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1 ans for augmenting the GVL effect of delayed donor lymphocyte infusion.
2 the graft-versus-leukemia effects of delayed donor lymphocyte infusion.
3 by day 200 after cyclosporine withdrawal and donor lymphocyte infusion.
4 rdizing the graft-versus-leukaemia effect of donor lymphocyte infusion.
5 sease occurred in 5 of 14 RIC patients after donor lymphocyte infusion.
6 5 days post-transplantation and responded to donor lymphocyte infusion.
7  resolved after treatment with rituximab and donor lymphocyte infusion.
8 nd one was reinduced into continuous CR with donor lymphocyte infusion.
9 omplete donor chimerism without the need for donor lymphocyte infusion.
10  of the anti-leukemia response in vivo after donor lymphocyte infusion.
11  a complete cytogenetic remission after CD4+ donor lymphocyte infusion.
12 se (GVHD), and the toxic effects of adjuvant donor-lymphocyte infusion.
13 GVHD and seven (14%) had chronic GVHD before donor-lymphocyte infusion.
14 unotherapy of hematologic malignancies using donor lymphocyte infusions.
15 found to inhibit the GVL response of delayed donor lymphocyte infusions.
16 l transplantation (alloTCD-HSCT) followed by donor lymphocyte infusions.
17 e response with reduced immunosuppression or donor lymphocyte infusions.
18 pse either prior to or during treatment with donor lymphocyte infusions.
19 ent was accomplished only following multiple donor lymphocyte infusions.
20 s a platform for adoptive immunotherapy with donor lymphocyte infusions.
21                    The sensitivity of CML to donor lymphocyte infusion after allogeneic stem cell tra
22        The majority of patients treated with donor lymphocyte infusions after relapse responded, demo
23 xperienced a complete remission after CD4(+) donor lymphocyte infusions also developed high-titer ant
24 e use of immune modulating therapies such as donor lymphocyte infusion and azacitidine.
25 ere isolated from peripheral blood after CD4 donor lymphocyte infusion and recognition of donor-deriv
26             Such treatment, as an adjunct to donor lymphocyte infusions and pharmacologic therapy, ma
27                                              Donor lymphocyte infusions are associated with a signifi
28                                              Donor lymphocyte infusions are extremely effective for c
29 phenotype, were administered as a preemptive donor lymphocyte infusion at day 14 post-HCT.
30               Ten patients received low-dose donor lymphocyte infusions beginning 5 months after tran
31                     Twelve patients received donor lymphocyte infusions +/- chemoimmunotherapy for re
32      Thirteen patients had undergone salvage donor lymphocyte infusion (DLI) (median time from DLI to
33 c cells, we assessed whether GVHD induced by donor lymphocyte infusion (DLI) affects the persistence,
34                   CD8+ T cell-depleted (TCD) donor lymphocyte infusion (DLI) after TCD allogeneic hem
35   Ten dogs also received escalating doses of donor lymphocyte infusion (DLI) alone or with pentostati
36  LVL (mean, 11 L) to collect lymphocytes for donor lymphocyte infusion (DLI) and other therapies was
37            In addition, 17 patients received donor lymphocyte infusion (DLI) as interventional therap
38 geneic stem cell graft followed by postponed donor lymphocyte infusion (DLI) can experience graft-ver
39                                              Donor lymphocyte infusion (DLI) can restore complete rem
40                                              Donor lymphocyte infusion (DLI) can restore durable mole
41    In the current study, we examined whether donor lymphocyte infusion (DLI) could be used as adoptiv
42 raft-versus-leukemia-based therapies such as donor lymphocyte infusion (DLI) for chronic myelogenous
43 te for patients who achieved remission after donor lymphocyte infusion (DLI) for progression, was 65%
44                                              Donor lymphocyte infusion (DLI) has been used in postnat
45                                              Donor lymphocyte infusion (DLI) has been used to enhance
46 atched, nonmyeloablative allogeneic SCT with donor lymphocyte infusion (DLI) in patients with lymphoi
47 (MMB3.19) were administered 7 days following donor lymphocyte infusion (DLI) or RLI on day 35.
48 geneic bone marrow transplantation (BMT) and donor lymphocyte infusion (DLI) provide valuable treatme
49                                              Donor lymphocyte infusion (DLI) re-establishes failing g
50                                              Donor lymphocyte infusion (DLI) reliably induces durable
51                                 Prophylactic donor lymphocyte infusion (DLI) strategies are recommend
52                    Delayed administration of donor lymphocyte infusion (DLI) to established mixed chi
53                                              Donor lymphocyte infusion (DLI) was administered in 26 e
54         Fifty-three of 446 patients received donor lymphocyte infusion (DLI) with a median CD3 dose o
55                                              Donor lymphocyte infusion (DLI), a standard relapse trea
56 ulations play a critical role in response to donor lymphocyte infusion (DLI), an established and pote
57 lant may achieve durable remission following donor lymphocyte infusion (DLI), showing the potency of
58                                              Donor lymphocyte infusion (DLI), whereby donor mononucle
59 their phenotype, and their role in governing donor lymphocyte infusion (DLI)-mediated alloresponses.
60 ion; 2 of these patients received concurrent donor lymphocyte infusion (DLI).
