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1 (e.g. CD30 and CD52), and immunotoxins (e.g. denileukin diftitox).
2 g cells are depleted after multiple doses of denileukin diftitox.
3 NM) stage, histologic grade, and response to denileukin diftitox.
4 e susceptibility of T-cell leukemia cells to denileukin diftitox.
6 ses of bexarotene (75 mg/day-300 mg/day) and denileukin diftitox (18 mcg/kg per day x 3 days every 21
8 of two dose levels (9 or 18 microg/kg/d) of denileukin diftitox administered 5 consecutive days ever
10 results demonstrate that the combination of denileukin diftitox and bexarotene is well tolerated and
11 toxin conjugate DAB(389)IL-2 (also known as denileukin diftitox and ONTAK) is capable of enhancing t
15 he efficacy, safety, and pharmacokinetics of denileukin diftitox (DAB389IL-2, Ontak [Ligand Pharmaceu
18 estigate efficacy and safety of two doses of denileukin diftitox (DD; DAB(389)-interleukin-2 [IL-2]),
20 ted that a CD25(high) targeting immunotoxin (denileukin diftitox) depleted FoxP3(+) Treg cells, decre
22 to evaluate the efficacy and tolerability of denileukin diftitox for relapsed or refractory B-cell NH
23 sure enhanced susceptibility of the cells to denileukin diftitox fusion toxin-targeting and -intoxica
25 0% of the 71 patients with CTCL treated with denileukin diftitox had an objective response (20% parti
26 knowledge we report for the first time that denileukin diftitox has also dramatic effects regarding
28 ected therapies, including the fusion toxin, denileukin diftitox, histone deacetylase inhibitors, and
29 depleted with the IL-2-toxin fusion protein (denileukin diftitox), HIV-1 infection is significantly i
32 compartments and (2) the dose scheduling of denileukin diftitox in combination with a recombinant po
35 performed in vivo Treg depletion with Ontak (denileukin diftitox) in two SIVsab-infected controller m
41 abetes, we demonstrate that the injection of denileukin diftitox leads to a dramatic development of t
43 une responses, (3) the lack of inhibition by denileukin diftitox of host immune responses directed ag
44 In this study, we examined (1) the effect of denileukin diftitox on the deletion of Treg cells in var
45 murine model (1) the differential effects of denileukin diftitox on Treg cells in different cellular
50 nd combination with the IL-2 toxin conjugate denileukin diftitox resulted in more than additive toxic
52 cells in the tumor grafts were depleted with denileukin diftitox, suggesting that tumor-specific T ce
53 after a single intraperitoneal injection of denileukin diftitox; the reduction was evident within 24
59 and (4) the importance of dose scheduling of denileukin diftitox when used in combination with a vacc
60 compartments, (2) the advantage of combining denileukin diftitox with a vaccine to enhance antigen-sp
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