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
[1]   INDUCTION OF TOLERANCE BY MONOCLONAL-ANTIBODY THERAPY [J].
BENJAMIN, RJ ;
WALDMANN, H .
NATURE, 1986, 320 (6061) :449-451
[2]   MECHANISMS OF MONOCLONAL ANTIBODY-FACILITATED TOLERANCE INDUCTION - A POSSIBLE ROLE FOR THE CD4 (L3T4) AND CD11A (LFA-1) MOLECULES IN SELF-NON-SELF DISCRIMINATION [J].
BENJAMIN, RJ ;
QIN, SX ;
WISE, MP ;
COBBOLD, SP ;
WALDMANN, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (07) :1079-1088
[3]   Pure red-cell aplasia and antierythropoietin antibodies in patients treated with recombinant erythropoietin. [J].
Casadevall, N ;
Nataf, J ;
Viron, B ;
Kolta, A ;
Kiladjian, J ;
Martin-Dupont, P ;
Michaud, P ;
Papo, T ;
Ugo, V ;
Teyssandier, I ;
Varet, B ;
Mayeux, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (07) :469-475
[4]   Antibodies against rHuEPO: native and recombinant [J].
Casadevall, N .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2002, 17 :42-47
[5]   ANALYTIC SOLUTIONS FOR THE FINITE-DIFFERENCE TIME-DOMAIN AND TRANSMISSION-LINE-MATRIX METHODS [J].
CHEN, ZZ ;
SILVESTER, PP .
MICROWAVE AND OPTICAL TECHNOLOGY LETTERS, 1994, 7 (01) :5-8
[6]  
DiMichele DM, 1998, HAEMOPHILIA, V4, P568
[7]  
DiMichele DM, 2002, THROMB HAEMOSTASIS, V87, P52
[8]   Cutting edge: Administration of anti-CD40 ligand and donor bone marrow leads to hemopoietic chimerism and donor-specific tolerance without cytoreductive conditioning [J].
Durham, MM ;
Bingaman, AW ;
Adams, AB ;
Ha, JW ;
Waitze, SY ;
Pearson, TC ;
Larsen, CP .
JOURNAL OF IMMUNOLOGY, 2000, 165 (01) :1-4
[9]   HUMAN T-CELL CLONAL ANERGY IS INDUCED BY ANTIGEN PRESENTATION IN THE ABSENCE OF B7 COSTIMULATION [J].
GIMMI, CD ;
FREEMAN, GJ ;
GRIBBEN, JG ;
GRAY, G ;
NADLER, LM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) :6586-6590
[10]   Dominant transplantation tolerance - Opinion [J].
Graca, L ;
Le Moine, A ;
Cobbold, SP ;
Waldmann, H .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (05) :499-506