Gene therapy for ischemic heart disease

被引:6
作者
Malosky, S
Kolansky, DM
机构
[1] Cardiovascular Division, 9 Founders Pavilion, Hosp. of the Univ. of Pennsylvania, Philadelphia, PA 19104
基金
美国国家卫生研究院;
关键词
D O I
10.1097/00001573-199607000-00004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gene therapy techniques are being developed as potential treatments for dyslipidemias, coronary restenosis, and vein graft disease. Retroviral and now adenoviral gene delivery techniques are being studied. A human protocol for the treatment of familial hypercholesterolemia has recently been completed using ex vivo hepatic low-density lipoprotein receptor gene transfer via a retroviral vector. Work in most other areas is currently in the animal model stage. Significant progress has been made in the area of coronary restenosis, particularly in identifying target genes to reduce neointima formation, such as herpesvirus thymidine kinase and the retinoblastoma gene, Work also continues in developing strategies to decrease neointima formation in vein grafts used in coronary bypass surgery and in improving methods of myocardial protection during surgery.
引用
收藏
页码:361 / 368
页数:8
相关论文
共 62 条
[31]   ADENOVIRUS-MEDIATED TRANSFER OF A RECOMBINANT HUMAN ALPHA-1-ANTITRYPSIN CDNA TO HUMAN ENDOTHELIAL-CELLS [J].
LEMARCHAND, P ;
JAFFE, HA ;
DANEL, C ;
CID, MC ;
KLEINMAN, HK ;
STRATFORDPERRICAUDET, LD ;
PERRICAUDET, M ;
PAVIRANI, A ;
LECOCQ, JP ;
CRYSTAL, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6482-6486
[32]   RETROVIRAL-MEDIATED GENE-TRANSFER AND EXPRESSION OF HUMAN LIPOPROTEIN-LIPASE IN SOMATIC-CELLS [J].
LEWIS, MES ;
FORSYTHE, IJ ;
MARTH, JD ;
BRUNZELL, JD ;
HAYDEN, MR ;
HUMPHRIES, RK .
HUMAN GENE THERAPY, 1995, 6 (07) :853-863
[33]   IN-VIVO GENE-THERAPY FOR HYPERLIPIDEMIA - PHENOTYPIC CORRECTION IN WATANABE RABBITS BY HEPATIC DELIVERY OF THE RABBIT LDL RECEPTOR GENE [J].
LI, J ;
FANG, BL ;
EISENSMITH, RC ;
LI, XHC ;
NASONKIN, I ;
LINLEE, YC ;
MIMS, MP ;
HUGHES, A ;
MONTGOMERY, CD ;
ROBERTS, JD ;
PARKER, TS ;
LEVINE, DM ;
WOO, SLC .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (02) :768-773
[34]   APOLIPOPROTEIN-E - CHOLESTEROL TRANSPORT PROTEIN WITH EXPANDING ROLE IN CELL BIOLOGY [J].
MAHLEY, RW .
SCIENCE, 1988, 240 (4852) :622-630
[35]   GENETIC-ENGINEERING OF VEIN GRAFTS RESISTANT TO ATHEROSCLEROSIS [J].
MANN, MJ ;
GIBBONS, GH ;
KERNOFF, RS ;
DIET, FP ;
TSAO, PS ;
COOKE, JP ;
KANEDA, Y ;
DZAU, VJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4502-4506
[36]   OVEREXPRESSION OF THE RAT INDUCIBLE 70-KD HEAT-STRESS PROTEIN IN A TRANSGENIC MOUSE INCREASES THE RESISTANCE OF THE HEART TO ISCHEMIC-INJURY [J].
MARBER, MS ;
MESTRIL, R ;
CHI, SH ;
SAYEN, MR ;
YELLON, DM ;
DILLMANN, WH .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1446-1456
[37]   CARDIAC STRESS PROTEIN ELEVATION 24 HOURS AFTER BRIEF ISCHEMIA OR HEAT-STRESS IS ASSOCIATED WITH RESISTANCE TO MYOCARDIAL-INFARCTION [J].
MARBER, MS ;
LATCHMAN, DS ;
WALKER, JM ;
YELLON, DM .
CIRCULATION, 1993, 88 (03) :1264-1272
[38]   PHARMACOKINETICS OF ADENOVIRAL VECTOR-MEDIATED GENE DELIVERY TO VASCULAR SMOOTH-MUSCLE CELLS - MODULATION BY POLOXAMER-407 AND IMPLICATIONS FOR CARDIOVASCULAR GENE-THERAPY [J].
MARCH, KL ;
MADISON, JE ;
TRAPNELL, BC .
HUMAN GENE THERAPY, 1995, 6 (01) :41-53
[39]  
MAZUR W, 1994, CORONARY ARTERY DIS, V5, P779
[40]   IMMEDIATE-EARLY GENE-EXPRESSION IN HUMAN SAPHENOUS VEINS HARVESTED DURING CORONARY-ARTERY BYPASS GRAFT OPERATIONS [J].
MOGGIO, RA ;
DING, JZ ;
SMITH, CJ ;
TOTA, RR ;
STEMERMAN, MB ;
REED, GE .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1995, 110 (01) :209-213