Filovirus Consensus Antigens, Nucleic Acid Constructs And Vaccines Made Therefrom, And Methods Of Using Same

US2020390880A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2020390880-A1
Application numberUS-202017004818-A
CountryUS
Kind codeA1
Filing dateAug 27, 2020
Priority dateApr 12, 2012
Publication dateDec 17, 2020
Grant date

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Abstract

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Nucleic acid molecules and compositions comprising one or more nucleic acid sequences that encode a consensus filovirus immunogen including a consensus Marburgvirus filovirus glycoprotein MARV GP immunogen, a consensus Ebolavirus Sudan filovirus glycoprotein SEBOV GP immunogen and a consensus Ebolavirus Zaire glycoprotein ZEBOV GP immunogen are disclosed. The coding sequences optionally include operable linked coding sequence that encode a signal peptide. Immunomodulatory methods and methods of inducing an immune response against filovirus, particularly Marburgvirus, Ebolavirus Sudan and Ebolavirus Zaire are disclosed. Method of preventing filovirus infection, particularly infection by Marburgvirus, Ebolavirus Sudan and Ebolavirus Zaire and methods of treating individuals infected with filovirus infection, particularly infection by Marburgvirus, Ebolavirus Sudan and Ebolavirus Zaire are disclosed. Consensus filovirus proteins are disclosed.

