Antigen persistence and time of T-cell tolerization determine the efficacy of tolerization protocols for prevention of skin graft rejection

被引:51
作者
Ehl, S [1 ]
Aichele, P [1 ]
Ramseier, H [1 ]
Barchet, W [1 ]
Hombach, J [1 ]
Pircher, H [1 ]
Hengartner, H [1 ]
Zinkernagel, RM [1 ]
机构
[1] Univ Zurich, Dept Pathol, Inst Expt Immunol, CH-8091 Zurich, Switzerland
关键词
D O I
10.1038/2001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We studied antigen-specific T-cell tolerization therapy using skin transplantation across a defined minor histocompatibility antigen difference. Specific tolerization protocols using short-lived peptide or long-lived spleen cells presenting the peptide as antigen prevented graft rejection without immunosuppression when started before or as long as 10 days after transplantation. Peptide-induced T-cell tolerance was transient, and antigen presentation by the graft was not sufficient to maintain tolerance. In contrast, transfer of antigen-expressing lymphoid cells induced long-lasting tolerance correlating with donor cell chimerism. These findings show that antigen-specific tolerization can induce graft acceptance even when begun after transplantation and that long-term graft survival depends on persistence of the tolerizing antigen.
引用
收藏
页码:1015 / 1019
页数:5
相关论文
共 45 条
[1]   Peptide antigen treatment of naive and virus-immune mice: Antigen-specific tolerance versus immunopathology [J].
Aichele, P ;
BrduschaRiem, K ;
Oehen, S ;
Odermatt, B ;
Zinkernagel, RM ;
Hengartner, H ;
Pircher, H .
IMMUNITY, 1997, 6 (05) :519-529
[2]   T-CELL PRIMING VERSUS T-CELL TOLERANCE INDUCED BY SYNTHETIC PEPTIDES [J].
AICHELE, P ;
BRDUSCHARIEM, K ;
ZINKERNAGEL, RM ;
HENGARTNER, H ;
PIRCHER, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (01) :261-266
[3]   T cell tolerance and activation to a transgene-encoded tumor antigen [J].
Antoniou, A ;
McCormick, D ;
Scott, D ;
Yeoman, H ;
Chandler, P ;
Mellor, A ;
Dyson, J .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (05) :1094-1102
[4]   Protection against immunopathological consequences of a viral infection by activated but not resting cytotoxic T cells: T cell memory without ''memory T cells''? [J].
Bachmann, MF ;
Kundig, TM ;
Hengartner, H ;
Zinkernagel, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) :640-645
[5]   LONG-TERM RESULTS OF A CONTROLLED PROSPECTIVE-STUDY WITH TRANSFUSION OF DONOR-SPECIFIC BONE-MARROW IN 57 CADAVERIC RENAL-ALLOGRAFT RECIPIENTS [J].
BARBER, WH ;
MANKIN, JA ;
LASKOW, DA ;
DEIERHOI, MH ;
JULIAN, BA ;
CURTIS, JJ ;
DIETHELM, AG .
TRANSPLANTATION, 1991, 51 (01) :70-75
[6]   ACTIVELY ACQUIRED TOLERANCE OF FOREIGN CELLS [J].
BILLINGHAM, RE ;
BRENT, L ;
MEDAWAR, PB .
NATURE, 1953, 172 (4379) :603-606
[7]   MONOCLONAL-ANTIBODIES TO PROMOTE MARROW ENGRAFTMENT AND TISSUE GRAFT TOLERANCE [J].
COBBOLD, SP ;
MARTIN, G ;
QIN, S ;
WALDMANN, H .
NATURE, 1986, 323 (6084) :164-166
[8]  
DRESSER DW, 1962, IMMUNOLOGY, V5, P378
[9]   A functional and kinetic comparison of antiviral effector and memory cytotoxic T lymphocyte populations in vivo and in vitro [J].
Ehl, S ;
Klenerman, P ;
Aichele, P ;
Hengartner, H ;
Zinkernagel, RM .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (12) :3404-3413
[10]   Viral and bacterial infections interfere with peripheral tolerance induction and activate CD8+ T cells to cause immunopathology [J].
Ehl, S ;
Hombach, J ;
Aichele, P ;
Rülicke, T ;
Odermatt, B ;
Hengartner, H ;
Zinkernagel, R ;
Pircher, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (05) :763-774