Recombinant listeria vaccine strains and methods of using the same in cancer immunotherapy
US-2016367650-A1 · Dec 22, 2016 · US
US10166276B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10166276-B2 |
| Application number | US-201414329092-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 11, 2014 |
| Priority date | May 2, 2006 |
| Publication date | Jan 1, 2019 |
| Grant date | Jan 1, 2019 |
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The present invention provides recombinant peptides comprising a B cell receptor (BCR) or a fragment thereof, nucleotide molecules encoding same, and vaccines and vectors comprising same; and methods of treating, inducing an immune response against, inducing a regression of, and suppressing a formation of a lymphoma, comprising administering same. The present invention also provides methods of inducing a humoral immune response in an animal against an antigen, comprising administering to the animal a fusion peptide comprising an LLO protein or fragment thereof fused to the antigen.
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What is claimed: 1. A method of inducing an immune response against a B cell lymphoma in a subject, comprising administering a pharmaceutical composition comprising a fusion polypeptide comprising a fragment of a listeriolysin O (LLO) protein and an antigen, wherein said fragment of an LLO protein is chemically conjugated to said antigen, wherein said antigen is a fragment of a B cell receptor (BCR) comprising the idiotype of said BCR, and wherein said fragment of an LLO protein is an N-terminal fragment comprising the amino acid sequence set forth in SEQ ID NO: 25 or an N-terminal LLO-detox fragment comprising the amino acid sequence set forth in SEQ ID NO: 41. 2. The method of claim 1 , wherein said fragment of a BCR is a single chain fragment of the variable regions (scFV) of said BCR. 3. The method of claim 1 , wherein said fragment of a BCR is a 38C13 idiotype of said BCR. 4. The method of claim 3 , wherein said 38C13 idiotype comprises SEQ ID NO: 48. 5. The method of claim 1 , wherein said B cell lymphoma comprises said idiotype. 6. A recombinant Listeria, comprising said fusion polypeptide of claim 1 . 7. A method of inducing an immune response against a B cell lymphoma in a subject, wherein said method comprises administering an isolated polypeptide vaccine mixture, comprising a fragment of a listeriolysin (LLO) protein and an antigen, wherein said antigen is either a. a B cell receptor (BCR); or b. a fragment of a BCR comprising the idiotype of said BCR; and wherein said fragment of an LLO protein is an N-terminal fragment comprising the amino acid sequence set forth in SEQ ID NO: 25 or an N-terminal LLO-detox fragment comprising the amino acid sequence set forth in SEQ ID NO: 41. 8. The method of claim 7 , wherein said fragment of a BCR is a single chain fragment of the variable regions (scFV) of said BCR. 9. The method of claim 7 , wherein said fragment of a BCR is a 38C13 idiotype of said BCR. 10. The method of claim 9 , wherein said 38C13 idiotype comprises SEQ ID NO: 48. 11. The method of claim 7 , wherein said B cell lymphoma comprises said idiotype. 12. The method of claim 1 , wherein said immune response treats a B cell lymphoma in said subject. 13. The method of claim 7 , wherein said immune response treats a B cell lymphoma in said subject. 14. The method of claim 1 , wherein said immune response induces the regression of a B cell lymphoma in said subject. 15. The method of claim 7 , wherein said immune response induces the regression of a B cell lymphoma in said subject. 16. The method of claim 1 , wherein said immune response overcomes immune tolerance to a B cell lymphoma in said subject. 17. The method of claim 7 , wherein said immune response overcomes immune tolerance a B cell lymphoma in said subject. 18. The method of claim 1 , wherein said immune response reduces the incidence of relapse of a B cell lymphoma in said subject. 19. The method of claim 7 , wherein said immune response reduces the incidence of relapse of a B cell lymphoma in said subject. 20. The method of claim 1 , wherein said immune response suppresses a formation of a B cell lymphoma in said subject. 21. The method of claim 7 , wherein said immune response suppresses a formation of a B cell lymphoma in said subject. 22. The method of claim 1 , wherein said immune response reduces remission of a residual B cell lymphoma disease in said subject. 23. The method of claim 7 , wherein said immune response reduces remission of a residual B cell lymphoma disease in said subject. 24. The method of claim 1 , wherein said immune response induces a humoral response against a B cell lymphoma in said subject. 25. The method of claim 1 , further comprising inducing an antiserum. 26. A method of producing a monoclonal antibody, comprising inducing a humoral immune response in an animal according to the method of claim 1 . 27. The method of claim 7 , wherein said immune response induces humoral response against a B cell lymphoma in said subject. 28. The method of claim 7 , further comprising inducing an antiserum. 29. A method of producing a monoclonal antibody, comprising inducing a humoral immune response in an animal according to the method of claim 7 .
from Corynebacterium (G) · CPC title
against an idiotypic determinant on Ig · CPC title
from bacteria · CPC title
Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies · CPC title
Immunoglobulin superfamily · CPC title
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