EA005157B1 - Методы и составы для лечения сердечной недостаточности и вентрикулярной коррекции путем доставки in vivo ангиогенных трансгенов - Google Patents
Методы и составы для лечения сердечной недостаточности и вентрикулярной коррекции путем доставки in vivo ангиогенных трансгенов Download PDFInfo
- Publication number
- EA005157B1 EA005157B1 EA199901002A EA199901002A EA005157B1 EA 005157 B1 EA005157 B1 EA 005157B1 EA 199901002 A EA199901002 A EA 199901002A EA 199901002 A EA199901002 A EA 199901002A EA 005157 B1 EA005157 B1 EA 005157B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- vector
- angiogenic protein
- peptide
- promoter
- fgf
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 213
- 206010019280 Heart failures Diseases 0.000 title claims abstract description 96
- 208000033774 Ventricular Remodeling Diseases 0.000 title abstract 3
- 108700019146 Transgenes Proteins 0.000 title description 76
- 230000002491 angiogenic effect Effects 0.000 title description 36
- 239000000203 mixture Substances 0.000 title description 14
- 238000001727 in vivo Methods 0.000 title 1
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 293
- 239000013598 vector Substances 0.000 claims abstract description 209
- 108010074415 Angiogenic Proteins Proteins 0.000 claims abstract description 176
- 102000008076 Angiogenic Proteins Human genes 0.000 claims abstract description 174
- 230000017531 blood circulation Effects 0.000 claims abstract description 116
- 210000002216 heart Anatomy 0.000 claims abstract description 88
- 239000007924 injection Substances 0.000 claims abstract description 87
- 238000002347 injection Methods 0.000 claims abstract description 87
- 241000701161 unidentified adenovirus Species 0.000 claims abstract description 81
- 230000014509 gene expression Effects 0.000 claims abstract description 69
- 230000002107 myocardial effect Effects 0.000 claims abstract description 62
- 210000004351 coronary vessel Anatomy 0.000 claims abstract description 61
- 210000004165 myocardium Anatomy 0.000 claims abstract description 61
- 230000003612 virological effect Effects 0.000 claims abstract description 50
- 239000002245 particle Substances 0.000 claims abstract description 46
- 208000010125 myocardial infarction Diseases 0.000 claims abstract description 38
- 239000013603 viral vector Substances 0.000 claims abstract description 36
- 108010076504 Protein Sorting Signals Proteins 0.000 claims abstract description 35
- 210000004204 blood vessel Anatomy 0.000 claims abstract description 33
- 206010007559 Cardiac failure congestive Diseases 0.000 claims abstract description 27
- 210000004413 cardiac myocyte Anatomy 0.000 claims abstract description 23
- 210000004369 blood Anatomy 0.000 claims abstract description 22
- 239000008280 blood Substances 0.000 claims abstract description 22
- 150000002632 lipids Chemical class 0.000 claims abstract description 15
- 208000031225 myocardial ischemia Diseases 0.000 claims abstract description 15
- 210000001567 regular cardiac muscle cell of ventricle Anatomy 0.000 claims abstract description 13
- 201000010046 Dilated cardiomyopathy Diseases 0.000 claims abstract description 12
- 108090000723 Insulin-Like Growth Factor I Proteins 0.000 claims abstract description 11
- 102000013275 Somatomedins Human genes 0.000 claims abstract description 11
- 108010073929 Vascular Endothelial Growth Factor A Proteins 0.000 claims abstract description 11
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 claims abstract description 11
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 claims abstract description 11
- 206010056370 Congestive cardiomyopathy Diseases 0.000 claims abstract description 10
- 102000018233 Fibroblast Growth Factor Human genes 0.000 claims abstract description 10
- 108050007372 Fibroblast Growth Factor Proteins 0.000 claims abstract description 10
- 210000003752 saphenous vein Anatomy 0.000 claims abstract description 10
- 102000005604 Myosin Heavy Chains Human genes 0.000 claims abstract description 9
- 229940126864 fibroblast growth factor Drugs 0.000 claims abstract description 9
- 241000702421 Dependoparvovirus Species 0.000 claims abstract description 6
- 101000629029 Homo sapiens Myosin regulatory light chain 2, ventricular/cardiac muscle isoform Proteins 0.000 claims abstract description 6
- 102100026925 Myosin regulatory light chain 2, ventricular/cardiac muscle isoform Human genes 0.000 claims abstract description 6
- 108010051583 Ventricular Myosins Proteins 0.000 claims abstract 4
- 230000002861 ventricular Effects 0.000 claims description 88
- 238000012937 correction Methods 0.000 claims description 36
- 210000001519 tissue Anatomy 0.000 claims description 31
- 230000010076 replication Effects 0.000 claims description 28
- 210000001367 artery Anatomy 0.000 claims description 19
- 230000002950 deficient Effects 0.000 claims description 17
- 101100296652 Caenorhabditis elegans pcp-5 gene Proteins 0.000 claims description 15
- 102100028516 Receptor-type tyrosine-protein phosphatase U Human genes 0.000 claims description 13
- 101710138774 Receptor-type tyrosine-protein phosphatase U Proteins 0.000 claims description 13
- 230000003248 secreting effect Effects 0.000 claims description 12
- 239000003102 growth factor Substances 0.000 claims description 7
- 230000002708 enhancing effect Effects 0.000 claims description 6
- 210000005075 mammary gland Anatomy 0.000 claims description 4
- -1 PCP-6 Proteins 0.000 claims description 3
- 230000009528 severe injury Effects 0.000 claims description 3
- 102100035475 Blood vessel epicardial substance Human genes 0.000 claims 1
- 101100135798 Caenorhabditis elegans pcp-1 gene Proteins 0.000 claims 1
- 101100351213 Chromobacterium violaceum (strain ATCC 12472 / DSM 30191 / JCM 1249 / NBRC 12614 / NCIMB 9131 / NCTC 9757) pcp gene Proteins 0.000 claims 1
- 101001094636 Homo sapiens Blood vessel epicardial substance Proteins 0.000 claims 1
