Inducing tolerance to a soluble foreign antigen by encapsulated cell transplants

被引:7
作者
Blanco-Bose, WE [1 ]
Schneider, BL [1 ]
Aebischer, P [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Swiss Fed Inst Technol, Inst Neurosci, CH-1015 Lausanne, Switzerland
关键词
encapsulation; allogeneic transplantation; tolerance; immune response; soluble proteins;
D O I
10.1016/j.ymthe.2005.08.010
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
The immune response to soluble antigens constitutes a current clinical problem impeding the development of protein therapeutics. We have developed an encapsulated-cell delivery system, which, transiently combined with an anti-CD154 antibody treatment, allows for the suppression of this immune response and the establishment of long-term secretion of a foreign antigen, human erythropoietin (huEPO). The chronic presence of antigen appears to be required to maintain this tolerance, as a 21-day gap in the exposure to huEPO is sufficient to restore the ability of mice to mount an antibody response. In contrast, chronic huEPO expression maintains tolerance even in the absence of further anti-CD154 treatment. These results suggest that a soluble antigenic protein can be continuously released, without inducing an antibody response, using encapsulated allogeneic cells. The temporary anti-CD154 treatment induces immune unresponsiveness to the delivered antigen, while the immunoprotected cell implant allows for chronic antigen release, favoring the establishment of tolerance.
引用
收藏
页码:447 / 456
页数:10
相关论文
共 39 条
[31]   A self-immunomodulating myoblast cell line for erythropoietin delivery [J].
Schneider, BL ;
Peduto, G ;
Aebischer, P .
GENE THERAPY, 2001, 8 (01) :58-66
[32]   Long-term doxycycline-regulated secretion of erythropoietin by encapsulated myoblasts [J].
Sommer, B ;
Rinsch, C ;
Payen, E ;
Dalle, B ;
Schneider, B ;
Déglon, N ;
Henri, A ;
Beuzard, Y ;
Aebischer, P .
MOLECULAR THERAPY, 2002, 6 (02) :155-161
[33]  
Tibell A, 2001, CELL TRANSPLANT, V10, P591
[34]   Asialo GM1+ CD8+ T cells play a critical role in costimulation blockade-resistant allograft rejection [J].
Trambley, J ;
Bingaman, AW ;
Lin, A ;
Elwood, ET ;
Waitze, SY ;
Ha, JW ;
Durham, MM ;
Corbascio, M ;
Cowan, SR ;
Pearson, TC ;
Larsen, CP .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (12) :1715-1722
[35]   Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors [J].
Tripathy, SK ;
Black, HB ;
Goldwasser, E ;
Leiden, JM .
NATURE MEDICINE, 1996, 2 (05) :545-550
[36]   Mechanisms of transplant tolerance induction using costimulatory blockade [J].
Wekerle, T ;
Kurtz, J ;
Bigenzahn, S ;
Takeuchi, Y ;
Sykes, M .
CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (05) :592-600
[37]   Very high cost treatment for a single individual - a case report [J].
Wight, J ;
Richards, M .
JOURNAL OF PUBLIC HEALTH MEDICINE, 2003, 25 (01) :4-7
[38]   SERIAL PASSING AND DIFFERENTIATION OF MYOGENIC CELLS ISOLATED FROM DYSTROPHIC MOUSE MUSCLE [J].
YAFFE, D ;
SAXEL, O .
NATURE, 1977, 270 (5639) :725-727
[39]   Blockade of CD40L/CD40 costimulatory pathway in a DST presensitization model of islet allograft leads to a state of allo-Ag specific tolerance and permits subsequent engraftment of donor strain islet or heart allografts [J].
Zheng, XX ;
Li, Y ;
Li, XC ;
Roy-Chaudhury, P ;
Nickerson, P ;
Tian, Y ;
Sayegh, MH ;
Strom, TB .
TRANSPLANTATION PROCEEDINGS, 1999, 31 (1-2) :627-628