Two doses of Qβ virus like particle vaccines elicit protective antibodies against heroin and fentanyl

Opioid overdoses and opioid use disorder (OUD) are major public health concerns. Current treatment approaches for OUD have failed to slow the growth of the opioid crisis. Opioid vaccines have shown pre-clinical success in targeting multiple different opioid drugs. However, the need for many immunizations can limit their clinical implementation. In this study, we investigate the development of novel opioid vaccines by independently targeting fentanyl and the active metabolites of heroin using a bacteriophage virus-like particle (VLP) vaccine platform. We establish the successful conjugation of haptens to bacteriophage Qβ VLPs and demonstrate immunogenicity of Qβ-fentanyl, Qβ-morphine, and Qβ-6-acetylmorphine in animal models after one or two immunizations. We show that these vaccines elicit high-titer, high-avidity, and durable antibody responses. Moreover, we reveal their protective capacities against heroin or fentanyl challenge after two immunizations. Overall, these findings establish Qβ-VLP conjugated vaccines for heroin and fentanyl as promising opioid vaccine candidates.

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Publication Details

Journal
npj Vaccines
Published
2025-03-28
DOI
https://doi.org/10.1038/s41541-025-01105-0
Citations
2
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
2.71

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article

Two doses of Qβ virus like particle vaccines elicit protective antibodies against heroin and fentanyl

Brandi T. Johnson‐Weaver, William C. Wetsel, Marcus F. Brackeen, Susan B. Core et al.
2 citations
npj Vaccines
Influenza Virus Research Studies
2.71
article

Two doses of Qβ virus like particle vaccines elicit protective antibodies against heroin and fentanyl

Brandi T. Johnson‐Weaver, William C. Wetsel, Marcus F. Brackeen, Susan B. Core, Bryce Chackerian, Herman F. Staats, Yumei Huang, Bruce E. Blough, Kathryn M. Frietze, Andzoa N. Jamus, Isabella G. Romano, Subhakar Dey
article en
2 citations

Abstract

Opioid overdoses and opioid use disorder (OUD) are major public health concerns. Current treatment approaches for OUD have failed to slow the growth of the opioid crisis. Opioid vaccines have shown pre-clinical success in targeting multiple different opioid drugs. However, the need for many immunizations can limit their clinical implementation. In this study, we investigate the development of novel opioid vaccines by independently targeting fentanyl and the active metabolites of heroin using a bacteriophage virus-like particle (VLP) vaccine platform. We establish the successful conjugation of haptens to bacteriophage Qβ VLPs and demonstrate immunogenicity of Qβ-fentanyl, Qβ-morphine, and Qβ-6-acetylmorphine in animal models after one or two immunizations. We show that these vaccines elicit high-titer, high-avidity, and durable antibody responses. Moreover, we reveal their protective capacities against heroin or fentanyl challenge after two immunizations. Overall, these findings establish Qβ-VLP conjugated vaccines for heroin and fentanyl as promising opioid vaccine candidates.

npj VaccinesVol. 10(1)
University of New Mexico (US), Duke University (US), RTI International (US), CellMosaic (United States) (US)
National Institute on Drug Abuse, National Center for Advancing Translational Sciences
Zero hunger
Openalex Percentile: Top 11%
Influenza Virus Research Studies
2.71
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