Departments of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute, La Jolla, California 92037, United States.
Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, Maryland 20850, United States.
Mol Pharm. 2022 Sep 5;19(9):3358-3366. doi: 10.1021/acs.molpharmaceut.2c00489. Epub 2022 Aug 19.
Cocaine is a highly addictive drug that has seen a steady uptrend causing severe health problems worldwide. Currently, there are no approved therapeutics for treating cocaine use disorder; hence, there is an urgent need to identify new medications. Immunopharmacotherapeutics is a promising approach utilizing endogenous antibodies generated through active vaccination, and if properly programmed, can blunt a drug's psychoactive and addictive effects. However, drug vaccine efficacy has largely been limited by the modest levels of antibodies induced. Herein, we explored an adjuvant system consisting of a polyphosphazene macromolecule, specifically poly[di(carboxylatoethylphenoxy)-phosphazene] (PCEP), a biocompatible synthetic polymer that was solicited for improved cocaine conjugate vaccine delivery performance. Our results demonstrated PCEP's superior assembling efficiency with a cocaine hapten as well as with the combined adjuvant CpG oligodeoxynucleotide (ODN). Importantly, this combination led to a higher titer response, balanced immunity, successful sequestering of cocaine in the blood, and a reduction in the drug in the brain. Moreover, a PCEP-cocaine conjugate vaccine was also found to function well via intranasal administration, where its efficacy was demonstrated through the antibody titer, affinity, mucosal IgA production, and a reduction in cocaine's locomotor activity. Overall, a comprehensive evaluation of PCEP integrated within a cocaine vaccine established an advance in the use of synthetic adjuvants in the drugs of abuse vaccine field.
可卡因是一种高度成瘾的毒品,在全球范围内导致严重的健康问题。目前,尚无治疗可卡因使用障碍的批准疗法;因此,迫切需要确定新的药物。免疫药理学是一种很有前途的方法,它利用主动接种产生的内源性抗体,如果经过适当的编程,可以减轻药物的致幻和成瘾作用。然而,药物疫苗的疗效在很大程度上受到诱导的抗体水平的限制。在此,我们探索了一种由聚膦腈大分子组成的佐剂系统,特别是聚[双(羧基乙酯苯氧基)膦腈](PCEP),这是一种生物相容性的合成聚合物,旨在提高可卡因缀合物疫苗的递送性能。我们的研究结果表明,PCEP 与可卡因半抗原以及联合佐剂 CpG 寡脱氧核苷酸(ODN)具有优越的组装效率。重要的是,这种组合导致更高的效价反应、平衡的免疫、可卡因在血液中的成功隔离以及大脑中药物的减少。此外,还发现 PCEP-可卡因缀合物疫苗通过鼻内给药也能很好地发挥作用,其通过抗体效价、亲和力、黏膜 IgA 产生以及可卡因运动活性的降低来证明其疗效。总的来说,对可卡因疫苗中包含的 PCEP 的全面评估确立了在滥用药物疫苗领域中使用合成佐剂的进展。