Melan-A- carrier conjugates

• US 7,537,767 B2
• Filed: 03/25/2004
• Issued: 05/26/2009
• Est. Priority Date: 03/26/2003
• Status: Expired due to Fees

• Current Assignee: Cytos Biotechnology AG (Kuros Biosciences Ltd.)
• Original Assignee: Cytos Biotechnology AG (Kuros Biosciences Ltd.)
• Inventors: Schwartz, Katrin, Bachmann, Martin F., Meijerink, Edwin, Proba, Karl G., Manolova, Vania
• Primary Examiner(s): MOSHER, MARY
• Application Number:
  US10/551,054
• Publication Number:
  US 20060204475A1
• Time in Patent Office: 1,888 Days
• Field of Search: None
• US Class Current: 424/185.1
• CPC Class Codes: A61K 2039/5258 Virus-like particles
• CPC Class Codes: A61K 2039/55561 CpG containing adjuvants; Oligonucleotide containing adjuvants
• CPC Class Codes: A61K 2039/6075 Viral proteins
• CPC Class Codes: A61K 2039/62 characterised by the link between antigen and carrier
• CPC Class Codes: A61K 2039/64 characterised by the architecture of the carrier-antigen complex, e.g. repetition of carrier-antigen units
• CPC Class Codes: A61K 39/39 characterised by the immunostimulating additives, e.g. chemical adjuvants
• CPC Class Codes: A61P 37/04 Immunostimulants
• CPC Class Codes: C07K 14/005 from viruses
• CPC Class Codes: C07K 14/4748 Tumour specific antigens; Tumour rejection antigen precursors [TRAP], e.g. MAGE
• CPC Class Codes: C12N 2710/22022 New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2730/10122 New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2730/10123 Virus like particles [VLP]
• CPC Class Codes: C12N 2760/10022 New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

The present invention is related to the fields of molecular biology, virology, immunology and medicine. The invention provides a modified virus-like particle (VLP) comprising a VLP which can be loaded with immunostimulatory substances, in particular with DNA oligonucleotides containing non-methylated C and G (CpGs), and particular peptides derived from MelanA linked thereto. Such CpGVLPs are dramatically more immunogenic than their CpG-free counterparts and induce enhanced B and T cell responses. The immune response against MelanA peptide analogues optionally coupled, fused or attached otherwise to the VLPs is similarly enhanced as the immune response against the VLP itself. In addition, the T cell responses against the MelanA peptide analogues are especially directed to the Thl type. Antigens attached to CpG-loaded VLPs may therefore be ideal vaccines for prophylactic or therapeutic vaccination against allergies, tumors and other self-molecules and chronic viral diseases.

Claims

1. A composition comprising:

(a) a virus-like particle;

(b) at least one immunostimulatory substance;

(i) wherein said immunostimulatory substance is an immunostimulatory nucleic acid; and

(ii) wherein said immunostimulatory substance is packaged into said virus-like particle; and

(c) at least one antigen or antigenic determinant;

(i) wherein said antigen or antigenic determinant is bound to said virus-like particle; and

(ii) wherein said antigen or antigenic determinant comprises a human melanoma MelanA peptide analogue that comprises an amino acid sequence derived from the amino acid sequence of SEQ ID NO;

78 or SEQ ID NO;

79 by alteration of one or two amino acid(s) or amino acid derivative(s) in said amino acid sequence, wherein said alteration comprises an amino acid substitution, deletion or insertion or a combination thereof.

2. The composition of claim 1, wherein said antigen or antigenic determinant is bound to said virus-like particle by at least one nonpeptide covalent bond.

3. The composition of claim 1, wherein said human melanoma MelanA peptide analogue is characterized by one or two amino acid substitutions with respect to the normal MelanA peptide.

