Sulfated Lactosyl Archaeol Archaeosome-Adjuvanted Vaccine Formulations Targeting Rabbit Hemorrhagic Disease Virus Are Immunogenic and Efficacious

Author:

Akache Bassel1ORCID,Read Andrew J.2ORCID,Dudani Renu1,Harrison Blair A.1,Williams Dean1,Deschatelets Lise1,Jia Yimei1,Chandan Vandana1,Stark Felicity C.1,Agbayani Gerard1,Makinen Shawn R.1,Hemraz Usha D.3ORCID,Lam Edmond3ORCID,Régnier Sophie3,Zou Wei1,Kirkland Peter D.2ORCID,McCluskie Michael J.1ORCID

Affiliation:

1. National Research Council Canada, Human Health Therapeutics, Ottawa, ON K1A 0R6, Canada

2. Virology Laboratory, Elizabeth Macarthur Agricultural Institute, NSW Department of Primary Industries, Menangle, NSW 2567, Australia

3. National Research Council Canada, Aquatic and Crop Resource Development, Montreal, QC H4P 2R2, Canada

Abstract

Vaccines play an important role in maintaining human and animal health worldwide. There is continued demand for effective and safe adjuvants capable of enhancing antigen-specific responses to a target pathogen. Rabbit hemorrhagic disease virus (RHDV) is a highly contagious calicivirus that often induces high mortality rates in rabbits. Herein, we evaluated the activity of an experimental sulfated lactosyl archaeol (SLA) archaeosome adjuvant when incorporated in subunit vaccine formulations targeting RHDV. The subunit antigens consisted of RHDV–CRM197 peptide conjugates or recombinant RHDV2 VP60. SLA was able to enhance antigen-specific antibody titers and cellular responses in mice and rabbits. Three weeks following immunization, antigen-specific antibody levels in rabbits vaccinated with RHDV2 VP60 + SLA were significantly higher than those immunized with antigen alone, with geomean titers of 7393 vs. 117. In addition, the SLA-adjuvanted VP60-based formulations were highly efficacious in a rabbit RHDV2 challenge model with up to 87.5% animals surviving the viral challenge. These findings demonstrate the potential utility of SLA adjuvants in veterinary applications and highlight its activity in different types of mammalian species.

Funder

National Research Council Canada

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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