Spontaneous acceptance of liver transplants in rodents: Evidence that liver leucocytes induce recipient T-cell death by neglect

被引:42
作者
Bishop, GA
Wang, CM
Sharland, AF
McCaughan, GW
机构
[1] Centenary Inst Canc Med & Cell Biol, AW Morrow Gastroenterol & Liver Lab, Newtown, NSW 2042, Australia
[2] Royal Prince Alfred Hosp, Dept Transplant Surg, Sydney, NSW, Australia
关键词
graft rejection; graft survival; immunosuppressive agents; liver transplantation; transplantation tolerance;
D O I
10.1046/j.1440-1711.2002.01049.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In many animal models transplanted livers are not rejected, even when there is a complete MHC mismatch between the donor and recipient and the recipient is not immunosuppressed. This distinguishes liver transplants from other organs, such as kidneys and hearts, which are rapidly rejected in mismatched individuals. Acceptance of transplanted livers in a rat model is not due to the absence of an immune response to the liver and there is a rapid, abortive response that is ultimately exhausted. Donor leucocytes transferred with the liver appear to be responsible for both liver acceptance and the abortive activation of the recipient's T cells. The immune mechanism of liver transplant acceptance appears to be due to 'death by neglect' in which T cells are activated to express IL-2 and IFN-gamma mRNA in the recipient lymphoid tissues, but not at adequate levels within the graft. Subsequently the activated T cells die leading to specific clonal deletion of liver donor-reactive T cells. These findings have important implications for liver transplant patients as immunosuppressive drugs that are given to prevent rejection can also interfere with this form of tolerance. In addition, it might be possible to modify the immunosuppressive drug treatment of transplant patients to promote the process of death by neglect of recipient alloreactive T cells.
引用
收藏
页码:93 / 100
页数:8
相关论文
共 80 条
[51]   High-dose donor bone marrow infusions to enhance allograft survival - The effect of timing [J].
Ricordi, C ;
Karatzas, T ;
Nery, J ;
Webb, M ;
Selvaggi, G ;
Fernandez, L ;
Khan, FA ;
Ruiz, P ;
Schiff, E ;
Olson, L ;
Fernandez, H ;
Bean, J ;
Esquenazi, V ;
Miller, J ;
Tzakis, AG .
TRANSPLANTATION, 1997, 63 (01) :7-11
[52]  
Rokahr KL, 1998, IMMUNOLOGY, V95, P257
[53]   Kinetics of intragraft cytokine expression, cellular infiltration, and cell death in rejection of renal allografts compared with acceptance of liver allografts in a rat model - Early activation and apoptosis is associated with liver graft acceptance [J].
Sharland, A ;
Shastry, S ;
Wang, CM ;
Rokahr, K ;
Sun, JH ;
Sheil, AGR ;
McCaughan, GW ;
Bishop, GA .
TRANSPLANTATION, 1998, 65 (10) :1370-1377
[54]   Evidence that apoptosis of activated T cells occurs in spontaneous tolerance of liver allografts and is blocked by manipulations which break tolerance [J].
Sharland, A ;
Yan, YQ ;
Wang, CM ;
Bowen, DG ;
Sun, JH ;
Sheil, AGR ;
McCaughan, GW ;
Bishop, GA .
TRANSPLANTATION, 1999, 68 (11) :1736-1745
[55]  
Shimizu Y, 1996, TRANSPL INT, V9, P593
[56]   THE ESSENTIAL ROLES OF PARENCHYMAL TISSUES AND PASSENGER LEUKOCYTES IN THE TOLERANCE INDUCED BY LIVER GRAFTING IN RATS [J].
SRIWATANAWONGSA, V ;
DAVIES, HFS ;
CALNE, RY .
NATURE MEDICINE, 1995, 1 (05) :428-432
[57]   Liver transplants contribute to their own success [J].
Starzl, TE ;
Murase, N ;
Thomson, A ;
Demetris, AJ .
NATURE MEDICINE, 1996, 2 (02) :163-165
[58]   CELL-MIGRATION, CHIMERISM, AND GRAFT ACCEPTANCE [J].
STARZL, TE ;
DEMETRIS, AJ ;
MURASE, N ;
ILDSTAD, S ;
RICORDI, C ;
TRUCCO, M .
LANCET, 1992, 339 (8809) :1579-1582
[59]   SPECIFIC SUPPRESSION OF ALLOGRAFT-REJECTION BY SOLUBLE CLASS-I ANTIGEN AND COMPLEXES WITH MONOCLONAL-ANTIBODY [J].
SUMIMOTO, R ;
KAMADA, N .
TRANSPLANTATION, 1990, 50 (04) :678-682
[60]   TOLERANCE TO RAT-LIVER ALLOGRAFTS .1. DIFFERENCES BETWEEN TOLERANCE AND REJECTION ARE MORE MARKED IN THE B-CELL COMPARED WITH THE T-CELL OR CYTOKINE RESPONSE [J].
SUN, JH ;
MCCAUGHAN, GW ;
MATSUMOTO, Y ;
SHEIL, AGR ;
GALLAGHER, ND ;
BISHOP, GA .
TRANSPLANTATION, 1994, 57 (09) :1349-1357