- 101000608194 Homo sapiens Pyrin domain-containing protein 1 Proteins 0.000 claims 1
- 101000595404 Homo sapiens Ribonucleases P/MRP protein subunit POP1 Proteins 0.000 claims 1
- 101100126615 Mus musculus Itpr1 gene Proteins 0.000 claims 1
- 101150025129 POP1 gene Proteins 0.000 claims 1
- WPBUPFBTCDYKNM-UHFFFAOYSA-M [6-(diethylamino)-9-(2-octadecoxycarbonylphenyl)xanthen-3-ylidene]-diethylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CCCCCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C1=C2C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C21 WPBUPFBTCDYKNM-UHFFFAOYSA-M 0.000 claims 1
- 101150075058 pcp1 gene Proteins 0.000 claims 1
- 241000700605 Viruses Species 0.000 abstract description 59
- 230000001965 increasing effect Effects 0.000 abstract description 28
- 230000028327 secretion Effects 0.000 abstract description 14
- 208000029078 coronary artery disease Diseases 0.000 abstract description 12
- 210000001349 mammary artery Anatomy 0.000 abstract description 6
- 108090000379 Fibroblast growth factor 2 Proteins 0.000 abstract 6
- 102000003974 Fibroblast growth factor 2 Human genes 0.000 abstract 6
- 108090000386 Fibroblast Growth Factor 1 Proteins 0.000 abstract 4
- 102000003971 Fibroblast Growth Factor 1 Human genes 0.000 abstract 4
- 108090000381 Fibroblast growth factor 4 Proteins 0.000 abstract 4
- 102100028072 Fibroblast growth factor 4 Human genes 0.000 abstract 4
- 108090000380 Fibroblast growth factor 5 Proteins 0.000 abstract 4
- 102100028073 Fibroblast growth factor 5 Human genes 0.000 abstract 4
- 108010038512 Platelet-Derived Growth Factor Proteins 0.000 abstract 4
- 102000010780 Platelet-Derived Growth Factor Human genes 0.000 abstract 4
- 108090000382 Fibroblast growth factor 6 Proteins 0.000 abstract 2
- 102100028075 Fibroblast growth factor 6 Human genes 0.000 abstract 2
- 101000808011 Homo sapiens Vascular endothelial growth factor A Proteins 0.000 abstract 2
- 102100037596 Platelet-derived growth factor subunit A Human genes 0.000 abstract 2
- 102000009520 Vascular Endothelial Growth Factor C Human genes 0.000 abstract 2
- 108010073923 Vascular Endothelial Growth Factor C Proteins 0.000 abstract 2
- 102000058223 human VEGFA Human genes 0.000 abstract 2
- 108010017843 platelet-derived growth factor A Proteins 0.000 abstract 2
- 230000002939 deleterious effect Effects 0.000 abstract 1
- 238000012546 transfer Methods 0.000 description 127
- 241001465754 Metazoa Species 0.000 description 108
- 210000004027 cell Anatomy 0.000 description 108
- 230000000638 stimulation Effects 0.000 description 93
- 230000006870 function Effects 0.000 description 51
- 102000004169 proteins and genes Human genes 0.000 description 51
- 230000033115 angiogenesis Effects 0.000 description 39
- 230000000302 ischemic effect Effects 0.000 description 39
- 108091033319 polynucleotide Proteins 0.000 description 39
- 102000040430 polynucleotide Human genes 0.000 description 39
- 239000002157 polynucleotide Substances 0.000 description 39
- 230000000694 effects Effects 0.000 description 35
- 239000013612 plasmid Substances 0.000 description 31
- 230000008719 thickening Effects 0.000 description 30
- 230000002792 vascular Effects 0.000 description 30
- 238000005259 measurement Methods 0.000 description 28
- 108010016628 ameroid Proteins 0.000 description 26
- 230000008602 contraction Effects 0.000 description 24
- 238000011282 treatment Methods 0.000 description 24
- 108020004414 DNA Proteins 0.000 description 23
- 210000001736 capillary Anatomy 0.000 description 23
- 208000024891 symptom Diseases 0.000 description 22
- 102100029112 Endothelin-converting enzyme 1 Human genes 0.000 description 19
- 230000010412 perfusion Effects 0.000 description 18
- 108091026890 Coding region Proteins 0.000 description 17
- 101000841259 Homo sapiens Endothelin-converting enzyme 1 Proteins 0.000 description 17
- 101000967022 Locusta migratoria Endothelin-converting enzyme homolog Proteins 0.000 description 17
- 230000000747 cardiac effect Effects 0.000 description 17
- 108090000765 processed proteins & peptides Proteins 0.000 description 17
- 239000012634 fragment Substances 0.000 description 16
- 238000001415 gene therapy Methods 0.000 description 16
- 208000028867 ischemia Diseases 0.000 description 16
- 230000001225 therapeutic effect Effects 0.000 description 16
- 238000004458 analytical method Methods 0.000 description 15
- 230000007423 decrease Effects 0.000 description 15
- 238000011161 development Methods 0.000 description 15
- 239000003550 marker Substances 0.000 description 15
- 238000004806 packaging method and process Methods 0.000 description 15
- 230000008859 change Effects 0.000 description 14
- 239000000835 fiber Substances 0.000 description 14
- 238000001476 gene delivery Methods 0.000 description 14
- 230000001976 improved effect Effects 0.000 description 14
- 230000006872 improvement Effects 0.000 description 14
- 230000001746 atrial effect Effects 0.000 description 13
- 230000004064 dysfunction Effects 0.000 description 13
- 102000005936 beta-Galactosidase Human genes 0.000 description 12
- 108010005774 beta-Galactosidase Proteins 0.000 description 12
- 238000002592 echocardiography Methods 0.000 description 12
- 210000005240 left ventricle Anatomy 0.000 description 12
- 230000004895 regional blood flow Effects 0.000 description 12
- 238000013518 transcription Methods 0.000 description 12
- 230000035897 transcription Effects 0.000 description 12
- 241001135569 Human adenovirus 5 Species 0.000 description 11
- 230000004217 heart function Effects 0.000 description 11
- 208000015181 infectious disease Diseases 0.000 description 11
- 210000004185 liver Anatomy 0.000 description 11
- 230000001588 bifunctional effect Effects 0.000 description 10
- 238000009434 installation Methods 0.000 description 10
- 230000001404 mediated effect Effects 0.000 description 10
- 102000004196 processed proteins & peptides Human genes 0.000 description 10
