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Development of a Clinically Viable Heroin Vaccine.
Bremer, Paul T; Schlosburg, Joel E; Banks, Matthew L; Steele, Floyd F; Zhou, Bin; Poklis, Justin L; Janda, Kim D.
Afiliação
  • Bremer PT; Departments of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute , 10550 N Torrey Pines Road, La Jolla, California 92037, United States.
  • Schlosburg JE; Department of Pharmacology and Toxicology, Virginia Commonwealth University , 410 N 12th Street, Richmond, Virginia 23298, United States.
  • Banks ML; Department of Pharmacology and Toxicology, Virginia Commonwealth University , 410 N 12th Street, Richmond, Virginia 23298, United States.
  • Steele FF; Department of Pharmacology and Toxicology, Virginia Commonwealth University , 410 N 12th Street, Richmond, Virginia 23298, United States.
  • Zhou B; Departments of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute , 10550 N Torrey Pines Road, La Jolla, California 92037, United States.
  • Poklis JL; Department of Pharmacology and Toxicology, Virginia Commonwealth University , 410 N 12th Street, Richmond, Virginia 23298, United States.
  • Janda KD; Departments of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute , 10550 N Torrey Pines Road, La Jolla, California 92037, United States.
J Am Chem Soc ; 139(25): 8601-8611, 2017 06 28.
Article em En | MEDLINE | ID: mdl-28574716
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article