An HTLV-1 envelope mRNA vaccine is immunogenic and protective in New Zealand rabbits

Author:

Tu Joshua J.1,King Emily1,Maksimova Victoria1,Smith Susan1,Macias Ramon2,Cheng Xiaogang3,Vegesna Tanmayee4,Yu Lianbo5,Ratner Lee3ORCID,Green Patrick L.16,Niewiesk Stefan16,Richner Justin M.4ORCID,Panfil Amanda R.16ORCID

Affiliation:

1. Center for Retrovirus Research, Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, Ohio, USA

2. Cellular and Molecular Biology Graduate Program, The Ohio State University, Columbus, Ohio, USA

3. Department of Medicine, Washington University, St. Louis, Missouri, USA

4. Department of Microbiology and Immunology, University of Illinois-Chicago, Chicago, Illinois, USA

5. Department of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, Ohio, USA

6. Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA

Abstract

mRNA vaccine technology has proven to be a viable approach for effectively triggering immune responses that protect against or limit viral infections and disease. In our study, we synthesized a codon optimized human T-cell leukemia virus type 1 (HTLV-1) envelope (Env) mRNA that can be delivered in a lipid nanoparticle (LNP) vaccine approach. The HTLV-1 Env mRNA-LNP produced protective immune responses against viral challenge in a preclinical rabbit model. HTLV-1 is primarily transmitted through direct cell-to-cell contact, and the protection offered by mRNA vaccines in our rabbit model could have significant implications for optimizing the development of other viral vaccine candidates. This is particularly important in addressing the challenge of enhancing protection against infections that rely on cell-to-cell transmission.

Funder

HHS | NIH | National Cancer Institute

Ohio State University

Washington University in St. Louis

Publisher

American Society for Microbiology

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