Evaluation of the biological activities of the IL-15 superagonist complex, ALT-803, following intravenous versus subcutaneous administration in murine models

被引:31
作者
Liu, Bai [1 ]
Jones, Monica [1 ]
Kong, Lin [1 ]
Noel, Terra [1 ]
Jeng, Emily K. [1 ]
Shi, Sixiang [3 ,4 ]
England, Christopher G. [3 ,4 ]
Alter, Sarah [1 ]
Miller, Jeffrey S. [2 ]
Cai, Weibo [3 ,4 ]
Rhode, Peter R. [1 ]
Wong, Hing C. [1 ]
机构
[1] Altor BioSci, 2810 North Commerce Pkwy, Miramar, FL 33025 USA
[2] Univ Minnesota, Masonic Canc Ctr, Div Hematol Oncol & Transplantat, Minneapolis, MN USA
[3] Univ Wisconsin, Dept Radiol, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Med Phys, 1530 Med Sci Ctr, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
Interleukin-15; Interleukin-15R alpha; ALT-803; CD8 T cells; NK cells; Immunotherapy; CD8(+) T-CELLS; MULTIPLE-MYELOMA; INTERLEUKIN-15; THERAPY; FUSION;
D O I
10.1016/j.cyto.2017.12.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ALT-803 is a fusion protein complex consisting of an interleukin (IL)-15 superagonist and a dimeric IL-15 receptor alpha sushi domain IgG1 Fc fusion protein. When administered to mice, ALT-803 is capable of inducing natural killer (NK) and CD8(+) T cell proliferation and activation, and effectively promoting potent anti-tumor responses. Currently, ALT-803 is in clinical trials for treatment of various solid tumors and hematological malignancies. In the initial phase of these clinical studies, intravenous (iv) injection was used according to the route used in pre-clinical efficacy studies. In order to evaluate the possible advantage of subcutaneous (sc) injection versus iv injection, this study compared the biological activity of the two treatment regimens of ALT-803 in pre-clinical in vivo models. The pharmacokinetics, immune stimulation, and anti-tumor efficacy of iv and sc injection routes of ALT-803 in C57BL/6 mice were compared. The half-life of ALT-803 was 7.5 h for iv versus 7.7 h for sc with the maximal detected serum concentration of ALT-803 to be 3926 ng/ml at 0.5 h time-point following iv injection versus 495 ng/ml at 16 h post sc injection. Biodistribution studies indicated that sc ALT-803, similarly to iv ALT-803 as previously reported, has a greater tissue distribution and longer residence time in lymphoid tissues compared to recombinant IL-15. Notably, ALT-803 when administered either iv or sc induced comparable proliferation and activation of CD8(+) T and NK cells and resulted in similar reductions of tumor burden. A toxicity study of mice receiving multiple injections of ALT-803 for 4 weeks by iv or sc routes revealed equivalent immune-related changes. The gradual absorbance into the blood stream and lower maximal blood levels of ALT-803 in sc-injected mice, along with similar anti-tumor efficacy support the administration of ALT-803 by sc injection in patients with various malignancies and infectious diseases.
引用
收藏
页码:105 / 112
页数:8
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