Composition for introducing nucleic acid complexes into higher eucaryotic cells

• US 5,547,932 A
• Filed: 09/23/1992
• Issued: 08/20/1996
• Est. Priority Date: 09/30/1991
• Status: Expired due to Term

• Current Assignee: Boehringer Ingelheim International GmbH (C.H. Boehringer Sohn AG & Co. KG), Genentech, Inc. (Roche Holding AG), University of North Carolina At Chapel Hill (University of North Carolina System)
• Original Assignee: Boehringer Ingelheim International GmbH (C.H. Boehringer Sohn AG & Co. KG), Genentech, Inc. (Roche Holding AG)
• Inventors: Zatloukal, Kurt, Cotten, Matthew, Wagner, Ernst, Plank, Christian, Curiel, David T., Oberhauser, Berndt, Birnstiel, Max L., Schmidt, Walter G. M.
• Primary Examiner(s): Jones, W. Gary
• Assistant Examiner(s): Sisson, Bradley L.
• Application Number:
  US07/948,357
• Time in Patent Office: 1,427 Days
• Field of Search: 435/6, 435/91.1, 435/7.2, 435/7.21, 435/7.23, 435/7.24, 435/69.1, 435/172.1, 435/172.3, 435/267, 435/5, 435/91.4, 435/91.41, 435/240.2, 435/252.3, 536/23.1, 536/23.4, 536/23.5-.51, 536/24.5, 930/220, 930/221, 935/22-24, 935/59, 935/60, 935/62, 935/76, 935/32, 935/57, 935/71, 935/63
• US Class Current: 435/456
• CPC Class Codes: A61K 38/00 Medicinal preparations containing peptides peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00
• CPC Class Codes: A61K 47/50 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
• CPC Class Codes: A61K 47/6901 Conjugates being cells, cell fragments, viruses, ghosts, red blood cells or viral vectors
• CPC Class Codes: A61K 48/00 Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
• CPC Class Codes: A61P 31/12 Antivirals
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: C07K 14/005 from viruses
• CPC Class Codes: C07K 14/56 IFN-alpha
• CPC Class Codes: C07K 14/775 Apolipopeptides
• CPC Class Codes: C07K 14/79 Transferrins, e.g. lactoferrins, ovotransferrins
• CPC Class Codes: C07K 16/00 Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies antibodies with enzymatic activity, e.g. abzymes C12N9/0002
• CPC Class Codes: C07K 16/2803 against the immunoglobulin superfamily
• CPC Class Codes: C07K 2317/77 Internalization into the cell
• CPC Class Codes: C07K 2319/00 Fusion polypeptide
• CPC Class Codes: C12N 15/87 Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
• CPC Class Codes: C12N 2710/10251 Methods of production or purification of viral material
• CPC Class Codes: C12N 2710/10261 Methods of inactivation or attenuation
• CPC Class Codes: C12N 2710/10322 New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2710/10351 Methods of production or purification of viral material
• CPC Class Codes: C12N 2710/10361 Methods of inactivation or attenuation
• CPC Class Codes: C12N 2710/10363 : by chemical treatment
• CPC Class Codes: C12N 2740/11022 : New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2740/15022 : New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2740/16022 : New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2740/16122 : New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2760/16122 : New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2770/32722 : New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
• CPC Class Codes: C12N 2770/32761 : Methods of inactivation or attenuation
• CPC Class Codes: C12N 7/00 : Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof preparing medicinal viral antigen or antibody compositions, e.g. virus vaccines, A61K39/00
• CPC Class Codes: Y10T 436/143333 : Saccharide [e.g., DNA, etc.]

Abstract

A composition for the transfection of higher eucaryotic cells, comprising complexes of nucleic acid, a substance having an affinity for nucleic acid and optionally an internalizing factor, contains an endosomolytic agent, e.g. a virus or virus component, which may be conjugated. The endosomolytic agent, which is optionally part of the nucleic acid complex, is internalized into the cells together with the complex and releases the contents of the endosomes into the cytoplasm, thereby increasing the gene transfer capacity. Pharmaceutical preparations, transfection kits and methods for introducing nucleic acid into higher eucaryotic cells by treating the cells with the composition are also disclosed.

