Systemic delivery of human growth hormone or human factor IX in dogs by reintroduced genetically modified autologous bone marrow stromal cells

被引:88
作者
Hurwitz, DR
Kirchgesser, M
Merrill, W
Galanopoulos, T
McGrath, CA
Emami, S
Hansen, M
Cherington, V
Appel, JM
Bizinkauskas, CB
Brackmann, HH
Levine, PH
Greenberger, JS
机构
[1] MED CTR CENT MASSACHUSETTS, WORCESTER, MA 01605 USA
[2] UNIV BONN, INST EXPT HAMATOL & TRANSFUS MED, D-53105 BONN, GERMANY
关键词
D O I
10.1089/hum.1997.8.2-137
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Canine bone marrow stromal cells were expanded to numbers in excess of 10(9) cells from the initial 10-20 ml of marrow aspirates and transfected to express high levels of human growth hormone (hGH) in vitro. Ex vivo-modified marrow stromal cells were used in a gene therapy model system for the systemic delivery of transgene products in dogs. Adherent bone marrow stromal cell cultures, established and expanded from iliac crest marrow aspirates from each of 8 dogs, were transfected with a hGH gene plasmid expression vector and shown to express from 0.54-3.84 mu g/10(6) cells per 24 hr hGH in vitro. The transfected plasmid vector does not possess a eukaryotic origin of replication nor does it possess sequences required for efficient integration into the host cell genome. As such, expression was expected to be transient. Transfected cells were autologously reintroduced into each dog by either infusion into a foreleg vein or directly into iliac crest marrow. In two cases, the stromal cells were cryopreserved following transfection, and subsequently thawed and infused. In one case, the expanded stromal cells were first cryopreserved, and then thawed, recultured, transfected, and infused. Reintroduced cell numbers ranged from 2.2 x 10(7) to 2.6 x 10(9), with total hGH expression capacities ranging from 62 to 1,400 mu g/24 hr. Plasma of each of the dogs contained detectable hGH for a mean of 3.1 days (SD +/- 0.8 day) ranging from 2 to 5 days following reinfusion of cells. Peak plasma levels ranged from 0.10 to 1.76 ng/ml. Similar hGH expression values, based upon total expression capacity of the cells infused and dog body weight, were obtained for all dogs. Vector-modified stromal cells were detectable, by polymerase chain reaction (PCR) analysis, in the peripheral circulation following reinfusion in all 4 dogs analyzed. In 3 of the dogs, modified stromal cells were detected for 8.5-15 weeks. In addition, modified stromal cells were detected in iliac crest marrow of 2 dogs for 9 and 13 weeks, respectively, following reinfusion. Tn another experiment, cultured bone marrow stromal cells were transfected with a human factor IX (hFIX) plasmid vector. Modified cells (5.57 x 10(8)), with a total hFIX expression capacity of 281 mu g/24 hr, were reinfused, resulting in detectable hFIX in plasma continuously for 9 days with a peak level of 8 ng/ml on day 1. These results demonstrate that the ex vivo bone marrow stromal cell system is a potentially powerful method by which to deliver secreted transgene product to the systemic circulation of large animals.
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页码:137 / 156
页数:20
相关论文
共 67 条
[1]   SECRETION RATE OF HUMAN GROWTH-HORMONE .1. DAILY SECRETION RATES, EFFECT OF POSTURE AND SLEEP [J].
ALFORD, FP ;
BAKER, HWG ;
BURGER, HG .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1973, 37 (04) :515-520
[2]   CORRECTION OF THE GROWTH DEFECT IN DWARF MICE WITH NONAUTOLOGOUS MICROENCAPSULATED MYOBLASTS - AN ALTERNATE APPROACH TO SOMATIC GENE-THERAPY [J].
ALHENDY, A ;
HORTELANO, G ;
TANNENBAUM, GS ;
CHANG, PL .
HUMAN GENE THERAPY, 1995, 6 (02) :165-175
[3]  
Altman P.L., 1974, BIOL DATA BOOK
[4]  
ANKLESARIA P, 1989, BLOOD, V74, P1144
[5]   ENGRAFTMENT OF A CLONAL BONE-MARROW STROMAL CELL-LINE INVIVO STIMULATES HEMATOPOIETIC RECOVERY FROM TOTAL-BODY IRRADIATION [J].
ANKLESARIA, P ;
KASE, K ;
GLOWACKI, J ;
HOLLAND, CA ;
SAKAKEENY, MA ;
WRIGHT, JA ;
FITZGERALD, TJ ;
LEE, CY ;
GREENBERGER, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7681-7685
[6]   SYSTEMIC DELIVERY OF RECOMBINANT PROTEINS BY GENETICALLY MODIFIED MYOBLASTS [J].
BARR, E ;
LEIDEN, JM .
SCIENCE, 1991, 254 (5037) :1507-1509
[7]   A MAJORITY OF MICE SHOW LONG-TERM EXPRESSION OF A HUMAN BETA-GLOBIN GENE AFTER RETROVIRUS TRANSFER INTO HEMATOPOIETIC STEM-CELLS [J].
BENDER, MA ;
GELINAS, RE ;
MILLER, AD .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (04) :1426-1434
[8]  
BRETTLER DB, 1994, HEMOSTASIS THROMBOSI, P169
[9]  
CHANG PL, 1990, MOL BIOL MED, V7, P461
[10]  
CHERTKOV JL, 1985, EXP HEMATOL, V13, P1217