Failure of donor lymphocyte infusion to prevent graft rejection in dogs given DLA-identical marrow after I Gy of total body irradiation

被引:7
作者
Baron, Fredric
Sandmaier, Brenda M.
Zellmer, Eustacia
Sorror, Mohamed
Storer, Bary
Storb, Rainer
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[2] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Dept Biostat, Seattle, WA USA
[4] Univ Liege, Dept Hematol, Liege, Belgium
关键词
hematopoietic cell transplantation; donor lymphocyte infusion; pentostatin; chimerism; nonmyeloablative; dog;
D O I
10.1016/j.bbmt.2006.05.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated in a preclinical canine model of hematopoietic cell transplantation (HCT) whether preemptive donor lymphocyte infusion (DLI) given 1 month after HCT could prevent late graft rejection that was the rule in historical dogs given suboptimal conditioning with 1 Gy of total body irradiation (TBI) before and immunosuppression with cyclosporine (CSP) and either mycophenolate mofetil (MMF; n = 6) or rapamycin (n = 5) after dog leukocyte antigen (DLA)-identical marrow transplantation. Nine dogs given DLA-identical marrow after I Gy of TBI followed by postgrafting MMF and CSP were studied. A single DLI was given 28-36 days after HCT, either with (n = 5) or without (n = 4) preceding treatment with the immunosuppressive drug pentostatin. Two of the 4 dogs given DLI only maintained stable mixed donor-host chimera beyond 30 weeks after HCT, whereas 2 rejected their grafts, on weeks 10 and 15 after HCT. One of the 5 dogs given pentostatin before DLI maintained a stable mixed donor-host chimera beyond 30 weeks, whereas 4 rejected their grafts, at weeks 8, 12, 12, and 16 after HCT. The 30-week probability of stable mixed chimerism, was 33% among dogs given DLI, versus 0% among 11 historical dogs (P = .003). In conclusion, DLI was only moderately effective in preventing graft rejection in this model. Additional immunosuppression with pentostatin did not improve that outcome. The model might be useful in developing potential strategies aimed at preventing graft rejection in patients with low donor chimerism, levels. (C) 2006 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:813 / 817
页数:5
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