Novel immunosuppressant agents targeting activated lymphocytes by biocompatible MPC polymer conjugated with interleukin-2

被引:12
作者
Chiba, N.
Ueda, M.
Shimada, T.
Jinno, H.
Watanabe, J.
Ishihara, K.
Kitajima, M.
机构
[1] Keio Univ, Sch Med, Dept Surg, Shinjuku Ku, Tokyo 1608582, Japan
[2] Univ Tokyo, Sch Engn, Dept Mat Engn, Tokyo, Japan
关键词
MPC polymer; immunosuppressive agents; interleukin-2; receptor; high affinity;
D O I
10.1159/000099598
中图分类号
R61 [外科手术学];
学科分类号
摘要
The immunopharmacological profile of novel biocompatible water-soluble interleukin-2 (IL-2)-conjugated 2-methacryloyloxyethyl phosphorylcholine (MPC) polymer immunosuppressive agents was established. MPC-co-n butyl methacrylate ( BMA)-co-p-nitrophenylcarbonyloxyethyl methacrylate (NPMA) ( PMBN) was prepared as a backbone for these novel agents. PMBN contained MPC as a biocompatible unit, BMA as a hydrophobic domain in water, and NPMA as an immobilizable unit with IL-2. This research showed that proliferation of cell lines with high-affinity IL-2 receptors derived from T cell malignancies were suppressed by the PMBN conjugated with IL-2 (PMBN-IL2 conjugate) incorporating paclitaxel (PTX) and cyclosporin A at lower concentrations than used conventionally. PMBN-IL2 conjugates incorporating PTX also inhibited the proliferation of responder cells in a human mixed lymphocyte culture at a lower concentration than unconjugated drug. However, PMBN-IL2 conjugates incorporating FK506 inhibited proliferation no more than FK506 alone. The PMBN-IL2 conjugate with PTX may therefore be useful for selectively eliminating activated lymphocytes that hyperproduce high-affinity IL-2 receptors. As an entirely human 'immunotoxin analogue' it may not be associated with the dose-limiting toxicity and immunogenicity of conventional immunotoxins. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:103 / 110
页数:8
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