Use of microvirin in the identification of mycobacterium tuberculosis mannose-capped lipoarabinomannan
US-2024085416-A1 · Mar 14, 2024 · US
US9506922B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9506922-B2 |
| Application number | US-201514590810-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 6, 2015 |
| Priority date | Nov 20, 2009 |
| Publication date | Nov 29, 2016 |
| Grant date | Nov 29, 2016 |
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Methods for producing an immune response to Mycobacterium tuberculosis (Mtb) are disclosed herein. In several examples, the immune response is a protective immune response. In additional embodiments, methods are disclosed for inhibiting an infection with Mtb, preventing an infection with Mtb, or treating an infection with Mtb. Pharmaceutical compositions for the inhibition, prevention and/or treatment of tuberculosis are also disclosed.
Opening claim text (preview).
We claim: 1. A method for producing an immune response in a subject, comprising administering to the subject a therapeutically effective amount of a viral expression vector comprising a promoter operably linked to a polynucleotide encoding a polypeptide, wherein the polypeptide (a) comprises the amino acid sequence set forth as SEQ ID NO: 2; or (b) consists of contiguous amino acids 141-149 of the amino acid sequence set forth as SEQ ID NO: 2, thereby inducing an immune response to the polypeptide. 2. The method of claim 1 , wherein the polypeptide consists of amino acids 141-149 of the amino acid sequence set forth as SEQ ID NO: 2. 3. The method of claim 1 , further comprising administering a therapeutically effective amount of an adjuvant to the subject. 4. The method of claim 1 , wherein the subject is at risk for infection with Mycobacterium tuberculosis (Mtb). 5. The method of claim 1 , wherein the polypeptide consists of the amino acid sequence set forth as SEQ ID NO: 2. 6. The method of claim 1 , wherein the viral expression vector is a poxvirus vector. 7. The method of claim 6 , wherein the poxvirus vector is a vaccinia virus vector. 8. The method of claim 7 , wherein the vaccinia virus vector is a non-replicating vaccinia virus. 9. The method of claim 6 , wherein the poxvirus vector is a modified vaccinia Ankara virus. 10. The method of claim 6 , wherein the polynucleotide is operably linked to a poxviral promoter. 11. The method of claim 1 , wherein the subject is infected with Mycobacterium tuberculosis. 12. The method of claim 11 , wherein the subject has a latent infection with Mycobacterium tuberculosis. 13. A method for producing an immune response in a subject, comprising administering to the subject a therapeutically effective amount of a viral expression vector comprising a polynucleotide encoding a polypeptide, wherein the polypeptide comprises the amino acid sequence set forth as SEQ ID NO: 2, thereby inducing an immune response to the polypeptide. 14. The method of claim 13 , further comprising administering to the subject a therapeutically effective amount of an adjuvant. 15. The method of claim 13 , wherein the subject is at risk for infection with Mtb. 16. The method of claim 13 , wherein the viral expression vector is a poxvirus vector. 17. The method of claim 16 , wherein the poxvirus vector is a vaccinia virus vector. 18. The method of claim 17 , wherein the vaccinia virus vector is a non-replicating vaccinia virus. 19. The method of claim 16 , wherein the poxvirus vector is a modified vaccinia Ankara virus. 20. The method of claim 16 , wherein the polynucleotide is operably linked to a poxviral promoter. 21. The method of claim 13 , wherein the subject is infected with Mycobacterium tuberculosis. 22. The method of claim 21 , wherein the subject has a latent infection with Mycobacterium tuberculosis.
for tuberculosis · CPC title
Immunostimulants · CPC title
for influenza or rhinoviruses · CPC title
Detection of antigens from microorganism in sample from host · CPC title
Mycobacteria · CPC title
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