A Self-Amplifying Human Papillomavirus 16 Vaccine Candidate Delivered by Tobacco Mosaic Virus-Like Particles
Virus-like particles (VLPs) are naturally occurring delivery platforms with potential for mRNA vaccines that can be used as an alternative to lipid nanoparticles. Here we describe a self-amplifying mRNA vaccine based on tobacco mosaic virus (TMV) expressing a mutated E7 protein from human papillomavirus 16 (HPV16). E7 is an early gene that plays a central role in viral replication and the oncogenic transformation of host cells, but nononcogenic mutant E7 proteins can suppress this activity. Immunization studies involving the delivery of self-amplifying mutant E7 mRNA packaged with TMV coat proteins confirmed the elicitation of E7-specific IgG antibodies. Additional <i>in vitro</i> splenocyte proliferation and cytokine profiling assays indicated the activation of humoral and cellular immune responses. We conclude that TMV particles are suitable for the delivery of mRNA vaccines and can preserve their integrity and functionality <i>in vitro</i> and <i>in vivo</i>.
Authors
- Miguel A. Moreno‐Gonzalez (ORCID: https://orcid.org/0000-0002-1601-9369)
- Sweta Karan (ORCID: https://orcid.org/0000-0003-4989-313X)
- Nicole F. Steinmetz (ORCID: https://orcid.org/0000-0002-0130-0481)
- Jessica Fernanda Affonso de Oliveira (ORCID: https://orcid.org/0000-0002-5474-2355)
Institutions
- University of California San Diego (US)
Publication Details
- Journal
- ACS Applied Bio Materials
- Published
- 2024-11-08
- DOI
- https://doi.org/10.1021/acsabm.4c01239
- Citations
- 4
- Primary Topic
- Virus-based gene therapy research
- Type
- article
- Field-Weighted Citation Impact
- 2.20
Funders
- National Science Foundation
- National Institutes of Health
- University of California, San Diego
- National Cancer Institute
- Division of Chemical, Bioengineering, Environmental, and Transport Systems