Tocilizumab inhibits signal transduction mediated by both mIL-6R and sIL-6R, but not by the receptors of other members of IL-6 cytokine family

被引:283
作者
Mihara, M [1 ]
Kasutani, K [1 ]
Okazaki, M [1 ]
Nakamura, A [1 ]
Kawai, S [1 ]
Sugimoto, M [1 ]
Matsumoto, Y [1 ]
Ohsugi, Y [1 ]
机构
[1] Chugai Pharmaceut Co Ltd, Fuji Gotemba Res Labs, Shizuoka 4128513, Japan
关键词
tocilizumab; IL-6; receptor; IL-6 family cytokine;
D O I
10.1016/j.intimp.2005.05.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
To characterize the biological activity of tocilizumab, a humanized anti-human interleukin-6 receptor (IL-6R) monoclonal antibody, we examined its binding activity to both soluble IL-6R (sIL-6R) and membrane bound IL-6R (mIL-6R) and its neutralizing activity to other IL-6 family cytokines. ELISA assay demonstrated that tocilizumab bound to sIL-6R and inhibited IL-6 binding to sIL-6R in a dose-dependent manner. The dissociation constant (Kd value) for IL-6R was determined to be 2.54 +/- 0.12 nmol/L by Scatchard analysis. In addition, tocilizumab had the ability to dissociate IL-6 and sIL-6R from their preformed complex. The immune complex of tocilizumab and sIL-6R did not transmit signaling. Moreover, tocilizumab suppressed the IL-6/sIL-6R complex-induced proliferation of human gp130-transfected cell, BAF-h130. In addition, tocilizumab had the ability to bind to human IL-6R expressing COS-7 cells and to suppress the growth of the IL-6-dependent myeloma cell line, KPMM2. Finally, to analyze the specificity of this antibody, the effects on signal transduction of IL-6 family cytokines such as interleukin-11 (IL-11), oncostatin M (OSM), leukemia inhibitory factor (LIF), and ciliary neurotrophic factor (CNTF) were examined using murine transfectant cell lines (BaF/IL-6R, BaF/IL-11R, BaF/OSMR, BaF/LIFR and BaF/CNTFR) that proliferate depending on IL-6, IL-11, OSM, LIF and human CNTF, respectively. Tocilizumab inhibited the proliferation of BaF/IL-6R induced by IL-6, but did not inhibit the proliferation of BaF/IL-11R,BaF/OSMR, BaF/LIFR and BaF/CNTFR cells induced by their corresponding cytokines. These lines of evidence indicate that tocilizumab is able to bind to both sIL-6R and mIL-6R and to inhibit IL-6 binding to its receptors, leading to the blockade of the IL-6 signaling through both sIL-6R and mIL-6R, but not block the signaling of other IL-6 family cytokines. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1731 / 1740
页数:10
相关论文
共 16 条
[1]
INTERLEUKIN-6 IN BIOLOGY AND MEDICINE [J].
AKIRA, S ;
TAGA, T ;
KISHIMOTO, T .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :1-78
[2]
GOTO H, 1995, LEUKEMIA, V9, P711
[3]
MOLECULAR-CLONING AND EXPRESSION OF AN IL-6 SIGNAL TRANSDUCER, GP130 [J].
HIBI, M ;
MURAKAMI, M ;
SAITO, M ;
HIRANO, T ;
TAGA, T ;
KISHIMOTO, T .
CELL, 1990, 63 (06) :1149-1157
[4]
HIRATA Y, 1989, J IMMUNOL, V143, P2900
[5]
A pilot randomized trial of a human anti-interleukin-6 receptor monoclonal antibody in active Crohn's disease [J].
Ito, H ;
Takazoe, M ;
Fukuda, Y ;
Hibi, T ;
Kusugami, K ;
Andoh, A ;
Matsumoto, T ;
Yamamura, T ;
Azuma, J ;
Nishimoto, N ;
Yoshizaki, K ;
Shimoyama, T ;
Kishimoto, T .
GASTROENTEROLOGY, 2004, 126 (04) :989-996
[6]
INTERLEUKIN-6 FAMILY OF CYTOKINES AND GP130 [J].
KISHIMOTO, T ;
AKIRA, S ;
NARAZAKI, M ;
TAGA, T .
BLOOD, 1995, 86 (04) :1243-1254
[7]
Treatment of rheumatoid arthritis with humanized anti-interleukin-6 receptor antibody - A multicenter, double-blind, placebo-controlled trial [J].
Nishimoto, N ;
Yoshizaki, K ;
Miyasaka, N ;
Yamamoto, K ;
Kawai, S ;
Takeuchi, T ;
Hashimoto, J ;
Azuma, J ;
Kishimoto, T .
ARTHRITIS AND RHEUMATISM, 2004, 50 (06) :1761-1769
[8]
Improvement In Castleman's disease by humanized anti-interleukin-6 receptor antibody therapy [J].
Nishimoto, N ;
Sasai, M ;
Shima, Y ;
Nakagawa, M ;
Matsumoto, T ;
Shirai, T ;
Kishimoto, T ;
Yoshizaki, K .
BLOOD, 2000, 95 (01) :56-61
[9]
OKUNO Y, 1992, EXP HEMATOL, V20, P395
[10]
ROSEJOHN S, 1991, J BIOL CHEM, V266, P3841