| 摘要 |
Mixed chimerism induces donor-specific transplantation tolerance to organ allografts. Strategies to establish mixed chimerism using partial conditioning having significantly reduced the morbidity associated with conditioning. The donor hematopoietic cell lineage(s) responsible for the induction and subsequent maintenance of tolerance in partially conditioned recipients are not defined at present. As one approaches the threshold for nonmyeloablative conditioning, donor factors that influence the induction of tolerance have become apparent. In this invention, recipient B10 (H2<SUP>b</SUP>) mice were pretreated in vivo with anti-alphabeta-TCR and anti-CD8 mAbs 3 days before TBI (day 0) and transplanted with 15x10<SUP>6 </SUP>allogeneic (B10.BR;H2<SUP>k</SUP>) marrow cells. Engraftment occurred in 20%, 75% and 94% of animals conditioned with 100, 200 or 300 cGy TBI once month post BMT, respectively. In those animals that engrafted some exhibited multilineage production, including donor T cells, while others had only donor B cell, NK cell, macrophage, granulocyte and dendritic cell production. Animals without donor T cells lost their chimerism gradually within 6 months and rejected both donor and third-party skin grafts, even when they had significant (up to 70%) levels of donor chimerism. In animals with donor T cell production, chimerism remained stable for >_6 months and donor skin grafts were accepted. In the animals without donor T cell production, none of the expected stages of T cell development were present in the thymus, while in those with donor T cell production they were. Moreover, clonal deletion of Vbeta 5.1/2<SUP>+</SUP> and Vbeta 11<SUP>+</SUP> CD8 and CD4 T cells occurred only in chimeras with donor T cell production. These results show for the first time that donor T cell production plays a critical role in the maintenance of durable chimerism and induction of transplantation tolerance, and is directly correlated with deletion of potentially autoreactive cells.
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