Development of a Clinically Viable Heroin Vaccine

• Published in: Journal of the American Chemical Society Vol. 139; no. 25; pp. 8601 - 8611
• Main Authors: Bremer, Paul T, Schlosburg, Joel E, Banks, Matthew L, Steele, Floyd. F, Zhou, Bin, Poklis, Justin L, Janda, Kim D
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 28.06.2017; Amer Chemical Soc
• Subjects: adjuvants; Adjuvants, Immunologic - chemistry; alum; antibodies; antiserum; Chemistry; Chemistry, Multidisciplinary; cross reaction; Drug Design; haptens; Haptens - chemistry; Heroin; Immunity, Humoral; immunization; immunoglobulin G; Macaca mulatta; metabolites; mice; monkeys; narcotics; oligodeoxyribonucleotides; Physical Sciences; Science & Technology; surface plasmon resonance; vaccines; Vaccines, Conjugate; NONHUMAN-PRIMATES; SMOKING-CESSATION; THERAPEUTIC COCAINE VACCINE; CONJUGATE VACCINE; RHESUS-MONKEYS; DOUBLE-BLIND; PLACEBO-CONTROLLED TRIAL; ACTIVE IMMUNIZATION; CONTROLLED EFFICACY-TRIAL; ANTI-NICOTINE VACCINE
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.7b03334

Heroin is a highly abused opioid and incurs a significant detriment to society worldwide. In an effort to expand the limited pharmacotherapy options for opioid use disorders, a heroin conjugate vaccine was developed through comprehensive evaluation of hapten structure, carrier protein, adjuvant and dosing. Immunization of mice with an optimized heroin-tetanus toxoid (TT) conjugate formulated with adjuvants alum and CpG oligodeoxynucleotide (ODN) generated heroin “immunoantagonism”, reducing heroin potency by >15-fold. Moreover, the vaccine effects proved to be durable, persisting for over eight months. The lead vaccine was effective in rhesus monkeys, generating significant and sustained antidrug IgG titers in each subject. Characterization of both mouse and monkey antiheroin antibodies by surface plasmon resonance (SPR) revealed low nanomolar antiserum affinity for the key heroin metabolite, 6-acetylmorphine (6AM), with minimal cross reactivity to clinically used opioids. Following a series of heroin challenges over six months in vaccinated monkeys, drug-sequestering antibodies caused marked attenuation of heroin potency (>4-fold) in a schedule-controlled responding (SCR) behavioral assay. Overall, these preclinical results provide an empirical foundation supporting the further evaluation and potential clinical utility of an effective heroin vaccine in treating opioid use disorders.