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1 emonstrate which NK cell subsets mediate the graft versus leukemia effect.
2 ural killer (NK) cells, key effectors of the Graft versus Leukemia effect.
3 , while maintaining immunocompetence and the graft versus leukemia effect.
4 n clinical trials while maintaining a robust graft-versus-leukemia effect.
5 ct of CMV infection has been reported on the graft-versus-leukemia effect.
6 hematologic diseases, with an often critical graft-versus-leukemia effect.
7 a means of decreasing GVHD while retaining a graft-versus-leukemia effect.
8 egies to predict a dominant unit and enhance graft-versus-leukemia effect.
9 cell dose on relapse may represent a delayed graft-versus-leukemia effect.
10  due to allogeneic disparities enhancing the graft-versus-leukemia effect.
11 tion and expansion in vivo, while preserving graft-versus-leukemia effects.
12 of human GVHD while ensuring conservation of graft-versus-leukemia effects.
13 f NK-cell-dependent in vivo cytotoxicity and graft-versus-leukemia effects.
14 e, which may have important implications for graft-versus-leukemia effects.
15 ls is crucial for promoting NK cell-mediated graft-versus-leukemia effects.
16 r adult recipients or an effective level of "graft-versus-leukemia" effect.
17 vaccines represent a strategy to enhance the graft-versus-leukemia effect after allogeneic blood and
18                             Despite observed graft-versus-leukemia effects after stem cell transplant
19                   Through an immune-mediated graft-versus-leukemia effect, allogeneic hematopoietic s
20 g the late establishment of a posttransplant graft-versus-leukemia effect and an overrepresentation o
21 ice with the advantages of possible stronger graft-versus-leukemia effect and expanding transplantati
22  outcomes, results of nonmyeloablative UCBT, graft-versus-leukemia effect and graft-versus-host disea
23  CML in chronic phase, its responsiveness to graft-versus-leukemia effect and the ability to monitor
24 nistered after BMT might induce or amplify a graft-versus-leukemia effect and thereby reduce the rela
25 e development of new strategies to enhance a graft-versus-leukemia effect and to decrease the inciden
26     Whether such differences will compromise graft-versus-leukemia effects and disease-free survival
27 as GVHD prophylaxis, Tregs potently suppress graft-versus-leukemia effects and so may be most appropr
28 nefit, the value of purging, the presence of graft-versus-leukemia effect, and the timing of transpla
29                        CLL is susceptible to graft-versus-leukemia effects, and allogeneic HCT after
30                                          The graft-versus-leukemia effect appeared effective, even in
31 elapse due to the lack of an immune-mediated graft-versus-leukemia effect, as occurs in the allogenei
32 al killer lymphocytes may play a role in the graft-versus-leukemia effect, attention is focusing incr
33 risk of early relapse/progression before the graft-versus-leukemia effect being disproportionally lar
34 or lymphocyte transfusions indicate that the graft-versus-leukemia effect can be very powerful and to
35 d fludarabine, relying almost exclusively on graft-versus-leukemia effects, can result in long-term r
36                   In addition to providing a graft-versus-leukemia effect, donor T cells are critical
37 at mediate graft-versus-host disease and the graft-versus-leukemia effect following stem cell transpl
38 ractions between HLA-C and KIR might promote Graft-versus-Leukemia effects following transplantation.
39 g the beneficial graft-versus-tumor (GVT) or graft-versus-leukemia effects from graft-versus-host dis
40 new immunotherapeutic approach to separating graft-versus-leukemia effects from GvHD.
41                                            A graft-versus-leukemia effect has been well documented to
42 e immune system will allow us to improve the graft-versus-leukemia effect, improve engraftment, and d
43 apse risk, this analysis reveals an enhanced graft-versus-leukemia effect in acute leukemia patients
44 lapse responded, demonstrating a significant graft-versus-leukemia effect in CLL.
45 DR15 on graft-versus-host disease (GVHD) and graft-versus-leukemia effects in HLA-matched allogeneic
46 ells was associated with decreased cGVHD and graft-versus-leukemia effects in recipients of allogenei
47                                          The graft-versus-leukemia effect is critical to the maintena
48                          The immune-mediated graft-versus-leukemia effect is important to prevent rel
49 ion for HLA-matched HCT may achieve superior graft versus leukemia effects, lower risk for relapse, a
50 tation can eradicate the leukemia and that a graft-versus-leukemia effect makes a major contribution
51                                          The graft-versus-leukemia effect of allogeneic stem-cell tra
52                MDSC-IL-13 did not reduce the graft-versus-leukemia effect of donor T cells.
53 ecipients was strikingly advantageous in the graft-versus-leukemia effects of delayed donor lymphocyt
54 monstration that an immunologically mediated graft-versus-leukemia effect plays a central role in del
55 of allogeneic cells and they rely largely on graft-versus-leukemia effects rather than high-dose cyto
56                 The regimens rely largely on graft-versus-leukemia effects rather than high-dose ther
57 e after allografting; the mechanism for this graft-versus-leukemia effect remains speculative.
58 re has been a corresponding reduction in the graft-versus-leukemia effect so that any decrease in GVH
59 al in a mouse model of aGVHD while retaining graft-versus-leukemia effects, unveiling a novel therape
60                                          The graft-versus-leukemia effect was initially considered to
61                                 Although the graft-versus-leukemia effect was predicted from animal e
62 cross the placenta and might confer a potent graft-versus-leukemia effect when cord blood (CB) is use
63 inally, T-bet(-/-) T cells had a compromised graft-versus-leukemia effect, which could be essentially
64 r immune reconstitution and a quite powerful graft-versus-leukemia effect with a low incidence of gra
65 ne response to these antigens may potentiate graft-versus-leukemia effect without accompanying graft-
66      This approach permits us to explore the graft-versus-leukemia effect without the toxicity of mye

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