4. The composition of claim 1, wherein said human melanoma MelanA peptide analogue comprises an amino acid sequence selected from the group consisting of:

(a) LAGIGILTV (SEQ ID NO;

84);

(b) MAGIGILTV (SEQ ID NO;

85);

(c) EAMGIGILTV (SEQ ID NO;

     86);

(d) ELAGIGILTV (SEQ ID NO;

     50);

(e) EMAGIGILTV (SEQ ID NO;

     87);

(f) YAAGIGILTV (SEQ ID NO;

     88); and

(g) FAAGIGILTV (SEQ ID NO;

     89).

5. The composition of claim 1, wherein said human melanoma MelanA peptide analogue comprises the sequence ELAGIGILTV (SEQ ID NO:

50).

6. The composition of claim 1, wherein said virus-like particle comprises at least one first attachment site and wherein said antigen or antigenic determinant further comprises at least one second attachment site being selected from the group consisting of:

(a) an attachment site not naturally occurring with said antigen or antigenic determinant; and

(b) an attachment site naturally occurring with said antigen or antigenic determinant;

and wherein said binding of said antigen or antigenic determinant to said virus-like particle is effected through association between said first attachment site and said second attachment site and wherein said antigen or antigenic determinant and said virus-like particle interact through said association to form an ordered and repetitive antigen array.

7. The composition of claim 6, wherein said first attachment site comprises an amino group.

8. The composition of claim 6, wherein said second attachment site comprises a sulfhydryl group.

9. The composition of claim 6, wherein said first attachment site is an amino group and said second attachment site is a sulfhydryl group.

10. The composition of claim 6, wherein said human melanoma MelanA peptide analogue with said second attachment site comprises an amino acid sequence selected from the group consisting of:

(a) CGHGHSYTTAEELAGIGILTV (SEQ ID NO;

55);

(b) CGGELAGIGILTV (SEQ ID NO;

57);

(c) CSYTTAEELAGIGILTVILGVL (SEQ ID NO;

58);

(d) CGGELAGIGILTVILGVL (SEQ ID NO;

59);

(e) ELAGIGILTVGGC (SEQ ID NO;

60);

(f) CSPKSLELAGIGILTV (SEQ ID NO;

92); and

(g) ELAGIGILTVILGVLGGC (SEQ ID NO;

93).

11. The composition of claim 6, wherein said human melanoma MelanA peptide analogue with said second attachment site comprises the amino acid sequence CGHGHSYTTAEELAGIGILTV (SEQ ID NO:

55).

12. The composition of claim 1, wherein said virus-like particle is a recombinant virus-like particle, wherein said virus like particle comprises recombinant proteins selected from the group consisting of:

(a) recombinant proteins of Hepatitis B virus;

(b) recombinant proteins of measles virus;

(c) recombinant proteins of Sindbis virus;

(d) recombinant proteins of Rotavirus;

(e) recombinant proteins of Foot-and-Mouth-Disease virus;

(f) recombinant proteins of Retrovirus;

(g) recombinant proteins of Norwalk virus;

(h) recombinant proteins of human Papilloma virus;

(i) recombinant proteins of BK virus;

(j) recombinant proteins of bacteriophages;

(k) recombinant proteins of RNA-phages;

(l) recombinant proteins of Ty; and

(m) fragments of any of the recombinant proteins from (a) to (l).

13. The composition of claim 1, wherein said virus-like particle comprises recombinant proteins, or fragments thereof, of a RNA-phage, wherein said RNA-phage is selected from the group consisting of:

(a) bacteriophage Qβ

;

(b) bacteriophage R17;

(c) bacteriophage fr;

(d) bacteriophage GA;

(e) bacteriophage SP;

(f) bacteriophage MS2;

(g) bacteriophage M11;

(h) bacteriophage MX1;

(i) bacteriophage NL95;

(j) bacteriophage f2;

(k) bacteriophage PP7; and

(l) bacteriophage AP205.

14. The composition of claim 1, wherein said virus-like particle comprises recombinant proteins, or fragments thereof, of bacteriophage Qβ

or bacteriophage AP205.

