白细胞介素15
免疫学
白血病
生物
人性化鼠标
单克隆抗体
醛类白血病
癌症研究
T细胞
医学
抗体
白细胞介素
细胞因子
免疫系统
作者
Thomas A. Waldmann,Kevin C. Conlon,Dawn Stewart,TatYana A. Worthy,John E. Janik,Thomas A. Fleisher,Paul S. Albert,William D. Figg,Shawn D. Spencer,Mark Raffeld,J M Decker,Carolyn K. Goldman,Bonita R. Bryant,Michael Petrus,Stephen P. Creekmore,John C. Morris
出处
期刊:Blood
[American Society of Hematology]
日期:2013-01-17
卷期号:121 (3): 476-484
被引量:67
标识
DOI:10.1182/blood-2012-08-450585
摘要
Abstract In the present study, Hu-Mikβ1, a humanized mAb directed at the shared IL-2/IL-15Rβ subunit (CD122) was evaluated in patients with T-cell large granular lymphocytic (T-LGL) leukemia. Hu-Mikβ1 blocked the trans presentation of IL-15 to T cells expressing IL-2/IL-15Rβ and the common γ-chain (CD132), but did not block IL-15 action in cells that expressed the heterotrimeric IL-15 receptor in cis. There was no significant toxicity associated with Hu-Mikβ1 administration in patients with T-LGL leukemia, but no major clinical responses were observed. One patient who had previously received murine Mikβ1 developed a measurable Ab response to the infused Ab. Nevertheless, the safety profile of this first in-human study of the humanized mAb to IL-2/IL-15Rβ (CD122) supports its evaluation in disorders such as refractory celiac disease, in which IL-15 and its receptor have been proposed to play a critical role in the pathogenesis and maintenance of disease activity. The protocol is registered with www.clinicaltrials.gov as number NCT 00076180.
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