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1 the presence of mature donor T cells in the marrow graft.
2 allogeneic, xenogeneic and missing self bone-marrow grafts.
3 y, on immune functions in six dogs not given marrow grafts.
4 1 Gy TBI and dog leukocyte antigen-identical marrow grafts.
5 so failed to inhibit rejection of TNFR1(-/-) marrow grafts.
6 DS/AML (RR = 1.8; P =.12) compared with bone marrow grafts.
7 ted mice receiving fully MHC-mismatched bone marrow grafts.
8 ntain about 10 times more T and B cells than marrow grafts.
9 T cells in unmanipulated PBSCs than in bone marrow grafts.
10 recipients transplanted with MHC-mismatched marrow grafts.
11 y irradiation and DLA-nonidentical unrelated marrow grafts.
12 major histocompatibility complex-mismatched marrow grafts.
13 eceiving blood transfusions or organ or bone marrow grafts.
14 reconstitution in recipients of MHC-matched marrow grafts.
15 osphamide, then were transplanted with CD34+ marrow grafts.
16 nd mismatched (B10.BR[H-2k] --> DBA/2[H-2d]) marrow grafts.
17 eparations disqualified the use of the CD34+ marrow grafts.
18 the specific antitumor effect of allogeneic marrow grafts.
19 n 72 patients surviving 20 to 30 years after marrow grafting.
22 In this model most animals rejected their marrow grafts after a preparative regimen of 9.2 Gy tota
24 e fail to reject fully mismatched allogeneic marrow grafts and show enhanced survival after such tran
26 100 cGy TBI, dog leukocyte antigen-identical marrow grafts, and mycophenolate mofetil/cyclosporine.
27 odel of hybrid resistance, in which parental marrow grafts are rejected solely by the NK cells of irr
28 randomized to receive an autologous CD34(+) marrow graft (Arm A) versus a standard buffy coat fracti
29 el, gzm B -/- hosts rejected haplo-identical marrow grafts as efficiently as did their wild-type litt
30 imary host barrier cells that recognize bone marrow grafts bearing hematopoietic histocompatibility a
32 tein-Barr virus (EBV) lymphomas complicating marrow grafts, but they contain alloreactive T cells cap
34 udies, we added mature donor T cells to bone marrow grafts combined with heart grafts, and compared m
36 facilitating engraftment, to T-cell depleted marrow grafts containing 160 x 10(6) activated gamma del
37 in allogeneic recipients of T-cell-depleted marrow grafts, exceeding the survival benefit of donor l
38 s of alpha beta T cells were required in the marrow graft for the eradication of residual host T cell
40 conditioning, simultaneous administration of marrow grafts from 2 DLA-identical littermates could res
42 35 days resulted in establishment of stable marrow grafts from DLA-identical canine littermates afte
43 ti-CD45 or anti-TCRalphabeta mAb followed by marrow grafts from DLA-identical littermates and postgra
44 Accordingly, 12 dogs were given 9.2 Gy TBI, marrow grafts from DLA-mismatched unrelated dogs, and a
45 total-body irradiation (TBI) and unmodified marrow grafts from dog leukocyte antigen (DLA)-identical
46 Previous studies have demonstrated that most marrow grafts from dog leukocyte antigen (DLA)-mismatche
47 s with hematologic malignancies who received marrow grafts from either phenotypically matched unrelat
48 and 58 mismatched) and 48 patients received marrow grafts from family donors that were mismatched at
49 essed in 17 patients who received allogeneic marrow grafts from HLA-matched siblings between 1971 and
52 se, 0.1-5.9 mCi/kg [3.7-218 MBq/kg]) without marrow grafts had no toxic effects other than a mild, re
54 e that recipients of both unmodified and TCD marrow grafts have profound deficiencies of EBV-specific
55 st-generation back-crossed mice rejected H2b marrow grafts (hybrid resistance), transgene-positive mi
56 R] = 1.4; P < .0001), blood cell versus bone marrow grafts in patients age 18 to 39 years (RR = 1.43;
57 Ralphabeta prevented rejection of allogeneic marrow grafts in the setting of conditioning with a rela
58 pregnancy and healthy childbirth after bone marrow grafting is relatively rare due to irradiation, b
61 eks after transplantation, and hCD34(+) bone marrow grafts of primary recipients could reconstitute h
62 CR T cells in arrbetagal mice by use of bone marrow grafts, or double-transgenic mice, also gave no r
63 ipient CD8 effectors responsible for causing marrow graft rejection are sensitive to cytotoxicity med
65 To evaluate whether the ability to prevent marrow graft rejection could be dissociated from the abi
71 We conclude that Tc2 cells potently inhibit marrow graft rejection without inducing an alloaggressiv
72 + T cells capable of host reactivity inhibit marrow graft rejection, but also generate graft-versus-h
73 LA-A or HLA-B antigens increases the risk of marrow graft rejection, but the relevance of HLA-C is un
74 se T cells and NK cells are critical in bone marrow graft rejection, our purpose was to examine wheth
75 play a pivotal role in preventing allogeneic marrow graft rejection, possibly by generating cytotoxic
81 der versus age 18 to 39 years receiving bone marrow grafts (RR = 1.44; P = .0005), CML versus AML/ALL
83 e (GVHD) was lower with T-cell-depleted bone marrow grafts; T-cell-depleted grafts were not associate
84 er, these data support the results from bone marrow grafts that circulating CD11b+ cells can enter th
85 naive gamma delta T cells to T-cell depleted marrow grafts was required to significantly increase all
86 n one log more T lymphocytes than unmodified marrow grafts, we evaluated the incidence of chronic GVH
89 he exception of recipients of haploidentical marrow grafts, who received antithymocyte globulin after
90 owed by a second TBI and RLI, rejected their marrow graft without rejecting their transplanted kidney
91 f CD4 cells from an HLA-mismatched unrelated marrow graft would substantially reduce the risk of grad
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