- 210000001147 pulmonary artery Anatomy 0.000 description 10
- 206010061218 Inflammation Diseases 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 230000027455 binding Effects 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- 239000003623 enhancer Substances 0.000 description 9
- 230000004054 inflammatory process Effects 0.000 description 9
- 210000002414 leg Anatomy 0.000 description 9
- 239000004005 microsphere Substances 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 108020005202 Viral DNA Proteins 0.000 description 8
- 150000001413 amino acids Chemical class 0.000 description 8
- AIYUHDOJVYHVIT-UHFFFAOYSA-M caesium chloride Chemical compound [Cl-].[Cs+] AIYUHDOJVYHVIT-UHFFFAOYSA-M 0.000 description 8
- 230000000004 hemodynamic effect Effects 0.000 description 8
- 238000007914 intraventricular administration Methods 0.000 description 8
- 108020004999 messenger RNA Proteins 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 230000009467 reduction Effects 0.000 description 8
- 230000002829 reductive effect Effects 0.000 description 8
- 210000002027 skeletal muscle Anatomy 0.000 description 8
- 238000007492 two-way ANOVA Methods 0.000 description 8
- 230000003313 weakening effect Effects 0.000 description 8
- 206010002383 Angina Pectoris Diseases 0.000 description 7
- 206010013975 Dyspnoeas Diseases 0.000 description 7
- 241000282887 Suidae Species 0.000 description 7
- 238000000540 analysis of variance Methods 0.000 description 7
- 238000010171 animal model Methods 0.000 description 7
- 210000000709 aorta Anatomy 0.000 description 7
- 230000008901 benefit Effects 0.000 description 7
- 230000037396 body weight Effects 0.000 description 7
- 238000009395 breeding Methods 0.000 description 7
- 230000001488 breeding effect Effects 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000002299 complementary DNA Substances 0.000 description 7
- 230000008828 contractile function Effects 0.000 description 7
- 239000012530 fluid Substances 0.000 description 7
- 208000019622 heart disease Diseases 0.000 description 7
- 230000000670 limiting effect Effects 0.000 description 7
- 210000004072 lung Anatomy 0.000 description 7
- 210000000107 myocyte Anatomy 0.000 description 7
- 238000000746 purification Methods 0.000 description 7
- 210000002966 serum Anatomy 0.000 description 7
- 230000008685 targeting Effects 0.000 description 7
- 238000001890 transfection Methods 0.000 description 7
- 208000000059 Dyspnea Diseases 0.000 description 6
- 241000282412 Homo Species 0.000 description 6
- 241000124008 Mammalia Species 0.000 description 6
- 208000009525 Myocarditis Diseases 0.000 description 6
- 206010028851 Necrosis Diseases 0.000 description 6
- 125000003275 alpha amino acid group Chemical group 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 6
- 238000012217 deletion Methods 0.000 description 6
- 230000037430 deletion Effects 0.000 description 6
- 238000002716 delivery method Methods 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 238000001802 infusion Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 230000010016 myocardial function Effects 0.000 description 6
- 230000017074 necrotic cell death Effects 0.000 description 6
- 102000039446 nucleic acids Human genes 0.000 description 6
- 108020004707 nucleic acids Proteins 0.000 description 6
- 150000007523 nucleic acids Chemical class 0.000 description 6
- 230000008488 polyadenylation Effects 0.000 description 6
- 238000003752 polymerase chain reaction Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 230000002685 pulmonary effect Effects 0.000 description 6
- 230000003362 replicative effect Effects 0.000 description 6
- 208000013220 shortness of breath Diseases 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000010186 staining Methods 0.000 description 6
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 6
- 229910052716 thallium Inorganic materials 0.000 description 6
- 108010084498 Myosin Heavy Chains Proteins 0.000 description 5
- 206010030113 Oedema Diseases 0.000 description 5
- 241000700159 Rattus Species 0.000 description 5
- 238000010162 Tukey test Methods 0.000 description 5
- 108010067390 Viral Proteins Proteins 0.000 description 5
- 230000001154 acute effect Effects 0.000 description 5
- 239000002870 angiogenesis inducing agent Substances 0.000 description 5
- 230000000692 anti-sense effect Effects 0.000 description 5
- 238000013459 approach Methods 0.000 description 5
- 230000009286 beneficial effect Effects 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000005538 encapsulation Methods 0.000 description 5
- 210000005003 heart tissue Anatomy 0.000 description 5
- 238000010348 incorporation Methods 0.000 description 5
- 210000005246 left atrium Anatomy 0.000 description 5
- 238000000386 microscopy Methods 0.000 description 5
- 229920001184 polypeptide Polymers 0.000 description 5
- 230000000750 progressive effect Effects 0.000 description 5
- 230000002035 prolonged effect Effects 0.000 description 5
- 210000005241 right ventricle Anatomy 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000012250 transgenic expression Methods 0.000 description 5
- 206010003445 Ascites Diseases 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 241000282472 Canis lupus familiaris Species 0.000 description 4
- 208000006029 Cardiomegaly Diseases 0.000 description 4
- 208000031229 Cardiomyopathies Diseases 0.000 description 4
- 206010016654 Fibrosis Diseases 0.000 description 4
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 4
- 208000037656 Respiratory Sounds Diseases 0.000 description 4
- 206010047924 Wheezing Diseases 0.000 description 4
- 238000010367 cloning Methods 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 239000002872 contrast media Substances 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 239000002552 dosage form Substances 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 230000002526 effect on cardiovascular system Effects 0.000 description 4
