Hossain Md Kamal, Davidson Majid, Feehan Jack, Deraos George, Nurgali Kulmira, Matsoukas John, Apostolopoulos Vasso
Institute for Health and Sport, Victoria University, Melbourne, VIC 3030, Australia.
Regenerative Medicine and Stem Cells Program, Australian Institute for Musculoskeletal Science (AIMSS), Melbourne, VIC 3021, Australia.
Vaccines (Basel). 2023 Feb 2;11(2):340. doi: 10.3390/vaccines11020340.
Methamphetamine (METH) substance-use disorder is an ever-growing global health issue with no effective treatment. Anti-METH vaccines are under investigation as an alternative to existing psychological interventions. This platform has made significant progress over past decades mainly in preclinical stages, and efforts to develop an anti-METH vaccine with a high antibody response are of utmost importance.
A novel conjugated anti-METH vaccine was developed using METH HCl as the starting material for the design of hapten, a peptide linker consisting of five lysines and five glycines, and finally immunogenic carrier mannan, which is novel to this platform. All the chemical reaction steps were confirmed by several analytical techniques, and the immunogenicity of the developed vaccine was investigated in a mouse model.
Thin-layer chromatography and gas chromatography confirmed the reaction between METH and peptide linker. UV, NMR and color tests were used to confirm the presence of the aldehyde groups in oxidized mannan (OM). The final conjugated vaccine was confirmed by UV and LC-MS. The stability of mannan, the METH hapten, and the final vaccine was evaluated by UV and LC-MS and demonstrated satisfactory stability over 3 months in various storage conditions. Animal studies supported the immunogenicity of the novel vaccine.
We successfully developed and characterized a novel METH vaccine in vitro and in vivo. The present study findings are encouraging and will form the basis of further exploration to assess its effectiveness to prevent METH addiction in preclinical models.
甲基苯丙胺(METH)物质使用障碍是一个日益严重的全球健康问题,目前尚无有效治疗方法。抗METH疫苗正在作为现有心理干预措施的替代方法进行研究。在过去几十年中,该平台主要在临床前阶段取得了重大进展,开发具有高抗体反应的抗METH疫苗的努力至关重要。
以盐酸甲基苯丙胺为起始原料设计半抗原,采用由五个赖氨酸和五个甘氨酸组成的肽接头,最后使用对该平台而言新颖的免疫原性载体甘露聚糖,开发了一种新型共轭抗METH疫苗。所有化学反应步骤均通过多种分析技术进行确认,并在小鼠模型中研究了所开发疫苗的免疫原性。
薄层色谱法和气相色谱法证实了甲基苯丙胺与肽接头之间的反应。使用紫外光谱、核磁共振和颜色测试来确认氧化甘露聚糖(OM)中醛基的存在。最终的共轭疫苗通过紫外光谱和液相色谱 - 质谱进行确认。通过紫外光谱和液相色谱 - 质谱评估了甘露聚糖、甲基苯丙胺半抗原和最终疫苗的稳定性,结果表明在各种储存条件下,它们在3个月内具有令人满意的稳定性。动物研究支持了这种新型疫苗的免疫原性。
我们在体外和体内成功开发并表征了一种新型甲基苯丙胺疫苗。本研究结果令人鼓舞,并将为进一步探索评估其在临床前模型中预防甲基苯丙胺成瘾有效性的研究奠定基础。