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A methamphetamine vaccine using short monoamine and diamine peptide linkers and poly-mannose

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posted on 2025-10-27, 04:56 authored by MK Hossain, M Davidson, Jack FeehanJack Feehan, JM Matsoukas, K Nurgali, Vasso ApostolopoulosVasso Apostolopoulos
Methamphetamine (METH) substance use disorder is a long-standing and ever-growing public health concern. Efforts to develop successful immunotherapies are ongoing with vaccines that generate strong antibody responses are an area of significant research interest. Herein, we describe the development of a METH Hapten conjugate vaccine comprised of either two short-length peptides as linkers and mannan as an immunogenic delivery carrier. Initially, Hapten 1 (with a monoamine linker) and Hapten 2 (with a diamine linker) were synthesised. Each step of the Hapten synthesis were characterized by LC-MS and purified by Flash Chromatography and the identity of the purified Haptens were confirmed by 1H NMR. Haptens were conjugated with mannan (a polymannose), and conjugation efficiency was confirmed by LC-MS, TLC, 1H NMR, and 2,4 DNPH tests. The immunogenic potential of the two conjugated vaccines were assessed in mice with a 3-dose regimen. Concentrations of anti-METH antibodies were measured by enzyme-linked immunosorbent assay. All the analytical techniques confirmed the identity of Hapten 1 and 2 during the synthetic phase. Similarly, all the analytical approaches confirmed the conjugation between the Haptens and mannan. Mouse immunogenicity studies confirmed that both vaccine candidates were immunogenic and the vaccine with the monoamine linker plus adjuvants induced the highest antibody response after the second booster.<p></p>

Funding

EW Scripps Co

History

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Journal

Bioorganic and Medicinal Chemistry

Volume

113

Number

117930

Total pages

14

Publisher

Elsevier

Language

eng

Copyright

© 2024 The Authors.

UN Sustainable Development Goals

  • 3 Good Health and Well Being

Open access

  • Yes