- 230000002169 extracardiac Effects 0.000 description 4
- 230000004761 fibrosis Effects 0.000 description 4
- 230000010354 integration Effects 0.000 description 4
- 210000004731 jugular vein Anatomy 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000004807 localization Effects 0.000 description 4
- 238000013507 mapping Methods 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 238000000424 optical density measurement Methods 0.000 description 4
- 235000015277 pork Nutrition 0.000 description 4
- 230000001737 promoting effect Effects 0.000 description 4
- 230000000644 propagated effect Effects 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- 230000000250 revascularization Effects 0.000 description 4
- 239000011435 rock Substances 0.000 description 4
- 238000001356 surgical procedure Methods 0.000 description 4
- 238000010361 transduction Methods 0.000 description 4
- 230000026683 transduction Effects 0.000 description 4
- 230000009261 transgenic effect Effects 0.000 description 4
- 238000005199 ultracentrifugation Methods 0.000 description 4
- YQNRVGJCPCNMKT-LFVJCYFKSA-N 2-[(e)-[[2-(4-benzylpiperazin-1-ium-1-yl)acetyl]hydrazinylidene]methyl]-6-prop-2-enylphenolate Chemical compound [O-]C1=C(CC=C)C=CC=C1\C=N\NC(=O)C[NH+]1CCN(CC=2C=CC=CC=2)CC1 YQNRVGJCPCNMKT-LFVJCYFKSA-N 0.000 description 3
- 101100462537 Caenorhabditis elegans pac-1 gene Proteins 0.000 description 3
- 208000001778 Coronary Occlusion Diseases 0.000 description 3
- 206010011086 Coronary artery occlusion Diseases 0.000 description 3
- 102000053602 DNA Human genes 0.000 description 3
- 108030001679 Endothelin-converting enzyme 1 Proteins 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 101100117764 Mus musculus Dusp2 gene Proteins 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229920005654 Sephadex Polymers 0.000 description 3
- 239000012507 Sephadex™ Substances 0.000 description 3
- 210000000683 abdominal cavity Anatomy 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 210000001054 cardiac fibroblast Anatomy 0.000 description 3
- 210000001715 carotid artery Anatomy 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 230000004087 circulation Effects 0.000 description 3
- 230000000120 cytopathologic effect Effects 0.000 description 3
- 230000034994 death Effects 0.000 description 3
- 230000007812 deficiency Effects 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 238000003745 diagnosis Methods 0.000 description 3
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003937 drug carrier Substances 0.000 description 3
- 210000001174 endocardium Anatomy 0.000 description 3
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 description 3
- 210000001508 eye Anatomy 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 229930182830 galactose Natural products 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 210000005260 human cell Anatomy 0.000 description 3
- 238000003384 imaging method Methods 0.000 description 3
- 230000028993 immune response Effects 0.000 description 3
- 238000003119 immunoblot Methods 0.000 description 3
- 230000002458 infectious effect Effects 0.000 description 3
- 210000004969 inflammatory cell Anatomy 0.000 description 3
- 239000002502 liposome Substances 0.000 description 3
- 210000004962 mammalian cell Anatomy 0.000 description 3
- 230000002503 metabolic effect Effects 0.000 description 3
- 239000002773 nucleotide Substances 0.000 description 3
- 125000003729 nucleotide group Chemical group 0.000 description 3
- 239000002953 phosphate buffered saline Substances 0.000 description 3
- 239000013641 positive control Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000004393 prognosis Methods 0.000 description 3
- 230000007425 progressive decline Effects 0.000 description 3
- 230000000069 prophylactic effect Effects 0.000 description 3
- 230000006798 recombination Effects 0.000 description 3
- 238000005215 recombination Methods 0.000 description 3
- 210000002345 respiratory system Anatomy 0.000 description 3
- 108091008146 restriction endonucleases Proteins 0.000 description 3
- 210000001525 retina Anatomy 0.000 description 3
- 230000001177 retroviral effect Effects 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 238000010561 standard procedure Methods 0.000 description 3
- 230000004936 stimulating effect Effects 0.000 description 3
- 230000009885 systemic effect Effects 0.000 description 3
- 238000002604 ultrasonography Methods 0.000 description 3
- 241001430294 unidentified retrovirus Species 0.000 description 3
- 210000005166 vasculature Anatomy 0.000 description 3
- 230000029812 viral genome replication Effects 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 2
- WOVKYSAHUYNSMH-RRKCRQDMSA-N 5-bromodeoxyuridine Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(Br)=C1 WOVKYSAHUYNSMH-RRKCRQDMSA-N 0.000 description 2
- 241000531891 Alburnus alburnus Species 0.000 description 2
- 208000023275 Autoimmune disease Diseases 0.000 description 2
- WOVKYSAHUYNSMH-UHFFFAOYSA-N BROMODEOXYURIDINE Natural products C1C(O)C(CO)OC1N1C(=O)NC(=O)C(Br)=C1 WOVKYSAHUYNSMH-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 description 2
- 206010014418 Electrolyte imbalance Diseases 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 208000024412 Friedreich ataxia Diseases 0.000 description 2
- 101710154606 Hemagglutinin Proteins 0.000 description 2
- 241000701024 Human betaherpesvirus 5 Species 0.000 description 2
- 206010020880 Hypertrophy Diseases 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 102100034343 Integrase Human genes 0.000 description 2
- 208000009378 Low Cardiac Output Diseases 0.000 description 2
- 229930195725 Mannitol Natural products 0.000 description 2
- 241001529936 Murinae Species 0.000 description 2
- 108091028043 Nucleic acid sequence Proteins 0.000 description 2
- 101710093908 Outer capsid protein VP4 Proteins 0.000 description 2