61 ute hepatitislike presentation of GVHD after donor lymphocyte infusion (DLI).
62 ow grafts, exceeding the survival benefit of donor lymphocyte infusion (DLI).
63 verted to full donor chimerism by the use of donor lymphocyte infusion (DLI; P = .03).
64  performed of the response to treatment with donor lymphocyte infusions (DLI) and the survival in 66
65                                              Donor lymphocyte infusions (DLI) can induce remissions i
66                     The clinical efficacy of donor lymphocyte infusions (DLI) in patients with relaps
67                                              Donor lymphocyte infusions (DLI) provide effective thera
68  disease (GVHD) by delayed administration of donor lymphocyte infusions (DLI) to established mixed ch
69                  We evaluated the ability of donor lymphocyte infusions (DLI) to mediate GVL effects
70 cal immunosuppression on the in vivo fate of donor lymphocyte infusions (DLI)-derived T cells, their
71                                   The use of donor lymphocytes infusion (DLI) continues to treat rela
72                         The effectiveness of donor-lymphocyte infusion (DLI) for treatment of relapse
73  lymphocytes from the original marrow donor (donor lymphocyte infusions [DLI]) is remarkably effectiv
74                                              Donor lymphocyte infusions (DLIs) 35 days after bone mar
75 tem cell transplantation (HSCT) and received donor lymphocyte infusions (DLIs) after transplantation.
76 after reduced-intensity allografts and while donor lymphocyte infusions (DLIs) can be effective salva
77 of this strategy remains of interest because donor lymphocyte infusions (DLIs) can induce a potent gr
78                                              Donor lymphocyte infusions (DLIs) can produce lasting re
79 nancies often are treated with unmanipulated donor lymphocyte infusions (DLIs) from the transplant do
80     We describe the toxicity and efficacy of donor lymphocyte infusions (DLIs) given to 81 patients (
81                                              Donor lymphocyte infusions (DLIs) induce effective graft
82                                              Donor lymphocyte infusions (DLIs) induce potent graft ve
83 y the mechanisms governing the activation of donor lymphocyte infusions (DLIs) manifesting as lymphoh
84             We aimed to assess the impact of donor lymphocyte infusions (DLIs) on relapse incidence w
85                               The ability of donor lymphocyte infusions (DLIs) to induce complete res
86                                              Donor lymphocyte infusions (DLIs) were given to 14 patie
87                  Dendritic cell vaccines and donor lymphocyte infusions (DLIs) were incorporated into
88 ent of animals with NST, posttransplantation donor lymphocyte infusions (DLIs), and a vaccine, compri
89 y that persisted after alloHSCT and standard donor lymphocyte infusions (DLIs).
90 ronic myeloid leukemia patients who received donor lymphocyte infusions following transplant relapse.
91 ntation is being explored through the use of donor lymphocyte infusions for patients who have relapse
92                                              Donor lymphocyte infusions for treatment of relapse afte
93                   16 (33%) patients received donor-lymphocyte infusion from 3 months after transplant
94                                        Since donor lymphocyte infusions have clinical activity in JMM
95 n proven by the demonstration of response to donor lymphocyte infusion in patients relapsing after al
96        The ability to induce remissions with donor lymphocyte infusion in patients with CLL, Richter'
97 evidence for its presence is the efficacy of donor lymphocyte infusions in generating anti-tumor resp
98                                              Donor lymphocyte infusion induced GVHD in nine of 23 pat
99                               Unfortunately, donor lymphocyte infusion induced severe cortisone-resis
100  hematopoietic stem cell transplantation and donor lymphocyte infusion is essential for acute graft v
101                   Prophylactic or preemptive donor lymphocyte infusion may be useful, but requires co
102                                              Donor lymphocyte infusions may also be used both prophyl
103 osuppression, antiviral therapy, unprocessed donor lymphocyte infusion, mobilized peripheral blood pr
104 meliorated the severity of GVHD in a delayed donor lymphocyte infusion model.
105 nt research is focusing on methods of making donor lymphocyte infusions more effective in the nonchro
106 ant cells or mixed chimerism could receive a donor lymphocyte infusion of 0.5 to 2 x 10(8) mononuclea
107 by cytoreductive therapy, followed either by donor lymphocyte infusion or second HSCT for consolidati
108 eduction of immune suppression plus or minus donor lymphocyte infusion or stem cell boost, which stab
109             Adjusting the timing and dose of donor lymphocyte infusion reduces the risk of graft-vers
110  patient peripheral blood at the time of the donor lymphocyte infusion response.
111                                   Subsequent donor lymphocyte infusion resulted in a significant chan
112 eated for relapsed MM after alloTCD-HSCT and donor lymphocyte infusions, supporting the development o
113      All types of cell-based therapies, from donor lymphocyte infusion to dendritic cell vaccines, an
114  chimerism in the presence of GVHD after CD4 donor lymphocyte infusion was observed in a patient, HLA
115                                              Donor lymphocyte infusions were given as part of the RIS
116                          Escalating doses of donor lymphocyte infusions were given from 6 months afte
117                                              Donor lymphocyte infusions were given to 18 patients eit
118 nd can preclude the administration of graded donor lymphocyte infusions, which may optimize the thera

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