Delivery of recombinant gene product to canine brain with the use of microencapsulation

被引:20
作者
Barsoum, SC
Milgram, W
Mackay, W
Coblentz, C
Delaney, KH
Kwiecien, JM
Kruth, SA
Chang, PL
机构
[1] McMaster Univ, Hlth Sci Ctr, Dept Pediat, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Hlth Sci Ctr, Dept Biol, Hamilton, ON L8N 3Z5, Canada
[3] McMaster Univ, Hlth Sci Ctr, Dept Radiol, Hamilton, ON L8N 3Z5, Canada
[4] McMaster Univ, Hlth Sci Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada
[5] Univ Toronto, Dept Psychol, Toronto, ON M5S 1A1, Canada
[6] Univ Toronto, Dept Physiol, Toronto, ON, Canada
[7] Univ Guelph, Dept Clin Studies, Guelph, ON N1G 2W1, Canada
来源
JOURNAL OF LABORATORY AND CLINICAL MEDICINE | 2003年 / 142卷 / 06期
关键词
D O I
10.1016/j.lab.2003.07.002
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
An alternative approach to somatic gene therapy is to deliver a therapeutic protein by implanting "universal" recombinant cells that are immunologically protected from graft rejection with alginate microcapsules. This strategy has proved successful in reversing pathologic conditions in several rodent models of human disease (dwarfism, lysosomal storage disease, hemophilia, cancer). In particular, neurologic disease and behavioral deficit in the mouse model of a neurodegenerative disease (mucopolysaccharidosis (MPS) VII) were significantly improved through the intraventricular implantation of the recombinant encapsulated cells. Here we report the feasibility of delivering recombinant gene products to the central nervous systems (CNSs) of dogs, first using human growth hormone as a marker for delivery in normal dogs and then using alpha-iduronidase as a therapeutic product for delivery in the MPS I dog that is genetically deficient in this lysosomal enzyme. Madin-Darby canine kidney cells were genetically modified to express either human growth hormone or canine a-iduronidase, then enclosed in alginate-poly-L-lysine-alginate microcapsules of about 500 mum in diameter. The encapsulated cells were implanted into the brain under steoreotaxic guidance. The brains were monitored with computed tomographic scans before and after surgery and examined biochemically and histologically. Delivery of gene products, as measured in the plasma and cerebrospinal fluid sampled periodically through 21 days or in various regions of the brain after death showed that the delivery of both gene products was extremely low but detectable. However, we noted extensive inflammatory reactions, both at the sites of implantation and in the immediate vicinity of the implanted microcapsules. Hence for this technology to be applicable to the CNSs of larger animals and human beings, a more accurate and less invasive neurosurgical procedure, more biocompatible microcapsule-recombinant cell combinations, and higher output of recombinant products must be developed.
引用
收藏
页码:399 / 413
页数:15
相关论文
共 42 条
[1]   TRANSPLANTATION OF NEURAL TISSUE IN POLYMER CAPSULES [J].
AEBISCHER, P ;
WINN, SR ;
GALLETTI, PM .
BRAIN RESEARCH, 1988, 448 (02) :364-368
[2]   Intrathecal delivery of CNTF using encapsulated genetically modified xenogeneic cells in amyotrophic lateral sclerosis patients [J].
Aebischer, P ;
Schluep, M ;
Deglon, N ;
Joseph, JM ;
Hirt, L ;
Heyd, B ;
Goddard, M ;
Hammang, JP ;
Zurn, AD ;
Kato, AC ;
Regli, F ;
Baetge, EE .
NATURE MEDICINE, 1996, 2 (06) :696-699
[3]   TRANSPLANTATION OF MICROENCAPSULATED BOVINE CHROMAFFIN CELLS REDUCES LESION-INDUCED ROTATIONAL ASYMMETRY IN RATS [J].
AEBISCHER, P ;
TRESCO, PA ;
SAGEN, J ;
WINN, SR .
BRAIN RESEARCH, 1991, 560 (1-2) :43-49
[4]   FUNCTIONAL RECOVERY IN HEMIPARKINSONIAN PRIMATES TRANSPLANTED WITH POLYMER-ENCAPSULATED PC12 CELLS [J].
AEBISCHER, P ;
GODDARD, M ;
SIGNORE, AP ;
TIMPSON, RL .
EXPERIMENTAL NEUROLOGY, 1994, 126 (02) :151-158
[5]   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
[6]  
ALLEN D, 1991, SMALL ANIMAL MED, P1076
[7]  
BARSOUM SC, 1999, THESIS MCMASTER U ON
[8]  
CHANG PL, 1990, MOL BIOL MED, V7, P461
[9]   The in vivo delivery of heterologous proteins by microencapsulated recombinant cells [J].
Chang, PL ;
Van Raamsdonk, JM ;
Hortelano, G ;
Barsoum, SC ;
MacDonald, NC ;
Stockley, TL .
TRENDS IN BIOTECHNOLOGY, 1999, 17 (02) :78-83
[10]  
Chang PL, 1995, SOMATIC GENE THERAPY, P203