- 101710135467 Outer capsid protein sigma-1 Proteins 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 208000028872 Progressive muscular dystrophy Diseases 0.000 description 2
- 101710176177 Protein A56 Proteins 0.000 description 2
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 description 2
- 241000220317 Rosa Species 0.000 description 2
- 229920002684 Sepharose Polymers 0.000 description 2
- 208000009982 Ventricular Dysfunction Diseases 0.000 description 2
- 206010047281 Ventricular arrhythmia Diseases 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- GFFGJBXGBJISGV-UHFFFAOYSA-N adenyl group Chemical class N1=CN=C2N=CNC2=C1N GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 description 2
- 230000001800 adrenalinergic effect Effects 0.000 description 2
- 125000000539 amino acid group Chemical group 0.000 description 2
- 238000002399 angioplasty Methods 0.000 description 2
- 230000008321 arterial blood flow Effects 0.000 description 2
- 230000004872 arterial blood pressure Effects 0.000 description 2
- 230000002238 attenuated effect Effects 0.000 description 2
- 238000011888 autopsy Methods 0.000 description 2
- 102000012740 beta Adrenergic Receptors Human genes 0.000 description 2
- 108010079452 beta Adrenergic Receptors Proteins 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 238000001574 biopsy Methods 0.000 description 2
- 230000000157 blood function Effects 0.000 description 2
- 230000036772 blood pressure Effects 0.000 description 2
- 229950004398 broxuridine Drugs 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 150000003943 catecholamines Chemical class 0.000 description 2
- 238000004113 cell culture Methods 0.000 description 2
- 230000032823 cell division Effects 0.000 description 2
- 230000001413 cellular effect Effects 0.000 description 2
- 229940044683 chemotherapy drug Drugs 0.000 description 2
- 210000000349 chromosome Anatomy 0.000 description 2
- 230000001684 chronic effect Effects 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000006735 deficit Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 201000011304 dilated cardiomyopathy 1A Diseases 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000002934 diuretic Substances 0.000 description 2
- 229940030606 diuretics Drugs 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 210000002889 endothelial cell Anatomy 0.000 description 2
- 229940088598 enzyme Drugs 0.000 description 2
- 208000012955 familial cardiomyopathy Diseases 0.000 description 2
- 210000002950 fibroblast Anatomy 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000002523 gelfiltration Methods 0.000 description 2
- 239000000185 hemagglutinin Substances 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000001638 lipofection Methods 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- 239000000594 mannitol Substances 0.000 description 2
- 235000010355 mannitol Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 208000030159 metabolic disease Diseases 0.000 description 2
- 238000007431 microscopic evaluation Methods 0.000 description 2
- 230000002438 mitochondrial effect Effects 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 201000006938 muscular dystrophy Diseases 0.000 description 2
- 230000003274 myotonic effect Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229960002748 norepinephrine Drugs 0.000 description 2
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- XQYZDYMELSJDRZ-UHFFFAOYSA-N papaverine Chemical compound C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 XQYZDYMELSJDRZ-UHFFFAOYSA-N 0.000 description 2
- 230000037361 pathway Effects 0.000 description 2
- 101150063749 pcp-5 gene Proteins 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 238000011422 pharmacological therapy Methods 0.000 description 2
- 239000002504 physiological saline solution Substances 0.000 description 2
- 238000013310 pig model Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000004321 preservation Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000001566 pro-viral effect Effects 0.000 description 2
- 239000002331 radioactive microsphere Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 230000019491 signal transduction Effects 0.000 description 2
- 238000003307 slaughter Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 230000009870 specific binding Effects 0.000 description 2
- 238000007619 statistical method Methods 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 230000009897 systematic effect Effects 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000002103 transcriptional effect Effects 0.000 description 2
- 238000002054 transplantation Methods 0.000 description 2
- 238000010967 transthoracic echocardiography Methods 0.000 description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
- 210000002700 urine Anatomy 0.000 description 2
- 230000006815 ventricular dysfunction Effects 0.000 description 2
- 210000002845 virion Anatomy 0.000 description 2
- 238000001262 western blot Methods 0.000 description 2
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 1
- IQFYYKKMVGJFEH-OFKYTIFKSA-N 1-[(2r,4s,5r)-4-hydroxy-5-(tritiooxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione Chemical compound C1[C@H](O)[C@@H](CO[3H])O[C@H]1N1C(=O)NC(=O)C(C)=C1 IQFYYKKMVGJFEH-OFKYTIFKSA-N 0.000 description 1
- YSKMQAIZJHNDTP-UHFFFAOYSA-N 2-[4-[2-(3,5-dichloroanilino)-2-oxoethyl]phenoxy]-2-methylpropanoic acid Chemical compound C1=CC(OC(C)(C)C(O)=O)=CC=C1CC(=O)NC1=CC(Cl)=CC(Cl)=C1 YSKMQAIZJHNDTP-UHFFFAOYSA-N 0.000 description 1
- 101150096316 5 gene Proteins 0.000 description 1
- 229930008281 A03AD01 - Papaverine Natural products 0.000 description 1
- 208000010370 Adenoviridae Infections Diseases 0.000 description 1
- 206010060931 Adenovirus infection Diseases 0.000 description 1
- 229920000936 Agarose Polymers 0.000 description 1
- 241001182632 Akko Species 0.000 description 1
- 102000015427 Angiotensins Human genes 0.000 description 1
- 108010064733 Angiotensins Proteins 0.000 description 1