15. The composition of claim 1, wherein said immunostimulatory substance is a toll-like receptor activating substance, and wherein said immunostimulatory nucleic acid is selected from the group consisting of:

(a) ribonucleic acids;

(b) deoxyribonucleic acids;

(c) chimeric nucleic acids; and

(d) mixtures of at least one nucleic acid of (a), (b) and/or (c).

16. The composition of claim 15, wherein said deoxyribonucleic acid is an unmethylated CpG-containing oligonucleotides.

17. The composition of claim 1, wherein said immunostimulatory substance is an unmethylated CpG-containing oligonucleotide.

18. The composition of claim 17, wherein said unmethylated CpG-containing oligonucleotide comprises the sequence:

5′

X1X2CGX3X4 3′

and wherein X1, X2, X3, and X4 are any nucleotide; and

wherein at least one of said nucleotide X1, X2, X3, and X4 has a phosphate backbone modification.

19. The composition of claim 17, wherein said unmethylated CpG-containing oligonucleotide comprises a palindromic sequence.

20. The composition of claim 17, wherein said unmethylated CpG-containing oligonucleotide consists of the sequence GGGGGGGGGGGACGATCGTCGGGGGGGGGG (SEQ ID NO:

4).

21. The composition of claim 19, wherein said palindromic sequence comprises GACGATCGTC (SEQ ID NO:

1).

22. A method for enhancing an immune response against an antigen in an animal comprising introducing the composition of claim 1 into said animal, wherein an enhanced immune response against said antigen is produced in said animal.

23. The method of claim 22, wherein said immune response is an enhanced B cell response or an enhanced T cell response.

24. The method of claim 22, wherein said animal is a mammal.

25. The method of claim 22, wherein said composition is introduced into said animal subcutaneously, intramuscularly, intravenously, intranasally or directly into the lymph node.

26. An immunogenic composition comprising an immunologically effective amount of the composition of claim 1 together with a pharmaceutically acceptable diluent, carrier or excipient.

27. A method of inmmnizing or treating an animal comprising administering to said animal an immunologically effective amount of the immunogenic composition of claim 26.

28. The method of claim 27, wherein said animal is a mammal.

29. A method of immunizing or treating an animal comprising the steps of priming a T cell response in said animal, and boosting a T cell response in said animal, wherein said priming or said boosting is effected by administering an immunologically effective amount of the immunogenic composition of claim 26.

30. The method of claim 29, wherein said priming and said boosting is effected by administering an immunologically effective amount of said immunogenic composition.

31. The method of claim 23, wherein said T cell response is a CTL response or a Th cell response.

32. The method of claim 31, wherein said Th cell response is a Th1 cell response.

33. The method of claim 24, wherein said mammal is a human.

34. The immunogenic composition of claim 26, wherein said immunogenic composition further comprises an adjuvant.

35. The method of claim 28, wherein said mammal is a human.

36. The composition of claim 1, wherein said antigen or antigenic determinant consists of a human melanoma MelanA peptide analogue comprising an amino acid sequence derived from the amino acid sequence of SEQ ID NO:

78 or SEQ ID NO;

79 by alteration of one or two amino acid(s) or amino acid derivative(s) in said amino acid sequence, wherein said alteration comprises an amino acid substitution, deletion or insertion or a combination thereof.

37. The composition of claim 1, wherein said antigen or antigenic determinant consists of a human melanoma MelanA peptide analogue consisting of an amino acid sequence derived from the amino acid sequence of SEQ ID NO:

78 or SEQ ID NO;

79 by alteration of one or two amino acid(s) or amino acid derivative(s) in said amino acid sequence, wherein said alteration comprise an amino acid substitution, deletion or insertion or a combination thereof.

38. The composition of claim 1, wherein said amino acid substitution, deletion or insertion or a combination thereof is at position 1, 2, 3 or 10 of SEQ ID NO:

78 or a combination thereof or at position 1, 2 or 9 of SEQ ID NO;

79 or a combination thereof.

