Transplantation · 2000 · 26 citations · 6 references
Life SciencesImmunologyPharmacologyClinical ImmunologyKidney TransplantationTransplant ImmunologyAcute RejectionAllograft RejectionGraft RejectionGraft SurvivalImmunosuppression In Kidney TransplantationTransplant RejectionAcute Renal Allograft RejectionGraft Rejection ImmunobiologyImmunologic Response To AllograftMixed Lymphocyte ReactionRenal Transplant RejectionSkin GraftsT Cell - Mediated RejectionT-cell Mediated Rejection
BACKGROUND: In nonprimates, organ allografts are often not rejected after withdrawal of immunosuppression. In this study, we examined whether such a phenomenon also occurs in primates. METHODS: Vervet monkeys were transplanted with renal allografts and treated for 60 days with tacrolimus, or tacrolimus plus sirolimus. The drugs were totally withdrawn on day 61. The survival of the monkeys was monitored, and their response to donor- or third party-derived alloantigens was examined in vivo and in vitro. RESULTS: The majority (80-100%) of the grafts survived for at least additional 30 days with no signs of acute rejection. The compromised rejection is donor-specific, because recipient monkeys failed to reject a donor-derived skin graft, but a third-party skin graft was rejected. In vitro mixed lymphocyte reaction and interleukin-2 production in the mixed lymphocyte reaction between the recipients and their donors or between the recipients and a third party had no discernable patterns, and thus did not reflect the in vivo status of the immune system. Although the recipients could not reject the graft acutely after drug withdrawal, the kidney grafts and the donor-derived skin grafts had pathological findings of chronic rejection. CONCLUSIONS: The rejection response of the monkeys to an established graft after withdrawal of immunosuppression is compromised. The compromised rejection is specific and is not due to a permanent alteration of the immune system by the initial drug treatment. The allografts are not inert but have low levels of interaction with the recipient immune system.
6
SEQUENTIAL PROTOCOL BIOPSIES IN RENAL TRANSPLANT PATIENTS
David N. Rush, John Jeffery, James Gough · Transplantation · 1995 · 170 citations
Medicine, Nephrology, Pathology +17
INHIBITION OF IN VITRO IMMUNOGLOBULIN PRODUCTION BY RAPAMYCIN1
Hongyu Luo, Huifang Chen, Pierre Daloze et al. · Transplantation · 1992 · 70 citations
Rapamycin-induced long-term allograft survival depends on persistence of alloantigen.
H Chen, Hui Luo, Pierre Daloze et al. · The Journal of Immunology · 1994 · 27 citations · Full text