Claims

1. A process for introducing nucleic acid into the cytoplasm of a higher eucaryotic cell, which comprises contacting the cell with a composition of matter which comprises a complex, wherein said complex comprises

(a) a nucleic acid of interest,

(b) a substance having affinity for nucleic acid, and

(c) an endosomolytic agent, whereby said complex is internalized into the cell by endocytosis, and is released into the cytoplasm of said cell by endosomolysis.

2. A process according to claim 1, characterized in that the cell is a human cell.

3. A process according to claim 2, characterized in that the cell is a human tumor cell.

4. A process according to claim 3, further characterized in that tumor cells are contacted with the composition of matter ex vivo and that said nucleic acid encodes one or more immune modulating substances.

5. A process according to claim 4, characterized in that the one or more immune modulating substances are cytokines.

6. A process according to claim 5, characterized in that said DNA encodes Interleukin-2.

7. A process according to claim 3, further characterized in that tumor cells are contacted with the composition of matter ex vivo and that said DNA encodes one or more immune modulating substances.

8. A process according to claim 7, characterized in that the one or more immune modulating substances are cytokines.

9. A process according to claim 2, characterized in that the cell is a human myoblast.

10. A process according to claim 2, characterized in that the cell is a human fibroblast.

11. A process according to claim 2, characterized in that the cell is a human hepatocyte.

12. A process according to claim 2, characterized in that the cell is a human endothelial cell.

13. A process according to claim 2, characterized in that the cell is a human lung epithelial cell.

14. A process according to claim 2, characterized in that the nucleic acid is DNA active in gene therapy.

15. A process according to claim 14, characterized in that said DNA encodes factor VIII.

16. A process according to claim 1, characterized in that the endosomolytic agent is bound to a substance having affinity for nucleic acid and has the ability of being internalized into said cells as a component of the complex.

17. A process according to claim 16, characterized in that the endosomolytic agent is covalently bound to a substance having affinity for nucleic acid.

18. A process according to claim 16, characterized in that the endosomolytic agent is non-covalently bound to a substance having affinity for nucleic acid.

19. A process according to claim 18, characterized in that the binding is effected via a biotin-streptavidin bridge.

20. A process according to claim 18, characterized in that the binding is effected ionically.

21. A process according to claim 16, characterized in that the endosomolytic agent is bound to the nucleic acid directly via said substance having affinity for nucleic acid.

22. A process according to claim 16, characterized in that the endosomolytic agent is a virus or a virus component.

23. A process according to claim 2 or 16, characterized in that the cell is a bone marrow cell.

24. A process according to claim 1 or 16, characterized in that the endosomolytic agent is a virus or a virus component which is an internalizing factor per se for said cells.

25. A process according to claim 22, characterized in that the virus is an adenovirus.

26. A process according to claim 25, characterized in that the adenovirus is a mutant.

27. A process according to claim 26, characterized in that the adenovirus is a replication-incompetent mutant.

28. A process according to claim 27, characterized in that the adenovirus has one or more mutations or deletions in the E1A region.

29. A process according to claim 25, characterized in that the adenovirus is inactivated.

30. A process according to claim 29, characterized in that the adenovirus is inactivated by short wave UV.

31. A process according to claim 29, characterized in that the adenovirus is inactivated by UV/psoralen.

32. A process according to claim 29, characterized in that the adenovirus is inactivated by formaldehyde.

33. A process according to claim 22, characterized in that the virus component is one or more adenovirus proteins.

34. A process according to claim 22, characterized in that the virus or virus component is a picornavirus and the process is carried out in vitro or ex vivo.