39. The composition of claim 1, wherein said human melanoma MelanA peptide analogue comprises an amino acid sequence derived from the amino acid sequence of SEQ ID NO:

78 or SEQ ID NO;

79 by substitution of one amino acid.

40. The composition of claim 39, wherein said substitution is at position 1, 2, 3 or 10 of SEQ ID NO:

78 or a combination thereof or at position 1, 2 or 9 of SEQ ID NO;

79 or a combination thereof.

41. The composition of claim 1, wherein said human melanoma MelanA peptide analogue consists of the sequence ELAGIGILTV (SEQ ID NO:

50).

42. The composition of claim 1, wherein said virus-like particle comprises at least one first attachment site and wherein said antigen or antigenic determinant further comprises at least one second attachment site selected from the group consisting of:

(a) an attachment site not naturally occurring with said antigen or antigenic determinant; and

(b) an attachment site naturally occurring with said antigen or antigenic determinant;

wherein said binding of said antigen or antigenic determinant to said virus-like particle is effected through association between said first attachment site and said second attachment site.

43. The composition of claim 42, wherein said antigen or antigenic determinant and said virus-like particle interact through said association to form an ordered and repetitive antigen array.

44. The composition of claim 1, wherein said virus-like particle is a virus-like particle of an RNA-phage.

45. The composition of claim 1, wherein said virus-like particle is a virus-like particle of RNA-phage Qβ

.

46. The composition of claim 1, wherein said virus-like particle comprises recombinant proteins of bacteriophage Qβ

.

47. The composition of claim 1, wherein said virus-like particle comprises recombinant proteins of bacteriophage Qβ

, wherein said recombinant proteins comprise SEQ ID NO;

10.

48. The composition of claim 1, wherein said virus-like particle comprises recombinant proteins of bacteriophage Qβ

, wherein said recombinant proteins consist of SEQ ID NO;

10.

49. The composition of claim 15, wherein said ribonucleic acids are polyinosinic-polycytidylic acid double-stranded RNA (poly-(I:

C)).

50. The composition of claim 1, wherein said immunostimulatory nucleic acid is not accessible to DNAse hydrolysis.

51. The composition of claim 45, wherein said unmethylated CpG-containing oligonucleotide consists of the sequence GGGGGGGGGGGACGATCGTCGGGGGGGGGG (SEQ ID NO:

41).

52. The composition of claim 2, wherein said virus-like particle is a virus-like particle of RNA-phage Qβ

.

53. The composition of claim 52, wherein said virus-like particle comprises recombinant proteins of bacteriophage Qβ

, and wherein said human melanoma MelanA peptide analogue consists of the sequence ELAGIGILTV (SEQ ID NO;

50).

54. The composition of claim 53, wherein said virus-like particle comprises at least one first attachment site and wherein said antigen or antigenic determinant further comprises at least one second attachment site selected from the group consisting of:

(a) an attachment site not naturally occurring with said antigen or antigenic determinant; and

(

b) an attachment site naturally occurring with said antigen or antigenic determinant;

wherein said binding of said antigen or antigenic determinant to said virus-like particle is effected through association between said first attachment site and said second attachment site, and wherein said antigen or antigenic determinant and said virus-like particle interact through said association to form an ordered and repetitive antigen array.

55. The composition of claim 54, wherein said first attachment site is an amino group and said second attachment site is a sulfhydryl group.

56. The composition of claim 55, wherein said immunostimulatory substance is an unmethylated CpG-containing oligonucleotide, and wherein said unmethylated CpG-containing oligonucleotide consists of the sequence GGGGGGGGGGGACGATCGTCGGGGGGGGGG (SEQ ID NO:

41).

57. The composition of claim 56, wherein said virus-like particle comprises recombinant proteins of bacteriophage Qβ

, wherein said recombinant proteins consist of SEQ ID NO;

10.

58. The composition of claim 57, wherein said human melanoma MelanA peptide analogue with said second attachment site consists of the amino acid sequence CGHGHSYTTAEELAGIGILTV (SEQ ID NO:

55).