Identification of a CXCR4 antagonist, a T140 analog, as an anti-rheumatoid arthritis agent

被引:128
作者
Tamamura, H [1 ]
Fujisawa, M
Hiramatsu, K
Mizumoto, M
Nakashima, H
Yamamoto, N
Otaka, A
Fujii, N
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
[2] Takeda Chem Ind Ltd, Div Pharmaceut Res, Yodogawa Ku, Osaka 5328686, Japan
[3] St Marianna Univ, Sch Med, Miyamae Ku, Kawasaki, Kanagawa 2168511, Japan
[4] Tokyo Med & Dent Univ, Sch Med, Bunkyo Ku, Tokyo 1138519, Japan
来源
FEBS LETTERS | 2004年 / 569卷 / 1-3期
关键词
CXCR4; antagonist; rheumatoid arthritis; T140; collagen-induced arthritis; delayed-type hypersensitivity;
D O I
10.1016/j.febslet.2004.05.056
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
Several recent papers support the involvement of an interaction between stromal cell-derived factor-1 (SDF-1/ CXCL12) and its receptor, chemokine receptor CXCR4, in memory T cell migration in the inflamed rheumatoid arthritis (RA) synovium. Analogs of the 14-mer peptide T140 were previously found to be specific CXCR4 antagonists that were characterized as not only HIV-entry inhibitors but also anticancer-metastatic agents. In this study, a T140 analog, 4F-benzoyl-TN14003, was proven to inhibit CXCL12-mediated migration of human Jurkat cells and mouse splenocyte in a dose-dependent manner in vitro (IC50 = 0.65 and 0.54 nM, respectively). Furthermore, slow release administration by subcutaneous injection (s.c.) of 4F-benzoyl-TN14003 using an Alzet osmotic pump significantly suppressed the delayed-type hypersensitivity response induced by sheep red blood cells in mice, and significantly ameliorated clinical severity in collagen-induced arthritis in mice. As such, T140 analogs might be attractive lead compounds for chemotherapy of RA. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:99 / 104
页数:6
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