An essential role for Fas ligand in transplantation tolerance induced by donor bone marrow

被引:83
作者
George, JF
Sweeney, SD
Kirklin, JK
Simpson, EM
Goldstein, DR
Thomas, JM
机构
[1] Univ Alabama, Dept Surg, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Med, Birmingham, AL 35294 USA
[3] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
D O I
10.1038/nm0398-333
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
Medawar and co-workers originally demonstrated that injection of donor bone marrow (DBM) into immune-incompetent neonatal rodents could induce tolerance to grafts from animals of the same strain as the bone marrow donor(1). Induction of tolerance in this manner can also be accomplished in mature mice, dogs and monkeys if the resident T-cell populations in the recipient are depleted by a polyclonal antithymocyte globulin or an anti-T cell immunotoxin(2-4.) The molecular mechanisms by which bone marrow cells mediate the induction of tolerance remain uncertain. Here we examined a well-established adult mouse model of antithymocyte globulin and DBM treatment and show that expression of functional pas ligand (Fast, also CD95L) an the injected bone marrow cells is required for tolerance induction. The results indicate that a state of microchimerism per se is insufficient for the induction of tolerance in T cell-depleted transplant recipients. Moreover, the results are consistent with the hypothesis that tolerance induced by DBM involves an apoptotic process leading to deletion of graft-reactive cells.
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页码:333 / 335
页数:3
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