First claim

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1 . A composition comprising: a) a nucleic acid sequence that encodes a consensus Zaire ebolavirus envelope glycoprotein immunogen, the amino acid sequence of the consensus Zaire ebolavirus envelope glycoprotein immunogen selected from the group consisting of: SEQ ID NO:1 (ZEBOV CON), a fragment of SEQ ID NO:1 that comprises 600 or more amino acids, an amino acid sequence that is 95% homologous to SEQ ID NO:1, a fragment of an amino acid sequence that is 95% homologous to SEQ ID NO:1 that comprises 600 or more amino acids; SEQ ID NO:1 (ZEBOV CON) linked to an IgE signal peptide, a fragment of SEQ ID NO:1 that comprises 600 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 95% homologous to SEQ ID NO:1 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 95% homologous to SEQ ID NO:1 that comprises 600 or more amino acids linked to an IgE signal peptide; b) a nucleic acid sequence that encodes a consensus Sudan ebolavirus envelope glycoprotein immunogen, the amino acid sequence of the consensus Sudan ebolavirus envelope glycoprotein selected from the group consisting of: SEQ ID NO:2 (SUDV CON), a fragment of SEQ ID NO:2 that comprises 600 or more amino acids, an amino acid sequence that is 95% homologous to SEQ ID NO:2, a fragment of an amino acid sequence that is 95% homologous to SEQ ID NO:2 that comprises 600 or more amino acids, SEQ ID NO:2 (SUDV CON) linked to an IgE signal peptide, a fragment of SEQ ID NO:2 that comprises 600 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 95% homologous to SEQ ID NO:2 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 95% homologous to SEQ ID NO:2 that comprises 600 or more amino acids linked to an IgE signal peptide; and c) a nucleic acid sequence that encodes a Marburg marburgvirus Angola 2005 envelope glycoprotein immunogen, the amino acid sequence of the Marburg marburgvirus Angola 2005 envelope glycoprotein immunogen selected from the group consisting of: SEQ ID NO:3 (MARV), a fragment of SEQ ID NO:3 that comprises 600 or more amino acids, an amino acid sequence that is 95% homologous to SEQ ID NO:3, a fragment of an amino acid sequence that is 95% homologous to SEQ ID NO:3 that comprises 600 or more amino acids, SEQ ID NO:3 (MARV) linked to an IgE signal peptide, a fragment of SEQ ID NO:3 that comprises 600 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 95% homologous to SEQ ID NO:3 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 95% homologous to SEQ ID NO:3 that comprises 600 or more amino acids linked to an IgE signal peptide. 2 . The composition of claim 1 comprising: a first plasmid that comprises a nucleic acid sequence that encodes the consensus Zaire ebolavirus envelope glycoprotein immunogen; a second plasmid that comprises a nucleic acid sequence that encodes the consensus Sudan ebolavirus envelope glycoprotein immunogen; and a third plasmid that comprises a nucleic acid sequence that encodes the Marburg marburgvirus Angola 2005 envelope glycoprotein immunogen. 3 . The composition of claim 1 wherein: a) the amino acid sequence of the consensus Zaire ebolavirus envelope glycoprotein immunogen is selected from the group consisting of: SEQ ID NO:1 (ZEBOV CON), a fragment of SEQ ID NO:1 that comprises 630 or more amino acids, an amino acid sequence that is 98% homologous to SEQ ID NO:1, a fragment of an amino acid sequence that is 98% homologous to SEQ ID NO:1 that comprises 630 or more amino acids; SEQ ID NO:1 (ZEBOV CON) linked to an IgE signal peptide, a fragment of SEQ ID NO:1 that comprises 630 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 98% homologous to SEQ ID NO:1 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 98% homologous to SEQ ID NO:1 that comprises 630 or more amino acids linked to an IgE signal peptide; b) the amino acid sequence of the consensus Sudan ebolavirus envelope glycoprotein is selected from the group consisting of: SEQ ID NO:2 (SUDV CON), a fragment of SEQ ID NO:2 that comprises 630 or more amino acids, an amino acid sequence that is 98% homologous to SEQ ID NO:2, a fragment of an amino acid sequence that is 98% homologous to SEQ ID NO:2 that comprises 630 or more amino acids, SEQ ID NO:2 (SUDV CON) linked to an IgE signal peptide, a fragment of SEQ ID NO:2 that comprises 630 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 98% homologous to SEQ ID NO:2 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 98% homologous to SEQ ID NO:2 that comprises 630 or more amino acids linked to an IgE signal peptide; and c) the amino acid sequence of the Marburg marburgvirus Angola 2005 envelope glycoprotein immunogen is selected from the group consisting of: SEQ ID NO:3 (MARV), a fragment of SEQ ID NO:3 that comprises 635 or more amino acids, an amino acid sequence that is 98% homologous to SEQ ID NO:3, a fragment of an amino acid sequence that is 98% homologous to SEQ ID NO:3 that comprises 635 or more amino acids, SEQ ID NO:3 (MARV) linked to an IgE signal peptide, a fragment of SEQ ID NO:3 that comprises 635 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 98% homologous to SEQ ID NO:3 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 98% homologous to SEQ ID NO:3 that comprises 635 or more amino acids linked to an IgE signal peptide. 4 . The composition of claim 3 comprising: a first plasmid that comprises a nucleic acid sequence that encodes the consensus Zaire ebolavirus envelope glycoprotein immunogen; a second plasmid that comprises a nucleic acid sequence that encodes the consensus Sudan ebolavirus envelope glycoprotein immunogen; and a third plasmid that comprises a nucleic acid sequence that encodes the Marburg marburgvirus Angola 2005 envelope glycoprotein immunogen. 5 . The composition of claim 3 wherein: a) the amino acid sequence of the consensus Zaire ebolavirus envelope glycoprotein immunogen is selected from the group consisting of: SEQ ID NO:1 (ZEBOV CON), a fragment of SEQ ID NO:1 that comprises 660 or more amino acids, an amino acid sequence that is 99% homologous to SEQ ID NO:1, a fragment of an amino acid sequence that is 99% homologous to SEQ ID NO:1 that comprises 660 or more amino acids; SEQ ID NO:1 (ZEBOV CON) linked to an IgE signal peptide, a fragment of SEQ ID NO:1 that comprises 660 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 99% homologous to SEQ ID NO:1 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 99% homologous to SEQ ID NO:1 that comprises 660 or more amino acids linked to an IgE signal peptide; b) the amino acid sequence of the consensus Sudan ebolavirus envelope glycoprotein is selected from the group consisting of: SEQ ID NO:2 (SUDV CON), a fragment of SEQ ID NO:2 that comprises 660 or more amino acids, an amino acid sequence that is 99% homologous to SEQ ID NO:2, a fragment of an amino acid sequence that is 99% homologous to SEQ ID NO:2 that comprises 660 or more amino acids, SEQ ID NO:2 (SUDV CON) linked to an IgE signal peptide, a fragment of SEQ ID NO:2 that comprises 660 or more amino acids linked to an IgE signal peptide, an amino acid sequence that is 99% homologous to SEQ ID NO:2 linked to an IgE signal peptide, and a fragment of an amino acid sequence that is 99% homologous to SEQ ID NO:2 that comprises 660 or more amino acids linked to an IgE signal peptide; and c) the amino acid sequence of the Marburg marburgvirus Angola 2005 envelope glycoprotein immunogen is selected from the group consisting of: SEQ ID NO:3 (MARV), a fragment of SEQ ID NO:3 th

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Classifications

  • New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes · CPC title

  • New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes · CPC title

  • Multivalent vaccine · CPC title

  • characterised by the dose, timing or administration schedule · CPC title

  • Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title

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What does patent US2020390880A1 cover?
Nucleic acid molecules and compositions comprising one or more nucleic acid sequences that encode a consensus filovirus immunogen including a consensus Marburgvirus filovirus glycoprotein MARV GP immunogen, a consensus Ebolavirus Sudan filovirus glycoprotein SEBOV GP immunogen and a consensus Ebolavirus Zaire glycoprotein ZEBOV GP immunogen are disclosed. The coding sequences optionally include…
Who is the assignee on this patent?
Univ Pennsylvania
What technology area does this patent fall under?
Primary CPC classification A61K39/12. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Dec 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).