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1 nventional induction therapy (basiliximab or rabbit antithymocyte globulin).
2 bortezomib, methylprednisone, rituximab, and rabbit antithymocyte globulin.
3 and either 20 mg alemtuzumab or 6 mg per kg rabbit antithymocyte globulin.
4 lymphoid irradiation, cyclophosphamide, and rabbit-antithymocyte globulin.
5 after successful induction therapy using two rabbit antithymocyte globulins.
6 one were randomly assigned to receive either rabbit antithymocyte globulin (1.5 mg per kilogram of bo
8 no donor-specific antibodies [DSA]) received rabbit antithymocyte globulin (2 x 1.5 mg/kg, postoperat
9 zumab (one dose of 30 mg, in 70 patients) or rabbit antithymocyte globulin (a total of 6 mg per kilog
10 imed at assessing the efficacy and safety of rabbit antithymocyte globulin and infliximab induction i
11 plant recipients who received induction with rabbit antithymocyte globulin and rituximab and initiate
12 nonmyeloablative conditioning protocol with rabbit-antithymocyte globulin and low-dose total lymphoi
14 The addition of low, nondepleting doses of rabbit antithymocyte globulin (ATG) to human peripheral
15 transplant total lymphoid irradiation (TLI), rabbit antithymocyte globulin (ATG), and a single donor
16 and 2022 and compared the risk of PTLD with rabbit antithymocyte globulin (ATG), basiliximab, and al
18 poside, cytarabine, and melphalan as well as rabbit antithymocyte globulin before autologous HCT.
19 ey transplant recipients who were prescribed rabbit antithymocyte globulin, calcineurin inhibitor, my
20 steroid elimination at 1 week, and combined rabbit antithymocyte globulin/daclizumab induction, prev
21 ts suggests that the use of a single 3 mg/kg rabbit antithymocyte globulin dose followed by EVR combi
23 acrolimus, everolimus (EVR), and prednisone (rabbit antithymocyte globulin/EVR, n = 85); basiliximab,
25 We therefore tested T-cell depletion with rabbit antithymocyte globulin followed by sirolimus mono
27 phylactic CMVIG and induction with high-dose rabbit antithymocyte globulin (>10 mg/kg) were associate
29 ts required steroid therapy and one required rabbit antithymocyte globulin in addition to MMF and ste
31 on maintenance prednisone in the setting of rabbit antithymocyte globulin induction and tacrolimus a
32 der-drained PAK (n=47) transplants receiving rabbit antithymocyte globulin induction from June 1998 t
33 n early corticosteroid withdrawal regimen of rabbit antithymocyte globulin induction, tacrolimus, and
34 n early corticosteroid withdrawal regimen of rabbit antithymocyte globulin induction, tacrolimus, myc
36 The patient received methylprednisolone and rabbit antithymocyte globulin intravenously during scalp
38 is with CMVIG and appropriate induction with rabbit antithymocyte globulin may be important to reduce
39 recipient pretreatment with a single dose of rabbit antithymocyte globulin or alemtuzumab and posttra
40 late mofetil were required as well as either rabbit antithymocyte globulin or interleukin-2 receptor
41 ain immunosuppressive regimens that included rabbit antithymocyte globulin or tacrolimus/mycophenolat
42 cyclophosphamide, and 6.5 mg/kg intravenous rabbit antithymocyte globulin or to receive 1.0 g/m(2) i
43 alemtuzumab (versus no induction, anti-CD25, rabbit antithymocyte globulin, or rabbit antithymocyte g
44 ction categories: no-induction, alemtuzumab, rabbit antithymocyte globulin (r-ATG), and interleukin-2
45 ne were randomized for 3 different regimens: rabbit antithymocyte globulin (r-ATG)/EVR (N = 85); basi
46 Recipients were grouped by induction type: rabbit antithymocyte globulin (r-ATG, n = 688) and human
47 to December 2008 who received induction with rabbit-antithymocyte globulin (r-ATG), alemtuzumab, or a
48 stics, we generated 1:1 pairs of alemtuzumab-rabbit antithymocyte globulin (rATG) (5330 pairs) and ba
49 Patients were treated with T cell-depleting rabbit antithymocyte globulin (rATG) (6 mg/kg, n = 17) o
50 when alemtuzumab induction was compared with rabbit antithymocyte globulin (rATG) (Thymoglobulin [Gen
51 ing strategies have not been established for rabbit antithymocyte globulin (rATG) after heart transpl
56 ne the safety and efficacy of induction with rabbit antithymocyte globulin (RATG) compared with inter
59 71 patients who received either steroids or rabbit antithymocyte globulin (RATG) for orthotopic live
60 adult recipients who received rituximab and rabbit antithymocyte globulin (rATG) in combination as i
61 teroid-free immunosuppression protocol using rabbit antithymocyte globulin (RATG) induction in orthot
64 discharge, we developed a protocol to extend rabbit antithymocyte globulin (rATG) induction therapy i
65 imus 1.5 mg versus MMF in patients receiving rabbit antithymocyte globulin (rATG) induction, mainly d
66 nt centers comparing a control group of with rabbit antithymocyte globulin (rATG) induction, rapid st
68 Delaying CNI initiation by using induction rabbit antithymocyte globulin (rATG) may provide kidneys
69 ients, who were randomized to receive either rabbit antithymocyte globulin (RATG) or steroids as indu
70 bsets were evaluated before and after adding rabbit antithymocyte globulin (rATG) to mixed lymphocyte
71 mparing single-dose (SD) versus divided-dose rabbit antithymocyte globulin (rATG), and a maintenance
73 ace, human leukocyte antigen (HLA) mismatch, rabbit antithymocyte globulin (RATG), interleukin-2 rece
74 ostatic proliferation by Ki-67(+) T cells in rabbit antithymocyte globulin (rATG)-treated patients th
76 tients exposed (4.23%) versus not exposed to rabbit antithymocyte globulin (rATG; 0.53%; P=0.019) or
77 n basiliximab (1998), daclizumab (1998), and rabbit antithymocyte globulin (rATG; 1999) replaced anti
78 the prognostic influence of induction type: rabbit antithymocyte globulin (rATG; 2 mg/kg x 5)/rituxi
79 tablished to assess clinical experience with rabbit antithymocyte globulin (rATG; Thymoglobulin) in l
81 e thousand consecutive LT patients receiving rabbit antithymocyte globulin+/-rituximab induction were
83 anti-CD25, rabbit antithymocyte globulin, or rabbit antithymocyte globulin/rituximab) induction (P =
84 nosuppression was Tac-Pred based in nine and rabbit antithymocyte globulin-Tac based in six cases.
85 e-ITx was carried out under Tac-Pred in six, rabbit antithymocyte globulin-Tac in eight, and alemtuzu
86 ndomized to receive a single 3-mg/kg dose of rabbit antithymocyte globulin, tacrolimus, everolimus (E
88 d pretreatment with approximately 5 mg/kg of rabbit antithymocyte globulin (Thymoglobulin) in the hou
89 a randomized, international study comparing rabbit antithymocyte globulin (TMG) and basiliximab (BAS
90 tients with Aspergillus colonization, use of rabbit antithymocyte globulin was associated with 4-fold
91 lation using busulfan, cyclophosphamide, and rabbit antithymocyte globulin was followed by aHSCT.
92 ox-proportional hazard model, treatment with rabbit antithymocyte globulin was significantly associat