35. A process according to claim 34, characterized in that said picornavirus is a rhinovirus.

36. A process according to claim 35, characterized in that the rhinovirus is inactivated.

37. A process according to claim 16, characterized in that the endosomolytic agent is an endosomolytic peptide.

38. A process according to claim 37, characterized in that the endosomolytic peptide is a viral peptide.

39. A process according to claim 38, characterized in that the viral peptide is modified.

40. A process according to claim 39, characterized in that the endosomolytic viral peptide contains a nucleic acid binding domain.

41. A process according to claim 38, characterized in that the endosomolytic viral peptide is an influenza-hemagglutinin HA2 peptide.

42. A process according to claim 41, characterized in that the peptide has the sequence identified as SEQ ID NO:

1.

43. A process according to claim 41, characterized in that the peptide has the sequence identified as SEQ ID NO:

2.

44. A process as claimed in claim 16, characterized in that the nucleic acid is DNA active in gene therapy.

45. A process as claimed in claim 44, characterized in that said DNA encodes factor VIII.

46. A process as claimed in claim 44, characterized in that a tumor cell is contacted with the composition of matter ex vivo and that said DNA encodes one or more immune modulating substances.

47. A process as claimed in claim 46, wherein said one or more immune modulating substances are cytokines.

48. A process as claimed in claim 47, wherein said cytokine is Interleukin-2.

49. A process according to claim 16, characterized in that said cell is a human cell.

50. A process according to claim 49, characterized in that said cell is a human tumor cell.

51. A process as claimed in claim 50, characterized in that the tumor cell is contacted with the composition of matter ex vivo and that said DNA encodes one or more immune modulating substances.

52. A process as claimed in claim 51, wherein said one or more immune modulating substances are cytokines.

53. A process according to claim 49, characterized in that said cell is a human myoblast.

54. A process as claimed in claim 49, wherein said cell is a human fibroblast.

55. A process as claimed in claim 49, wherein said cell is a human hepatocyte.

56. A process as claimed in claim 49, wherein said cell is a human endothelial cell.

57. A process as claimed in claim 49, wherein said cell is a human lung epithelial cell.

58. A process as claimed in claim 1, characterized in that said complex further comprises an internalizing factor for the cells.

59. A process according to claim 1, characterized in that the endosomolytic agent is a virus or a virus component.

60. A process according to claim 1, wherein said endosomolytic agent comprises an endosomolytic peptide coupled with the substance having affinity for nucleic acid;

wherein said endosomolytic agent has the ability of being internalized into said cells as a component of the complex.

61. A process as claimed in claim 60, characterized in that said complex further comprises an internalizing factor for the cells.

62. A process according to claim 61, characterized in that the endosomolytic agent is a virus component.

63. A process according to claim 60, characterized in that the endosomolytic agent is a virus component.

64. A process according to claim 39 or 37, characterized in that the peptide has a nucleic acid binding domain.

65. A process according to claim 64, characterized in that said internalizing factor is bound to a substance having affinity for nucleic acid.

66. A process according to claim 58 or 65, characterized in that the internalizing factor is a ligand for hepatocytes.

67. A process according to claim 66, characterized in that the internalizing factor is a ligand for the asialoglycoprotein receptor.

68. A process according to claim 66, characterized in that the internalizing factor is a tetra-galactose-polylysine.

69. A process according to claim 58 or 65, characterized in that the internalizing factor is transferrin.

70. A process according to claim 58 or 65, characterized in that the internalizing factor is a low density lipoprotein.

71. A process according to claim 64 or 65, characterized in that the endosomolytic agent is a virus or a virus component which is not an internalizing factor for a human cell.

72. A process according to claim 71, characterized in that the virus or virus component is a virus which is infectious for a species other than human.

73. A process according to claim 72, characterized in that the virus is an adenovirus.

74. A process according to claim 73, characterized in that the adenovirus is avian.

75. A process according to claim 74, characterized in that the adenovirus is the Chick Embryo Lethal Orphan virus.