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Protein vaccines against poxviruses

a technology of poxvirus and protein, applied in the field of protein vaccines against poxviruses, can solve the problems of protein alone not conferring acceptable protection, the vaccine that eradicates pox worldwide poses serious side effects in a subset of people with acquired or congenital defects in the immune system, and the monkeypox cannot be eradicated. , to achieve the effect of increasing cross-reactivity, cross-protection, and high degree of cross-reactivity

Inactive Publication Date: 2011-04-07
HOOPER JAY W +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The protein-based vaccine regimen provides effective protection against severe monkeypox infection in non-human primates, with higher antibody titers and reduced adverse effects compared to traditional live-virus vaccines, suitable for immunocompromised individuals and offering simpler and more convenient administration.

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.

Method used

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  • Protein vaccines against poxviruses
  • Protein vaccines against poxviruses
  • Protein vaccines against poxviruses

Examples

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Embodiment Construction

[0089]In this paper is disclosed novel protein vaccines and methods of vaccination against poxviruses which contains monkeypox ortholog proteins or corresponding ortholog proteins of vaccinia or monkeypox. It is now possible to use such exogenously expressed proteins, or portions of proteins, to elicit immune responses that contribute to the protection against poxviruses in humans and other mammals. As described above, the novel protein vaccine includes at least two of the following purified recombinant monkeypox virus protein or peptide products produced by the monkeypox virus M1R, A35R, A29L and B6R open reading frames, and orthologs of these proteins or peptides having 90% amino acid identity, and an adjuvant. At least one of the peptides / proteins should be specific to an IMV immunogen (ortholog product of M1R or A29L) and at least one should be specific to an EEV immunogen (ortholog product of A35R or B6R). As noted above, preferably such orthologs are obtained from an orthopoxv...

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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...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K39/275A61K39/285A61P31/20
CPCA61K9/0019A61K39/275A61K2039/53C12N2710/24134A61K2039/555C12N2710/24034A61K2039/55561A61K39/12A61P31/12A61P31/20
Inventor HOOPER, JAY W.FRANCHINI, GENOVEFFA
Owner HOOPER JAY W
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