A synthetic opioid vaccine attenuates fentanyl-vs-food choice in male and female rhesus monkeys.


Journal

Drug and alcohol dependence
ISSN: 1879-0046
Titre abrégé: Drug Alcohol Depend
Pays: Ireland
ID NLM: 7513587

Informations de publication

Date de publication:
01 01 2021
Historique:
received: 26 08 2020
revised: 24 09 2020
accepted: 24 09 2020
pubmed: 4 12 2020
medline: 29 5 2021
entrez: 3 12 2020
Statut: ppublish

Résumé

Opioid-targeted vaccines are under consideration as candidate Opioid Use Disorder medications. We recently reported that a fentanyl-targeted vaccine produced a robust and long-lasting attenuation of fentanyl-vs-food choice in rats. In the current study, we evaluated an optimized fentanyl-targeted vaccine in rhesus monkeys to determine whether vaccine effectiveness to attenuate fentanyl choice translated to a species with greater phylogenetic similarity to humans. Adult male (2) and female (3) rhesus monkeys were trained to respond under a concurrent schedule of food (1 g pellets) and intravenous fentanyl (0, 0.032-1 μg/kg/injection) reinforcement during daily 2 h sessions. Fentanyl choice dose-effect functions were determined daily and 7-day buprenorphine treatments (0.0032-0.032 mg/kg/h IV; n = 4-5) were determined for comparison to vaccine effects. Subsequently, a fentanyl-CRM Buprenorphine significantly decreased fentanyl choice and reciprocally increased food choice. Vaccination eliminated fentanyl choice and increased food choice in four-of-the-five monkeys. A transient and less robust vaccine effect was observed in the fifth monkey. Fentanyl-specific antibody concentrations peaked after the third vaccination to approximately 50 μg/mL while anti-fentanyl antibody affinity increased to a sustained low nanomolar level. These results translate fentanyl vaccine effectiveness from rats to rhesus monkeys to decrease fentanyl-vs-food choice, albeit with greater individual differences observed in monkeys. These results support the potential and further clinical evaluation of this fentanyl-targeted vaccine as a candidate Opioid Use Disorder medication.

Identifiants

pubmed: 33268227
pii: S0376-8716(20)30513-5
doi: 10.1016/j.drugalcdep.2020.108348
pmc: PMC8224470
mid: NIHMS1639081
pii:
doi:

Substances chimiques

Analgesics, Opioid 0
Vaccines 0
Fentanyl UF599785JZ

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

108348

Subventions

Organisme : NIDA NIH HHS
ID : F32 DA047026
Pays : United States
Organisme : NIDA NIH HHS
ID : UH3 DA041146
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

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Auteurs

E Andrew Townsend (EA)

Department of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, 23298, USA. Electronic address: Edward.townsend@vcuhealth.org.

Paul T Bremer (PT)

Cessation Therapeutics, San Jose, CA, 95128, USA; Departments of Chemistry and Immunology and Microbial Science, Skaggs Institute for Chemical Biology, Worm Institute for Research and Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.

Nicholas T Jacob (NT)

Cessation Therapeutics, San Jose, CA, 95128, USA.

S Stevens Negus (SS)

Department of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, 23298, USA.

Kim D Janda (KD)

Departments of Chemistry and Immunology and Microbial Science, Skaggs Institute for Chemical Biology, Worm Institute for Research and Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA. Electronic address: kdjanda@scripps.edu.

Matthew L Banks (ML)

Department of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, 23298, USA.

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Classifications MeSH