee, VIC 3030, Australia.
Bioorg Med Chem. 2024 Nov 1;113:117930. doi: 10.1016/j.bmc.2024.117930. Epub 2024 Sep 19.
Methamphetamine (METH) substance use disorder is a long-standing and ever-growing public health concern. Efforts to develop successful immunotherapies are ongoing with vaccines that generate strong antibody responses are an area of significant research interest. Herein, we describe the development of a METH Hapten conjugate vaccine comprised of either two short-length peptides as linkers and mannan as an immunogenic delivery carrier. Initially, Hapten 1 (with a monoamine linker) and Hapten 2 (with a diamine linker) were synthesised. Each step of the Hapten synthesis were characterized by LC-MS and purified by Flash Chromatography and the identity of the purified Haptens were confirmed by H NMR. Haptens were conjugated with mannan (a polymannose), and conjugation efficiency was confirmed by LC-MS, TLC, H NMR, and 2,4 DNPH tests. The immunogenic potential of the two conjugated vaccines were assessed in mice with a 3-dose regimen. Concentrations of anti-METH antibodies were measured by enzyme-linked immunosorbent assay. All the analytical techniques confirmed the identity of Hapten 1 and 2 during the synthetic phase. Similarly, all the analytical approaches confirmed the conjugation between the Haptens and mannan. Mouse immunogenicity studies confirmed that both vaccine candidates were immunogenic and the vaccine with the monoamine linker plus adjuvants induced the highest antibody response after the second booster.
甲基苯丙胺(METH)物质使用障碍是一个长期存在且不断增长的公共卫生问题。正在努力开发成功的免疫疗法,具有强烈抗体反应的疫苗是一个重要的研究领域。在此,我们描述了一种由两个短肽作为接头和甘露聚糖作为免疫原性载体组成的 METH 半抗原缀合疫苗的开发。最初,合成了半抗原 1(具有单胺接头)和半抗原 2(具有二胺接头)。半抗原合成的每一步都通过 LC-MS 进行了表征,并通过快速色谱法进行了纯化,并且通过 1 H NMR 确认了纯化半抗原的身份。半抗原与甘露聚糖(多甘露糖)缀合,通过 LC-MS、TLC、1 H NMR 和 2,4-DNPH 测试确认缀合效率。用 3 剂方案在小鼠中评估了两种缀合疫苗的免疫原性。通过酶联免疫吸附试验测量抗 METH 抗体的浓度。所有分析技术都在合成阶段确认了半抗原 1 和 2 的身份。同样,所有分析方法都证实了半抗原与甘露聚糖之间的缀合。小鼠免疫原性研究证实,两种候选疫苗均具有免疫原性,并且含有单胺接头和佐剂的疫苗在第二次加强后诱导了最高的抗体反应。