- 200000000007 Arterial disease Diseases 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 206010007558 Cardiac failure chronic Diseases 0.000 description 1
- 206010048610 Cardiotoxicity Diseases 0.000 description 1
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- 108020004705 Codon Proteins 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 102000029816 Collagenase Human genes 0.000 description 1
- 108060005980 Collagenase Proteins 0.000 description 1
- 206010069729 Collateral circulation Diseases 0.000 description 1
- 201000000057 Coronary Stenosis Diseases 0.000 description 1
- 206010011089 Coronary artery stenosis Diseases 0.000 description 1
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 description 1
- 241000701022 Cytomegalovirus Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 102000012410 DNA Ligases Human genes 0.000 description 1
- 108010061982 DNA Ligases Proteins 0.000 description 1
- 230000007023 DNA restriction-modification system Effects 0.000 description 1
- 241000208011 Digitalis Species 0.000 description 1
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 239000006145 Eagle's minimal essential medium Substances 0.000 description 1
- 102100036508 Elongin BC and Polycomb repressive complex 2-associated protein Human genes 0.000 description 1
- 208000005189 Embolism Diseases 0.000 description 1
- 101000896152 Escherichia phage Mu Baseplate protein gp47 Proteins 0.000 description 1
- 108700039887 Essential Genes Proteins 0.000 description 1
- 206010053487 Exposure to toxic agent Diseases 0.000 description 1
- 108700028146 Genetic Enhancer Elements Proteins 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 101800000194 Growth hormone-binding protein Proteins 0.000 description 1
- 102400001066 Growth hormone-binding protein Human genes 0.000 description 1
- 208000010496 Heart Arrest Diseases 0.000 description 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
- 101000852151 Homo sapiens Elongin BC and Polycomb repressive complex 2-associated protein Proteins 0.000 description 1
- 241000701131 Human adenovirus 14 Species 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 206010058558 Hypoperfusion Diseases 0.000 description 1
- YQEZLKZALYSWHR-UHFFFAOYSA-N Ketamine Chemical compound C=1C=CC=C(Cl)C=1C1(NC)CCCCC1=O YQEZLKZALYSWHR-UHFFFAOYSA-N 0.000 description 1
- 108090000362 Lymphotoxin-beta Proteins 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 108091034117 Oligonucleotide Proteins 0.000 description 1
- 108700026244 Open Reading Frames Proteins 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 208000018262 Peripheral vascular disease Diseases 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 108700008625 Reporter Genes Proteins 0.000 description 1
- 108091028664 Ribonucleotide Proteins 0.000 description 1
- 241000109329 Rosa xanthina Species 0.000 description 1
- 235000004789 Rosa xanthina Nutrition 0.000 description 1
- 101100220035 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CCZ1 gene Proteins 0.000 description 1
- 206010039491 Sarcoma Diseases 0.000 description 1
- 206010039897 Sedation Diseases 0.000 description 1
- 108020004682 Single-Stranded DNA Proteins 0.000 description 1
- 206010049418 Sudden Cardiac Death Diseases 0.000 description 1
- 210000001744 T-lymphocyte Anatomy 0.000 description 1
- 208000001871 Tachycardia Diseases 0.000 description 1
- 241001128391 Taia Species 0.000 description 1
- 206010052779 Transplant rejections Diseases 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 102000013534 Troponin C Human genes 0.000 description 1
- 108020000999 Viral RNA Proteins 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- HOBWAPHTEJGALG-JKCMADFCSA-N [(1r,5s)-8-methyl-8-azoniabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate;sulfate Chemical compound [O-]S([O-])(=O)=O.C([C@H]1CC[C@@H](C2)[NH+]1C)C2OC(=O)C(CO)C1=CC=CC=C1.C([C@H]1CC[C@@H](C2)[NH+]1C)C2OC(=O)C(CO)C1=CC=CC=C1 HOBWAPHTEJGALG-JKCMADFCSA-N 0.000 description 1
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000009102 absorption Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000021736 acetylation Effects 0.000 description 1
- 238000006640 acetylation reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000009692 acute damage Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000008649 adaptation response Effects 0.000 description 1
- 230000003044 adaptive effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 208000011589 adenoviridae infectious disease Diseases 0.000 description 1
- 239000000808 adrenergic beta-agonist Substances 0.000 description 1
- 229940009456 adriamycin Drugs 0.000 description 1
- 238000000246 agarose gel electrophoresis Methods 0.000 description 1
- VIROVYVQCGLCII-UHFFFAOYSA-N amobarbital Chemical compound CC(C)CCC1(CC)C(=O)NC(=O)NC1=O VIROVYVQCGLCII-UHFFFAOYSA-N 0.000 description 1
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 229960000723 ampicillin Drugs 0.000 description 1
- 230000003444 anaesthetic effect Effects 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 210000000702 aorta abdominal Anatomy 0.000 description 1
- 210000002565 arteriole Anatomy 0.000 description 1
- 208000028922 artery disease Diseases 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 229960002028 atropine sulfate Drugs 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000002146 bilateral effect Effects 0.000 description 1
- 102000023732 binding proteins Human genes 0.000 description 1
- 108091008324 binding proteins Proteins 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000036770 blood supply Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 210000002302 brachial artery Anatomy 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000007975 buffered saline Substances 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 239000007978 cacodylate buffer Substances 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 231100000259 cardiotoxicity Toxicity 0.000 description 1
