US5760012A
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Methods and compounds for curing diseases caused by mutations
Assignee: UNIVERSITY THOMAS JEFFERSON
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Filing: 1996-05-01
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Granted: 1998-06-02
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Expires: 2016-05-01
Abstract
Abstract The invention concerns the use of duplex oligonucleotides having both 2'-deoxyribonucleotides and ribonucleotides, wherein there is base pairing between the two types of nucleotides. The sequence of the oligonucleotide is selected so that the 3' and 5' most regions of the oligonucleotide are homologous with (identical to) the sequence of a preselected target gene of a cell. The two regions of homology embrace a region that is heterologous with the target sequence. The introduction of the oligonucleotide into the nucleus of the cell causes the alteration of the target gene such that the sequence of the altered target gene is the sequence of the heterologous region. Consequently, the oligonucleotides of the invention are termed Chimeric Repair Vectors (CRV). In one embodiment of the invention the target gene is a globin gene and the target cell is a hematopoietic stem cell. This embodiment can be used to correct certain hemoglobinopathies such as Sickle Cell Disease, β-thalassemia, and also Gaucher Disease. The rate of correction of the globin gene is high enough so that no selection of the treated hematopoietic stem cells is required to obtain a therapeutically significant effect. In one embodiment the ribose moieties of the nucleotides of the CRV contain methylated 2'-oxygens.
Inventors
- 👤 Eric B. Kmiec
- 👤 Allyson Cole-Strauss
- 👤 Kyonggeun Yoon
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 20:43
CPC Classifications
C; C12; C12N; C12N15/00; C12N15/09; C12N15/11; C12N15/113; A; A61; A61P; A61P7/00; A61P7/06; C07; C07H; C07H21/00; C07K; C07K14/00; C07K14/795; C07K14/805; C12N15/10; A61K; A61K38/00; C12N2310/00; C12N2310/10; C12N2310/13; C12N2310/30; C12N2310/32; C12N2310/321; C12N2310/50; C12N2310/53
Claims Analysis
Total Claims: 28
Claim 1
Independent Claim
136 words
A nucleic acid, having at most one 3' end and one 5' end, comprising a segment of unpaired bases disposed so that the unpaired bases separate the nucleic acid into a first strand and a second strand, which first and second strands comprise a first region and a second region, respectively, each region having at least 15 nucleotides, in which: a) each nucleotide of the first region is Watson-Crick paired to a nucleotide of the second region; b) the first region comprises at least 8 ribonucleotides having other than a 2'-hydroxyl moiety, which are Watson-Crick paired to 2'-deoxynucleotides, which ribonucleotides form at least one ribonucleotide segment of at least 3 ribonucleotides; and c) the sequence of the first or the second region is the sequence of a fragment of a wild-type allele of a human gene.
Claim 2
Dependent Claim
136 words
A nucleic acid, having at most one 3' end and one 5' end, comprising a segment of unpaired bases disposed so that the unpaired bases separate the nucleic acid into a first strand and a second strand, which first and second strands comprise a first region and a second region, respectively, each region having at least 15 nucleotides, in which: a) each nucleotide of the first region is Watson-Crick paired to a nucleotide of the second region; b) the first region comprises at least 8 ribonucleotides having other than a 2'-hydroxyl moiety, which are Watson-Crick paired to 2'-deoxynucleotides, which ribonucleotides form at least one ribonucleotide segment of at least 3 ribonucleotides; and c) the sequence of the first or the second region is the sequence of a fragment of a wild-type allele of a human gene.
Claim 3
Dependent Claim
14 words
The nucleic acid of claim 1, provided the human gene is other than ras.
Claim 4
Dependent Claim
38 words
The nucleic acid of claim 1, in which the sequence of the first or second region is 5'-AGC GCC GCC TAC GCC CAC TCG GCT GT-3' (nt 1-26 of SEQ ID NO: 88) or is a fragment thereof.
Claim 5
Dependent Claim
18 words
The nucleic acid of claim 2, provided the human gene is other than a gene encoding alkaline phosphatase.
Claim 6
Dependent Claim
53 words
The nucleic acid of claim 1, in which the first region is comprised of a first ribonucleotide segment of at least 6 contiguous ribonucleotides, a second ribonucleotide segment of at least 3 ribonucleotides, and an intervening segment disposed between the first and second ribonucleotide segments, which intervening segment comprises at least three 2'-deoxyribonucleotides.
