Key result
Recombinant FMDV empty capsids produced by transient gene expression in mammalian cells induced 100% protection against viral challenge in mice, matching the efficacy of the traditional inactivated vaccine.
Transient gene expression in mammalian cells is a scalable and cost-effective technology for producing a recombinant subunit vaccine against foot-and-mouth disease virus.
Foot-and-mouth disease (FMD) is a highly contagious disease of cloven-hoofed animals. It produces severe economic losses in the livestock industry. Currently available vaccines are based on inactivated FMD virus (FMDV). The use of empty capsids as a subunit vaccine has been reported to be a promising candidate because it avoids the use of virus in the vaccine production and conserves the conformational epitopes of the virus. In this report, we explored transient gene expression (TGE) in serum-free suspension-growing mammalian cells for the production of FMDV recombinant empty capsids as a subunit vaccine. The recombinant proteins produced, assembled into empty capsids and induced protective immune response against viral challenge in mice. Furthermore, they were recognized by anti-FMDV bovine sera. By using this technology, we were able to achieve expression levels that are compatible with the development of a vaccine. Thus, TGE of mammalian cells is an easy to perform, scalable and cost-effective technology for the production of a recombinant subunit vaccine against FMDV.
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Mignaqui et al. (2013) studied Foot-and-mouth disease (n=35). Recombinant FMDV empty capsids (pTT5-P12A3C) vs. Mock transfected cell lysates was evaluated on Protection against viral challenge (absence of viremia 24 h post challenge). Recombinant FMDV empty capsids produced by transient gene expression in mammalian cells induced 100% protection against viral challenge in mice, matching the efficacy of the traditional inactivated vaccine.
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