免疫原
药理学
佐剂
化学
免疫药理学
体内
免疫系统
半抗原
上瘾
免疫学
抗体
医学
单克隆抗体
精神科
生物
生物技术
作者
Harrison Y. R. Madge,Suzy Alexander,Armira Azuar,Jiahui Zhang,Prashamsa Koirala,Thomas H.J. Burne,István Tóth,Rachel J. Stephenson
标识
DOI:10.1021/acs.jmedchem.3c00889
摘要
Cocaine is one of the most widely used and increasingly popular illicit psychoactive drugs. Unlike other commonly used substances of abuse, cocaine has no pharmacological therapies to treat addiction or aid in rehabilitation. Immunopharmacology has long been touted as a possible avenue to develop effective anticocaine therapies; however, lack of efficacy and designs which are not consistent with simple large-scale production have hindered vaccine translation. We have designed and synthesized a peptide-based anti-cocaine immunogen which we have shown is capable of inducing physiologically relevant immune responses in mice as part of a self-adjuvanting delivery system or in combination with the human-approved commercial adjuvant MF59. We have demonstrated that immunization with the reported vaccine elicits high titers of anti-cocaine IgG and prevents cocaine-induced hyperlocomotion in an in vivo murine model. This peptide-hapten immunogen along with self-adjuvanting liposomal-based delivery system provides a platform for the development of effective anti-drug vaccines.
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