Claim 7
Dependent Claim
19 words
The nucleic acid of claim 4, in which the second region comprises between about 20 and about 100 2'-deoxyribonucleotides.
Claim 8
Dependent Claim
37 words
The nucleic acid of claim 5, in which the first and second ribonucleotide segments each consist of between about 6 and about 13 ribonucleotides and the intervening segment consists of between about 4 and about 20 2'-deoxyribonucleotides.
Claim 9
Dependent Claim
37 words
The nucleic acid of claim 5, in which the first and second ribonucleotide segments each consist of between about 8 and about 12 ribonucleotides and the intervening segment consists of between about 4 and about 15 2'-deoxyribonucleotides.
Claim 10
Dependent Claim
29 words
The nucleic acid of claim 5, in which the first and second ribonucleotide segments each consist of about 10 ribonucleotides and the intervening segment consists of about 5 2'-deoxyribonucleotides.
Claim 11
Dependent Claim
25 words
The nucleic acid of claim 3, in which the human gene is selected from the group consisting of a β-globin gene and a glucocerebrosidase gene.
Claim 12
Dependent Claim
29 words
The nucleic acid of claim 9, in which the sequence of the first or second region is selected from the sequences of Table I or is a fragment thereof.
Claim 13
Dependent Claim
48 words
The nucleic acid of claim 9, in which the sequence of the first or second region is 5'-CAC CTG ACT CCT GAG GAG AAG TCT GCC-3' (SEQ ID NO: 99) or 5'-GAA GTT GGT GGT GAG GCC CTG GGC AGG-3' (SEQ ID NO: 100) or a fragment thereof.
Claim 14
Independent Claim
200 words
A method of repairing a mutation of a cell of a human subject, which comprises removing a cell from a subject, having a disease caused by the presence of a CRV-repairable mutation in the cell, and introducing a nucleic acid into the removed cell, wherein said nucleic acid has at most one 3' end and one 5' end and comprises a segment of unpaired bases disposed so that the unpaired bases separate the nucleic acid into a first strand and a second strand, which first and second strands comprise a first region and a second region, respectively, each region having at least 15 nucleotides, in which: a) each nucleotide of the first region is Watson-Crick paired to a nucleotide of the second region; b) the first region comprises at least 8 ribonucleotides having other than a 2'-hydroxyl moiety, which are Watson-Crick paired to 2'-deoxynucleotides, which ribonucleotides form at least one segment of at least 3 contiguous ribonucleotides; and c) the sequence of the first or the second region is the sequence of a fragment of a wild-type allele of a human gene, which fragment embraces the CRV-repairable mutation, whereby the mutation in the cell is replaced by the wild-type allele.
Claim 15
Independent Claim
200 words
A method of repairing a mutation of a cell of a human subject, which comprises removing a cell from a subject, having a disease caused by the presence of a CRV-repairable mutation in the cell, and introducing a nucleic acid into the removed cell, wherein said nucleic acid has at most one 3' end and one 5' end and comprises a segment of unpaired bases disposed so that the unpaired bases separate the nucleic acid into a first strand and a second strand, which first and second strands comprise a first region and a second region, respectively, each region having at least 15 nucleotides, in which: a) each nucleotide of the first region is Watson-Crick paired to a nucleotide of the second region; b) the first region comprises at least 8 ribonucleotides having other than a 2'-hydroxyl moiety, which are Watson-Crick paired to 2'-deoxynucleotides, which ribonucleotides form at least one segment of at least 3 contiguous ribonucleotides; and c) the sequence of the first or the second region is the sequence of a fragment of a wild-type allele of a human gene, which fragment embraces the CRV-repairable mutation, whereby the mutation in the cell is replaced by the wild-type allele.
Claim 16
Dependent Claim
37 words
The method of claim 12, in which the sequence of the first or second region is 5'-AGC GCC GCC TAC GCC CAC TCG GCT GT-3' (nt 1-26 of SEQ ID NO: 88) or is a fragment thereof.
Claim 17
Dependent Claim
18 words
The method of claim 12, which further comprises the step of reimplanting the repaired cell into the subject.
Claim 18
Dependent Claim
59 words
The method of claim 13, wherein the first region of the nucleic acid is comprised of a first ribonucleotide segment of at least 6 contiguous ribonucleotides, a second ribonucleotide segment, and an intervening segment disposed between the first and second ribonucleotide segments, which intervening segment comprises at least three 2'-deoxyribonucleotides and wherein the cell is a hematopoietic stem cell.
