A T-cell-selective interleukin 2 mutein exhibits potent antitumor activity and is well tolerated in vivo

被引:117
作者
Shanafelt, AB
Lin, Y
Shanafelt, MC
Forte, CP
Dubois-Stringfellow, N
Carter, C
Gibbons, JA
Cheng, SI
Delaria, KA
Fleischer, R
Greve, JM
Gundel, R
Harris, K
Kelly, R
Koh, B
Li, Y
Lantz, L
Mak, P
Neyer, L
Plym, MJ
Roczniak, S
Serban, D
Thrift, J
Tsuchiyama, L
Wetzel, M
Wong, M
Zolotorev, A
机构
[1] Bayer Corp, Div Pharmaceut, Res Sci, Biotechnol, Berkeley, CA 94701 USA
[2] Bayer Corp, Div Pharmaceut, Proc Sci, Biotechnol, Berkeley, CA 94701 USA
[3] Bayer Corp, Div Pharmaceut, Dept Canc & Osteoporosis Res, W Haven, CT 06556 USA
关键词
structure-function analysis; mutagenesis; pharmacology; cancer; receptor;
D O I
10.1038/81199
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Human interleukin 2 (IL-2; Proleukin) is an approved therapeutic for advanced-stage metastatic cancer; however, its use is restricted because of severe systemic toxicity. Its function as a central mediator of T-cell activation may contribute to its efficacy for cancer therapy. However, activation of natural killer (NK) cells by therapeutically administered IL-2 may mediate toxicity. Here we have used targeted mutagenesis of human IL-2 to generate a mutein with similar to3,000-fold in vitro selectivity for T cells over NK cells relative to wild-type IL-2, We compared the variant, termed BAY 50-4798, with human IL-2 (Proleukin) in a therapeutic dosing regimen in chimpanzees, and found that although the T-cell mobilization and activation properties of BAY 50-4788 were comparable to human IL-2, BAY 50-4798 was better tolerated in the chimpanzee. BAY 50-4798 was also shown to inhibit metastasis in a mouse tumor model. These results indicate that BAY 50-4798 may exhibit a greater therapeutic index than IL-2 in humans in the treatment of cancer and AIDS.
引用
收藏
页码:1197 / 1202
页数:6
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