| Literature DB >> 33536438 |
Ashley L St John1,2,3,4, Hae Woong Choi2,5, Q David Walker6, Bruce Blough7, Cynthia M Kuhn6, Soman N Abraham1,2,8,9, Herman F Staats10,11,12.
Abstract
Cocaine is one of the most potent and addictive psychostimulants known and there are no available pharmacotherapies to treat cocaine addiction. Here we describe a novel cocaine vaccine employing the mucosal adjuvant and mast cell-activating oligopeptide, mastoparan-7 (M7), to achieve optimal IgA antibody responses in mucosal secretions and effective induction of humoral immunity using a short immunization protocol. This formulation, using a hapten-carrier system to deliver cocaine as antigen, also reduced cocaine penetration of the blood brain barrier and protected mice from its psychoactive effects by reducing cocaine-induced locomotion. Surprisingly, the magnitude of cocaine-specific antibody titers induced by each adjuvant was not the major determinant of functional protection from cocaine challenge. A side-by-side comparison of the two haptens, cocaine and its analog GNC demonstrated that cocaine haptenation resulted in superior functional protection when used in combination with the novel mucosal adjuvant, M7. These results provide a new potential strategy for combatting cocaine addiction through mucosal vaccination.Year: 2020 PMID: 33536438 DOI: 10.1038/s41541-020-0161-1
Source DB: PubMed Journal: NPJ Vaccines ISSN: 2059-0105 Impact factor: 7.344