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1 xicity comparable to that of matched-sibling donor leukocyte infusion.
2  recipients treated with DNA vaccination and donor leukocyte infusion.
3 mmarizes recent data on the use of unrelated-donor leukocyte infusion.
4 cutaneous graft-versus-host disease, without donor leukocyte infusion.
5 lapse after allogeneic transplantation using donor leukocyte infusions.
6                                              Donor leukocyte infusions (1x10(7) /kg CD3+ T cells) wer
7   Extensive data are available on the use of donor leukocyte infusion after matched-sibling stem cell
8 but reports are remarkably few on the use of donor leukocyte infusion after unrelated-donor stem cell
9                                              Donor leukocyte infusions after allogeneic bone marrow t
10 eneic peripheral blood cell transplantation, donor leukocyte infusions, and unrelated bone marrow tra
11                                              Donor leukocyte infusion (DLI) can induce graft-versus-l
12                                     In mice, donor leukocyte infusion (DLI) given to established mixe
13 r role in another model involving delayed B6 donor leukocyte infusion (DLI) to established mixed allo
14                        A disease response to donor leukocyte infusion (DLI) was seen in 10 of 14 pati
15 ents achieved complete donor chimerism after donor leukocyte infusion (DLI).
16 l transplantation (alloHSCT) can be cured by donor leukocyte infusion (DLI); however, the cellular me
17                 The efficacy and toxicity of donor leukocyte infusions (DLI) after unrelated donor bo
18            Therapy of recurrent disease with donor leukocyte infusions (DLI) has been proven to be ef
19                                              Donor leukocyte infusions (DLI) in the allogeneic hemato
20                  Adoptive immunotherapy with donor leukocyte infusions (DLI) results in complete remi
21  effect has been provided by the efficacy of donor leukocyte infusions (DLI).
22 y alone, second myeloablative transplant, or donor leukocyte infusions (DLIs) alone is unusual.
23                  We evaluated HLA-compatible donor leukocyte infusions (DLIs) and HLA-compatible or H
24 llowing bone marrow transplantation, delayed donor leukocyte infusions (DLIs) can induce graft-versus
25                   Histocompatible allogeneic donor leukocyte infusions (DLIs) were administered as pr
26 together with the known antitumor effects of donor leukocyte infusions (DLIs), led to the design of t
27        In vitro analysis of splenocytes from donor leukocyte infusion donor mice demonstrated that im
28  Several case studies suggest that unrelated-donor leukocyte infusion effectively induces direct graf
29 ive allogeneic stem cell transplantation and donor leukocyte infusion for the induction of graft vers
30                       In this murine system, donor leukocyte infusion from a donor immunized with the
31                                              Donor leukocyte infusion further enhances tumor-free sur
32 nsplantation has led to the use of unrelated-donor leukocyte infusion in many patients.
33      There is a paucity of data on unrelated-donor leukocyte infusion in this setting.
34                   But the role for unrelated-donor leukocyte infusion is not well established.
35                 Expression of MHC class I on donor leukocyte infusions is important for overcoming re
36                                              Donor leukocyte infusions provide direct and potent graf
37 d transplant and three of three who received donor leukocyte infusions) remain alive.
38                      The dramatic success of donor leukocyte infusion to treat relapse after matched-
39                The effects of posttransplant donor leukocyte infusions to treat or prevent cytomegalo

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