US2010330037A1PendingUtilityA1
Adenoviral systems and the uses thereof
Est. expiryDec 28, 2020(expired)· nominal 20-yr term from priority
Inventors:Per Holm
A61P 35/00A61P 43/00A61K 38/00A61K 48/00C07K 14/4702C12N 2830/008C12N 15/86C12N 2710/10343
59
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Claims
Abstract
The invention is related to a nucleic acid comprising an adenoviral nucleic acid, which also comprises a nucleic acid sequence coding for YB-1.
Claims
exact text as granted — not AI-modified1 - 46 . (canceled)
47 . A nucleic acid comprising an adenoviral nucleic acid, characterized in that the nucleic acid comprises a nucleic acid sequence coding for YB-1.
48 . The nucleic acid of claim 47 , characterized in that the adenoviral nucleic acid comprises a nucleic acid coding for E1-B.
49 . The nucleic acid of claim 48 , characterized in that the adenoviral nucleic acid comprises a nucleic acid coding for E4orf6.
50 . The nucleic acid of claim 48 , characterized in that a promoter is provided which controls the expression of E1-B.
51 . The nucleic acid of claim 49 , characterized in that a promoter is provided which controls the expression of E4orf6.
52 . The nucleic acid of claim 48 , characterized in that E1B is the E1-B 55 kDa protein.
53 . The nucleic acid of the claim 48 , characterized in that the nucleic acid codes for functionally inactive gene products E1 B and/or E1 and/or E3 and/or E4.
54 . A nucleic acid comprising a nucleic acid coding for YB-1 and a nucleic acid sequence mediating a nuclear transport of YB-1.
55 . The nucleic acid of claim 54 , characterized in that the nucleic acid sequence mediating the nuclear transport of YB-1 is selected from the group comprising signal sequences and transport sequences.
56 . A nucleic acid comprising an adenoviral nucleic acid, characterized in that the adenoviral nucleic acid comprises a tumour-specific promoter instead of a functional E2 late promoter.
57 . A nucleic acid comprising an adenoviral nucleic acid, characterized in that the adenoviral nucleic acid comprises a tissue-specific promoter instead of a functional E2 late promoter.
58 . The nucleic acid of claim 57 , characterized in that the adenoviral nucleic acid contains a non-functional E2 early promoter.
59 . An adenoviral replication system comprising an adenoviral nucleic acid, whereby the adenoviral nucleic acid is deficient for the expression of the E1A protein, and comprising a nucleic acid of a helper virus, whereby the nucleic acid of the helper virus comprises a nucleic acid sequence which codes for YB-1.
60 . The adenoviral replication system of claim 59 , characterized in that the adenoviral nucleic acid and/or the nucleic acid of the helper virus is present as a replicable vector.
61 . A vector, preferably an expression vector, comprising a nucleic acid of claim 47 , 54 , 56 or 57 .
62 . A group of vectors comprising of at least two vectors, whereby the overall group of vectors contains an adenoviral replication system of claim 60 .
63 . The group of vectors of claim 62 , characterized in that each component of the adenoviral replication system is located on a suitable vector, preferably an expression vector.
64 . The group of vectors of claim 62 , characterized in that at least two components of the adenoviral replication system are located on a vector of the group of vectors.
65 . An adenovirus comprising a nucleic acid of claim 47 , 54 , 56 or 57 .
66 . The adenovirus of claim 65 comprising a capsid.
67 . A cell comprising a nucleic acid of claim 47 , 54 , 56 or 57 and/or an adenoviral replication system of claim 60 and/or a vector of claim 61 and/or a group of vectors of claim 62 and/or an adenovirus of claim 65 .
68 . Use of a nucleic acid of claim 47 , 54 , 56 or 57 and/or an adenoviral replication system of claim 60 and/or a vector of claim 61 and/or a group of vectors of claim 62 and/or an adenovirus of claim 65 and/or a cell claim 67 for the manufacture of a medicament.
69 . The use of claim 68 , characterized in that the medicament is used for the treatment and/or prophylaxis of tumour diseases.
70 . The use of claim 68 , characterized in that the medicament additionally contains a pharmaceutically effective compound.
71 . The use of claim 70 , characterized in that the pharmaceutically effective compound is selected from the group comprising cytostatic agents, whereby the cytostatic agents are preferably selected from the group comprising cis-platinum, Taxol, Daunoblastin, Adriamycin and Mitoxantron.
72 . Use of a nucleic acid of claim 47 , 54 , 56 or 57 and/or an adenoviral replication system of claim 60 and/or a vector of claim 58 and/or a group of vectors of claim 62 and/or an adenovirus of claim 65 and/or a cell of claim 67 for the manufacture of a medicament for the treatment and/or prophylaxis of tumour diseases, whereby YB-1 is located in the nucleus of the tumour cells independent of the cell cycle.
73 . The use of claim 72 , characterized in that the nucleic acid codes for an adenoviral nucleic acid and that the adenoviral nucleic acid is E1B-deficient, and in particular E1B 55 kDa-deficient.
74 . The use of claim 72 , characterized in that the adenovirus is E1B-deficient, and in particular E1B 55 kDa-deficient.
75 . The use of claim 72 , characterized in that the nucleic acid codes for an adenoviral nucleic acid and that the adenoviral nucleic acid codes for E1B, and codes in particular for E1B 55 kDa.
76 . The use of claim 72 , characterized in that the adenovirus expresses E1B, and expresses in particular E1B 55 kDa.
77 . The use of claims 72 , characterized in that the adenoviral nucleic acid codes for E1 A.
78 . The use of claims 72 , characterized in that the adenovirus expresses E1A.
79 . The use of claim 76 , characterized in that the tumour and/or the tumour disease is selected from the group comprising p53-positive tumours, p53-negative tumours, malignant tumours, benign tumours and combinations thereof.
80 . A method for the screening of patients who can be treated with an E1B-deficient, preferably E1B 55 kDa-deficient adenovirus characterized by the following steps:
examining a sample of the tumour tissue and determining whether YB-1 is located in the nucleus independently of the cell cycle.
81 . The method of claim 80 , characterized in that the tumour tissue is examined using antibodies against YB-1.Join the waitlist — get patent alerts
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