Protein vaccines against poxviruses

Abstract

The invention described here entails a protein vaccine against poxviruses which contains at least two purified recombinant monkeypox virus proteins or peptides. The proteins or peptides are encoded by the open reading frames of the monkeypox ortholog genes M1R, A35R, A29L B6R, and orthologs of these proteins or peptides having 90% identity. The invention also entails a vaccine protocol against poxvirus whereby a vaccine is vaccinated with a first vaccine made up of a nucleic acid vaccine of three or more poxvirus virus genes, and subsequently vaccinated with at least one other booster vaccine made up of two or more poxvirus virus proteins.

Description

[0001]This application claims the benefit of priority from provisional application No. 60 / 722,082, filed Sep. 21, 2005, and is a divisional application of application Ser. No. 11 / 523,867, filed Sep. 20, 2006, and the entire contents of these applications are incorporated herein by reference.[0002]Viruses in the family Poxyiridae, including vaccinia virus (VACV), variola virus (smallpox), and monkeybox virus, are characterized by a large linear double-stranded DNA genome (130-300 kb) packaged in a relatively large virion (.about.350.times.270 nm), and a cytoplasmic site of replication (reviewed by Moss, 1996, In “Fields Virology”, D. M. Knipe et al. Eds., vol. 3, pp 2637-2671. Lippincott-Raven, Philadelphia). Assembly of VACV virions begins with condensation of dense granular material into membrane-wrapped particles called intracellular mature virions (IMV). Recent findings indicate the IMV are wrapped by a single membrane (Hollingshead et al., 1999, J. Virol. 73, 1503-1517) rather t...

AI Technical Summary

Benefits of technology

[0017]Thus, what is described here, in one embodiment, is a protein-based replacement vaccine and vaccination methodology to effectively protect against variola virus (smallpox), monkeypox virus, other poxviruses having 90% amino acid identity, and engineered poxviruses without any of the drawbacks associated with live-virus vaccines. This is especially relevant to immunocompromised persons who cannot be vaccinated with live vaccinia virus. It also represents an improvement over DNA vaccines alone, in terms of being simpler and more convenient, and often more effective.

[0031]Together with the protein vaccine, this invention contemplates other protein vaccines especially when used in conjunction with DNA vaccines. It is known that vaccination with DNA vaccines using vaccinia genes will achieve a response of cross-reaction and cross-protection against another poxvirus. Similar results were found regarding cross-reactivity using a DNA vaccine of monkeypox genes or a vaccine of monkeypox proteins, for instance in vaccinia plaque reduction neutralization tests and EEV spread inhibition assays. Since there is a high degree of cross-reactivity between vaccinia and monkeypox for all of the above-described four proteins / gene products, orthologs (especially from the variola virus which is extremely similar in sequence) having more than 90% identity will also cause immunogenic reactions in each other—and of course the orthologs will be best suited for causing immunogenic reactions in the respective poxvirus from which they are derived. Furthermore, it is preferred that the vaccines and immunogenic compositions described herein—whether DNA vaccine or protein vaccine / immunogenic composition—contain redundant IMV and EEV targets since this will increase cross-reactivity and cross-protection. Having such redundancy will provide enough or more than enough cross-reactive epitopes so as to afford vaccine protection—that is, because the proteins are so similar, the redundant nature of a DNA or protein vaccine containing three or four of the genes / gene products compensates for the possibility that the antibody to one protein won't cross-react with a particular virus. Hence, it is most preferred that the vaccines and immunogenic compositions contain all four of the genes / gene products L1R, A27L, A33R and B5R, or monkeypox orthologs, M1R, A29L, A35R and B6R, or other poxvirus orthologs / ortholog products.

Problems solved by technology

However, in contrast to smallpox, monkeypox cannot be eradicated.

The live vaccine (Dryvax) that has eradicated smallpox worldwide poses serious side effects in a subset of people with acquired or congenital defects in the immune system.

Interestingly, DNA alone when delivered by needle injection, or proteins alone did not confer acceptable protection, whereas the combination of DNA and proteins did.

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