Vmp-like sequences of pathogenic Borrelia
US-9212218-B2 · Dec 15, 2015 · US
US9393294B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9393294-B2 |
| Application number | US-201213355468-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 20, 2012 |
| Priority date | Jan 20, 2011 |
| Publication date | Jul 19, 2016 |
| Grant date | Jul 19, 2016 |
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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.
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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
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