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Published Online: 6 May 2024

Vaccines as Immunotherapies for Substance Use Disorders

Publication: American Journal of Psychiatry

Abstract

Substance use disorders (SUD) present a worldwide challenge with few effective therapies except for the relative efficacy of opioid pharmacotherapies, despite limited treatment access. However, the proliferation of illicit fentanyl use initiated a dramatic and cascading epidemic of lethal overdoses. This rise in fentanyl overdoses regenerated an interest in vaccine immunotherapy, which, despite an optimistic start in animal models over the past 50 years, yielded disappointing results in human clinical trials of vaccines against nicotine, stimulants (cocaine and methamphetamine), and opioids. After a brief review of clinical and selected preclinical vaccine studies, the “lessons learned” from the previous vaccine clinical trials are summarized, and then the newest challenge of a vaccine against fentanyl and its analogs is explored. Animal studies have made significant advances in vaccine technology for SUD treatment over the past 50 years, and the resulting anti-fentanyl vaccines show remarkable promise for ending this epidemic of fentanyl deaths.

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Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 362 - 371

History

Received: 17 October 2023
Revision received: 17 December 2023
Revision received: 13 February 2024
Accepted: 16 February 2024
Published in print: May 01, 2024
Published online: 6 May 2024

Keywords

  1. Substance-Related and Addictive Disorders
  2. Opioids
  3. Pharmacotherapy
  4. Immune Function
  5. Stimulants
  6. Nicotine

Authors

Details

Thomas R. Kosten, M.D. [email protected]
Waggoner Professor of Psychiatry, Pharmacology, Neuroscience, Immunology, Baylor College of Medicine, Houston.

Notes

Send correspondence to Dr. Kosten ([email protected]).

Competing Interests

The author reports serving as a consultant to Relmada Pharma about DEA scheduling of their antidepressant that is derived from methadone, a DEA schedule 2 medication.

Funding Information

No grant support contributed to this work.

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