Materials for immunoisolated cell transplantation

被引:91
作者
Li, RH [1 ]
机构
[1] CytoTherapeut Inc, Lincoln, RI 02865 USA
关键词
cell encapsulation; matrix; scaffold; membrane; gene therapy; microencapsulation; hollow fiber; polymer;
D O I
10.1016/S0169-409X(98)00022-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Encapsulated cell therapy provides site-specific continuous delivery of cell-synthesized molecules. Cell encapsulation therapy is based on the concept of immunoisolation. Foreign cells are surrounded with a semi-permeable membrane prior to transplantation to shield them from the host's natural defense system. This membrane is selectively permeable to transport of nutrients and therapeutic agents but relatively impermeable to larger molecules and cells of the hosts' immune system, Most encapsulation devices also utilize an internal matrix to keep cells suspended within the capsule. Proper choice of materials and materials processing techniques to formulate membrane and matrix components is essential to the success of these devices. A successful encapsulation device recreates the natural three-dimensional tissue environment that supports cell function and maintains cell viability. This review summarizes recent developments in materials development for cell encapsulation devices and highlights some ongoing challenges faced by those in the field. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:87 / 109
页数:23
相关论文
共 128 条
[1]   TRANSPLANTATION IN HUMANS OF ENCAPSULATED XENOGENEIC CELLS WITHOUT IMMUNOSUPPRESSION - A PRELIMINARY-REPORT [J].
AEBISCHER, P ;
BUCHSER, E ;
JOSEPH, JM ;
FAVRE, J ;
DETRIBOLET, N ;
LYSAGHT, M ;
RUDNICK, S ;
GODDARD, M .
TRANSPLANTATION, 1994, 58 (11) :1275-1277
[2]   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
[3]  
AEBISCHER P, 1991, BIOMATERIALS, P12
[4]  
AEBISCHER P, 1996, NAT MED, P2
[5]  
AEBISCHER P, 1993, FUNDAMENTALS ANIMAL, P7
[6]  
AEBISCHER P, 1986, T AM SOC ART INT ORG, V32, P134
[7]  
Alberts B., 1983, MOL BIOL CELL
[8]   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
[9]  
[Anonymous], [No title captured]
[10]  
Aung T, 1993, ASAIO J, V39, P93, DOI 10.1097/00002480-199304000-00004