Claim 19
Dependent Claim
14 words
The method of claim 14, in which the intervening segment embraces the CVR-repairable mutation.
Claim 20
Dependent Claim
23 words
The method of claim 14, in which the human gene selected from the group consisting of a β-globin gene and a glucocerebrosidase gene.
Claim 21
Dependent Claim
28 words
The method of claim 16, in which the sequence of the first or second region is selected from the sequences of Table I or is a fragment thereof.
Claim 22
Dependent Claim
48 words
The method of claim 16, in which the sequence of the first or second region is 5'-CAC CTG ACT CCT GAG GAG AAG TCT GCC-3' (SEQ ID NO: 99) or 5'-GAA GTT GGT GGT GAG GCC CTG GGC AGG-3' (SEQ ID NO: 100) or is a fragment thereof.
Claim 23
Independent Claim
235 words
A method of repairing a mutation in a hepatocyte of a human subject, which comprises removing a hepatocyte from a subject, having a disease caused by the presence of a CRV-repairable mutation in the hepatocyte, and introducing a nucleic acid into the removed cell, wherein said nucleic acid has at most one 3' end and one 5' end and comprises a segment of unpaired bases disposed so that the unpaired bases separate the nucleic acid into a first strand and a second strand, which first and second strands comprise a first region and a second region, respectively, each region having at least 15 nucleotides, in which: a) each nucleotide of the first region is Watson-Crick paired to a nucleotide of the second region; b) the first region comprises at least 8 ribonucleotides having other than a 2'-hydroxyl moiety, which are Watson-Crick paired to 2'-deoxynucleotides, which ribonucleotides form a first ribonucleotide segment of at least 6 contiguous ribonucleotides, and a second ribonucleotide segment of at least 6 contiguous ribonucleotides; c) the first region further comprises an intervening segment of at least 3 deoxyribonucleotides disposed between the first and second ribonucleotide segments; and d) the sequence of the first or the second region is the sequence of a fragment of a wild-type allele of a human gene and the intervening segment embraces the CRV-repairable mutation, whereby the mutation in the cell is replaced by the wild-type allele.
Claim 24
Independent Claim
235 words
A method of repairing a mutation in a hepatocyte of a human subject, which comprises removing a hepatocyte from a subject, having a disease caused by the presence of a CRV-repairable mutation in the hepatocyte, and introducing a nucleic acid into the removed cell, wherein said nucleic acid has at most one 3' end and one 5' end and comprises a segment of unpaired bases disposed so that the unpaired bases separate the nucleic acid into a first strand and a second strand, which first and second strands comprise a first region and a second region, respectively, each region having at least 15 nucleotides, in which: a) each nucleotide of the first region is Watson-Crick paired to a nucleotide of the second region; b) the first region comprises at least 8 ribonucleotides having other than a 2'-hydroxyl moiety, which are Watson-Crick paired to 2'-deoxynucleotides, which ribonucleotides form a first ribonucleotide segment of at least 6 contiguous ribonucleotides, and a second ribonucleotide segment of at least 6 contiguous ribonucleotides; c) the first region further comprises an intervening segment of at least 3 deoxyribonucleotides disposed between the first and second ribonucleotide segments; and d) the sequence of the first or the second region is the sequence of a fragment of a wild-type allele of a human gene and the intervening segment embraces the CRV-repairable mutation, whereby the mutation in the cell is replaced by the wild-type allele.
Claim 25
Dependent Claim
16 words
The method of claim 21, wherein the nucleic acid comprises at least eight 2'-alkylether substituted ribonucleotides.
Claim 26
Dependent Claim
16 words
The method of claim 16, wherein the nucleic acid comprises at least eight 2'-alkylether substituted ribonucleotides.
Claim 27
Dependent Claim
16 words
The method of claim 13, wherein the nucleic acid comprises at least eight 2'-alkylether substituted ribonucleotides.
Claim 28
Dependent Claim
14 words
The nucleic acid of claim 5, which comprises at least eight 2'-alkylether substituted ribonucleotides.
References Cited (Backward Citations)
No citation records indexed.
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| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 2001-06-01 | 2001-12-01 | 2002-06-02 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2005-06-01 | 2005-12-01 | 2006-06-02 | $3760.00 | Window Closed / Lapsed |
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