- 210000000748 cardiovascular system Anatomy 0.000 description 1
- 230000022131 cell cycle Effects 0.000 description 1
- 230000003822 cell turnover Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 229960002424 collagenase Drugs 0.000 description 1
- 238000005094 computer simulation Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000003636 conditioned culture medium Substances 0.000 description 1
- 230000009091 contractile dysfunction Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 210000003748 coronary sinus Anatomy 0.000 description 1
- 239000012228 culture supernatant Substances 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 229960004397 cyclophosphamide Drugs 0.000 description 1
- 210000001151 cytotoxic T lymphocyte Anatomy 0.000 description 1
- 239000005547 deoxyribonucleotide Substances 0.000 description 1
- 125000002637 deoxyribonucleotide group Chemical group 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 108010060984 digitalis receptor Proteins 0.000 description 1
- 230000010339 dilation Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- 210000001198 duodenum Anatomy 0.000 description 1
- 238000004520 electroporation Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 230000003511 endothelial effect Effects 0.000 description 1
- 210000003038 endothelium Anatomy 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000002532 enzyme inhibitor Substances 0.000 description 1
- 230000001667 episodic effect Effects 0.000 description 1
- 239000013604 expression vector Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 208000004996 familial dilated cardiomyopathy Diseases 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 210000001105 femoral artery Anatomy 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- 230000013595 glycosylation Effects 0.000 description 1
- 238000006206 glycosylation reaction Methods 0.000 description 1
- 210000002288 golgi apparatus Anatomy 0.000 description 1
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 description 1
- 229960003132 halothane Drugs 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 210000002064 heart cell Anatomy 0.000 description 1
- 230000005986 heart dysfunction Effects 0.000 description 1
- 208000018578 heart valve disease Diseases 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 210000003494 hepatocyte Anatomy 0.000 description 1
- 238000010562 histological examination Methods 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- 210000003090 iliac artery Anatomy 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000028709 inflammatory response Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000004041 inotropic agent Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 229960003299 ketamine Drugs 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 210000003292 kidney cell Anatomy 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 208000010729 leg swelling Diseases 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000001926 lymphatic effect Effects 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 230000002297 mitogenic effect Effects 0.000 description 1
- 230000008747 mitogenic response Effects 0.000 description 1
- 230000000394 mitotic effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 230000003680 myocardial damage Effects 0.000 description 1
- 230000005914 myocardial expression Effects 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 210000001640 nerve ending Anatomy 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 231100001083 no cytotoxicity Toxicity 0.000 description 1
- 210000004940 nucleus Anatomy 0.000 description 1
- 230000030648 nucleus localization Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- SBUYBNIDQXQZSZ-UHFFFAOYSA-N p-aminophenylphosphocholine Chemical compound C[N+](C)(C)CCOP([O-])(=O)OC1=CC=C(N)C=C1 SBUYBNIDQXQZSZ-UHFFFAOYSA-N 0.000 description 1
- 229960001789 papaverine Drugs 0.000 description 1
- 210000003540 papillary muscle Anatomy 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 101150015232 pcp gene Proteins 0.000 description 1
- 210000003516 pericardium Anatomy 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000036581 peripheral resistance Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 239000002831 pharmacologic agent Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 230000007505 plaque formation Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000010837 poor prognosis Methods 0.000 description 1
- 230000004481 post-translational protein modification Effects 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000003334 potential effect Effects 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000001292 preischemic effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000009103 reabsorption Effects 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 230000022532 regulation of transcription, DNA-dependent Effects 0.000 description 1
- 230000001718 repressive effect Effects 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 230000036387 respiratory rate Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000002336 ribonucleotide Substances 0.000 description 1
- 125000002652 ribonucleotide group Chemical group 0.000 description 1
- 230000036280 sedation Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 230000037432 silent mutation Effects 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000001433 sodium tartrate Substances 0.000 description 1
- 229960002167 sodium tartrate Drugs 0.000 description 1
- 235000011004 sodium tartrates Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 208000014221 sudden cardiac arrest Diseases 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000006794 tachycardia Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 238000002627 tracheal intubation Methods 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000010474 transient expression Effects 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 241000712461 unidentified influenza virus Species 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 210000000264 venule Anatomy 0.000 description 1
