Vaccines and compositions against Streptococcus pneumoniae

US9393294B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9393294-B2
Application numberUS-201213355468-A
CountryUS
Kind codeB2
Filing dateJan 20, 2012
Priority dateJan 20, 2011
Publication dateJul 19, 2016
Grant dateJul 19, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Streptococcus pneumoniae is a major health concern, especially in very young, elderly, or immunocompromized patients. The present disclosure provides, inter alia, certain highly effective vaccines and pharmaceutical compositions in Streptococcus pneumoniae . The antigens may be used therapeutically or prophylactically.

First claim

Opening claim text (preview).

We claim: 1. A vaccine formulation comprising: a pharmaceutically acceptable carrier; an effective amount of an adjuvant; a first isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 265, 266, or 268, or comprising the amino acid sequence of SEQ ID NO:265, 266, or 268 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; and a second isolated polypeptide comprising the amino acid sequence of SEQ ID NO:9 or 10, or comprising the amino acid sequence of SEQ ID NO:9 or 10 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 2. The vaccine formulation of claim 1 , further comprising a third isolated polypeptide comprising the amino acid sequence of SEQ ID NO:6 or 7, or comprising the amino acid sequence of SEQ ID NO:6 or 7 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 3. The vaccine formulation of claim 2 , wherein the third polypeptide consists of the amino acid sequence of SEQ ID NO:6. 4. The vaccine formulation of claim 2 , wherein the third polypeptide consists of the amino acid sequence of SEQ ID NO:7. 5. A vaccine formulation comprising: a pharmaceutically acceptable carrier; an effective amount of an adjuvant; a first isolated polypeptide comprising the amino acid sequence of SEQ ID NO:265, 266, or 268, or comprising the amino acid sequence of SEQ ID NO:265, 266, or 268 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; and a second isolated polypeptide comprising the amino acid sequence of SEQ ID NO:6 or 7, or comprising the amino acid sequence of SEQ ID NO:6 or 7 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 6. The vaccine formulation of claim 1 or 5 , wherein the first polypeptide consists of the amino acid sequence of SEQ ID NO:265. 7. The vaccine formulation of claim 1 or 5 , wherein the first polypeptide consists of the amino acid sequence of SEQ ID NO:266. 8. The vaccine formulation of claim 1 or 5 , wherein the first polypeptide consists of the amino acid sequence of SEQ ID NO:268. 9. The vaccine formulation of claim 1 , wherein the second polypeptide consists of the amino acid sequence of SEQ ID NO:9. 10. The vaccine formulation of claim 1 or 5 , wherein one or more polypeptides are conjugated to an immunogenic carrier. 11. The vaccine formulation of claim 1 or 5 , which comprises at least one lipidated polypeptide. 12. The vaccine formulation of claim 5 , wherein the second polypeptide consists of the amino acid sequence of SEQ ID NO:6. 13. The vaccine formulation of claim 5 , wherein the second polypeptide consists of the amino acid sequence of SEQ ID NO:7. 14. A vaccine formulation comprising: a pharmaceutically acceptable carrier; an effective amount of an adjuvant; a first isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 265, 266, or 268 or comprising the amino acid sequence of SEQ ID NO:265, 266, or 268 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; a second isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 6 or comprising the amino acid sequence of SEQ ID NO:6 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; and a third isolated polypeptide comprising the amino acid sequence of SEQ ID NO:7 or comprising the amino acid sequence of SEQ ID NO:7 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 15. The vaccine formulation of claim 14 , wherein the second polypeptide is lipidated. 16. The vaccine formulation of claim 14 or 15 , further comprising one or both of: a fourth isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 9 or comprising the amino acid sequence of SEQ ID NO: 9 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; and a fifth isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 10 or comprising the amino acid sequence of SEQ ID NO: 10 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 17. The vaccine formulation of claim 16 , wherein the fifth polypeptide is lipidated. 18. A vaccine formulation comprising: a pharmaceutically acceptable carrier; an effective amount of an adjuvant; a first isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 265, 266, or 268 or comprising the amino acid sequence of SEQ ID NO: 265, 266, or 268 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; a second isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 9 or comprising the amino acid sequence of SEQ ID NO: 9 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; and a third isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 10 or comprising the amino acid sequence of SEQ ID NO: 10 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 19. The vaccine formulation of claim 18 , wherein the third polypeptide is lipidated. 20. A vaccine formulation comprising: a pharmaceutically acceptable carrier; an effective amount of an adjuvant; a first isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 265 or comprising the amino acid sequence of SEQ ID NO:265 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; a second isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 6 or comprising the amino acid sequence of SEQ ID NO:6 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; a third isolated polypeptide comprising the amino acid sequence of SEQ ID NO:7 or comprising the amino acid sequence of SEQ ID NO:7 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; a fourth isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 9 or comprising the amino acid sequence of SEQ ID NO: 9 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; and a fifth isolated polypeptide comprising the amino acid sequence of SEQ ID NO: 10 or comprising the amino acid sequence of SEQ ID NO: 10 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 21. The vaccine formulation of claim 20 , wherein the adjuvant is alum. 22. The vaccine formulation of claim 20 , wherein the vaccine formulation comprises 1-1000 μg of each polypeptide. 23. The vaccine formulation of any one of claim 1 , 5 , 14 , 18 , or 20 , wherein upon administration to a subject, the vaccine formulation induces an immune response against S. pneumoniae. 24. A pharmaceutical composition comprising: a pharmaceutically acceptable carrier; an effective amount of an adjuvant; a first isolated polypeptide comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:265, 266, or 268, or comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:265, 266, or 268 lacking 1-3 amino acids from the N-terminus, C-terminus, or both; and a second isolated polypeptide comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:9 or 10, or comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:9 or 10 lacking 1-3 amino acids from the N-terminus, C-terminus, or both. 25. The pharmaceutical composition of claim 24 , further comprising a third isolated polypeptide comprising an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:6 or 7, or comprising an amino acid sequence at least 98% identical to the amino acid sequ

Assignees

Inventors

Classifications

  • A61K39/02Primary

    Bacterial antigens · CPC title

  • A61K39/092Primary

    Streptococcus · CPC title

  • characterised by the immunostimulating additives, e.g. chemical adjuvants · CPC title

  • Inorganic adjuvants · CPC title

  • Antibacterial agents · CPC title

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What does patent US9393294B2 cover?
Streptococcus pneumoniae is a major health concern, especially in very young, elderly, or immunocompromized patients. The present disclosure provides, inter alia, certain highly effective vaccines and pharmaceutical compositions in Streptococcus pneumoniae . The antigens may be used therapeutically or prophylactically.
Who is the assignee on this patent?
Gierahn Todd, Malley Richard, Genocea Biosciences Inc, and 1 more
What technology area does this patent fall under?
Primary CPC classification A61K39/02. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jul 19 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).