- 108700026220 vif Genes Proteins 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1825—Fibroblast growth factor [FGF]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1858—Platelet-derived growth factor [PDGF]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1858—Platelet-derived growth factor [PDGF]
- A61K38/1866—Vascular endothelial growth factor [VEGF]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/30—Insulin-like growth factors, i.e. somatomedins, e.g. IGF-1, IGF-2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85277997A | 1997-05-06 | 1997-05-06 | |
PCT/US1998/008848 WO1998050079A2 (fr) | 1997-05-06 | 1998-04-30 | Techniques et compositions destinees au traitement d'une insuffisance cardiaque et du remodelage ventriculaire par apport in vivo de transgenes angiogeniques |
Publications (2)
Publication Number | Publication Date |
---|---|
EA199901002A1 EA199901002A1 (ru) | 2000-08-28 |
EA005157B1 true EA005157B1 (ru) | 2004-12-30 |
Family
ID=25314196
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA199901002A EA005157B1 (ru) | 1997-05-06 | 1998-04-30 | Методы и составы для лечения сердечной недостаточности и вентрикулярной коррекции путем доставки in vivo ангиогенных трансгенов |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP0980428A2 (fr) |
JP (1) | JP2002515065A (fr) |
KR (2) | KR20070005030A (fr) |
CN (1) | CN1267331A (fr) |
AU (1) | AU7173598A (fr) |
CA (1) | CA2289600C (fr) |
EA (1) | EA005157B1 (fr) |
WO (1) | WO1998050079A2 (fr) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2329934A1 (fr) * | 1998-05-30 | 1999-12-09 | Collateral Therapeutics, Inc. | Procedes de modification du phenotype de la cellule cardiaque |
DE19915485A1 (de) | 1999-04-07 | 2000-10-19 | Hugo A Katus | Therapie der Herzinsuffizienz |
NZ546670A (en) * | 1999-11-05 | 2009-02-28 | Univ California | Techniques and compositions for treating cardiovascular disease by in vivo gene delivery |
AU2002216751A1 (en) * | 2000-06-30 | 2002-01-14 | Collateral Therapeutics, Inc. | Dual recombinant gene therapy compositions and methods of use |
KR100562824B1 (ko) | 2002-03-20 | 2006-03-23 | 주식회사 바이로메드 | 유전자 발현효율이 높으며 간세포 성장인자의 두 가지이형체를 동시에 발현하는 하이브리드 간세포 성장인자유전자 |
US7875017B2 (en) | 2007-04-11 | 2011-01-25 | Henry Ford Health System | Cardiac repair, resizing and reshaping using the venous system of the heart |
EP2244740A1 (fr) | 2008-02-19 | 2010-11-03 | Celladon Corporation | Compositions pour un captage amélioré de vecteurs viraux dans le myocarde |
MX2010010993A (es) | 2008-04-09 | 2010-11-05 | Viromed Co Ltd | Formulaciones liofilizadas de adn para expresion mejorada de adn de plasmido. |
CN102076352B (zh) | 2008-05-02 | 2016-06-15 | 西安大略大学 | 与血管有关的fgf-9和它的用途 |
EP3311830A1 (fr) * | 2012-02-14 | 2018-04-25 | The Regents of The University of California | Administration systémique et expression régulée des gènes à action paracrine pour les maladies cardiovasculaires et autres états |
CN105682676B (zh) | 2013-10-22 | 2020-10-23 | 赫利世弥斯株式会社 | 利用肝细胞生长因子的两种以上的异构体的肌萎缩性侧索硬化症预防或治疗用组合物 |
AU2019305221A1 (en) | 2018-07-19 | 2021-02-18 | Helixmith Co., Ltd. | Lyophilized pharmaceutical compositions for naked DNA gene therapy |
CN109517807A (zh) * | 2018-11-20 | 2019-03-26 | 暨南大学 | 一种心脏血管靶向的噬菌体载体及其用途 |
EP3942018A4 (fr) * | 2019-03-17 | 2022-12-07 | Baylor College of Medicine | Reprogrammation directe de fibroblastes cardiaques en cardiomyocytes à l'aide d'une stratégie de transdifférenciation de cellules endothéliales |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0760682A4 (fr) * | 1995-02-28 | 1998-09-09 | Univ California | Therapie angiogenique par transfert de genes |
-
1998
- 1998-04-30 KR KR1020067026818A patent/KR20070005030A/ko not_active Application Discontinuation
- 1998-04-30 WO PCT/US1998/008848 patent/WO1998050079A2/fr active Application Filing
- 1998-04-30 JP JP54824398A patent/JP2002515065A/ja active Pending
- 1998-04-30 EA EA199901002A patent/EA005157B1/ru not_active IP Right Cessation
- 1998-04-30 EP EP98918904A patent/EP0980428A2/fr not_active Ceased
- 1998-04-30 CA CA2289600A patent/CA2289600C/fr not_active Expired - Fee Related
- 1998-04-30 CN CN98806526A patent/CN1267331A/zh active Pending
- 1998-04-30 AU AU71735/98A patent/AU7173598A/en not_active Abandoned
- 1998-04-30 KR KR1019997010265A patent/KR20010012313A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
KR20070005030A (ko) | 2007-01-09 |
KR20010012313A (ko) | 2001-02-15 |
CN1267331A (zh) | 2000-09-20 |
CA2289600A1 (fr) | 1998-11-12 |
JP2002515065A (ja) | 2002-05-21 |
AU7173598A (en) | 1998-11-27 |
EP0980428A2 (fr) | 2000-02-23 |
CA2289600C (fr) | 2010-06-29 |
EA199901002A1 (ru) | 2000-08-28 |
WO1998050079A3 (fr) | 1999-02-04 |
WO1998050079A2 (fr) | 1998-11-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6174871B1 (en) | Gene therapies for enhancing cardiac function | |
US5792453A (en) | Gene transfer-mediated angiogenesis therapy | |
US20090082293A1 (en) | Techniques and compositions for treating cardiovascular disease by in vivo gene delivery | |
EA005157B1 (ru) | Методы и составы для лечения сердечной недостаточности и вентрикулярной коррекции путем доставки in vivo ангиогенных трансгенов | |
AU784392B2 (en) | Techniques and compositions for treating cardiovascular disease by in vivo gene delivery | |
EP1695719A1 (fr) | Combinaision d'une acide nucléaire et d'un agent vasoactif pour l'amélioration de transfert de gènes | |
JP5623740B2 (ja) | 遺伝子治療用アデノ随伴ウイルスベクターの長期順行性の心外膜冠動脈注入 | |
AU706050C (en) | Gene transfer-mediated angiogenesis therapy | |
AU2006200170B2 (en) | Combination of a nucleic acid and a vasoactive agent for enhanced gene delivery | |
AU2006235836A1 (en) | Gene transfer-mediated angiogenesis therapy | |
AU4754199A (en) | Gene transfer-mediated angiogenesis therapy |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM RU |