Strategies for chemokine antagonists as therapeutics

被引:84
作者
Proudfoot, AEI [1 ]
Power, CA [1 ]
Rommel, C [1 ]
Wells, TNC [1 ]
机构
[1] Serono Pharmaceut Res Inst, CH-1228 Geneva, Switzerland
关键词
chemokine; chemokine receptors; inflammation; HIV; glycosaminoglycan; signaling; receptor trafficking;
D O I
10.1016/S1044-5323(02)00128-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemokines are responsible for specific recruitment of leukocytes that are involved both in homing as well as in inflammation. Dysregulation of the system results in excessive recruitment to inflammatory sites and thus prevention of this recruitment is an effective anti-inflammatory strategy. Chemokine receptors are not limited only to cellular recruitment but are also the essential co-factor along with CD4 that enable HIV-1 viruses to infect cells. In this review we discuss the various points of intervention that can be addressed to provide anti-inflammatory and anti-HIV infectivity therapeutics. These include prevention of the receptor-ligand interaction, prevention of the chemokine-glycosaminoglycan interaction, interfering with the signaling pathways that are induced upon receptor activation, and modification of receptor trafficking pathways. We summarize the status of the approaches that have been undertaken to produce therapeutics that block chemokine action. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:57 / 65
页数:9
相关论文
共 64 条
  • [1] The chemokine RANTES is a crucial mediator of the progression from acute to chronic colitis in the rat
    Ajuebor, MN
    Hogaboam, GM
    Kunkel, SL
    Proudfoot, AEI
    Wallace, JL
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 166 (01) : 552 - 558
  • [2] A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity
    Baba, M
    Nishimura, O
    Kanzaki, N
    Okamoto, M
    Sawada, H
    Iizawa, Y
    Shiraishi, M
    Aramaki, Y
    Okonogi, K
    Ogawa, Y
    Meguro, K
    Fujino, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) : 5698 - 5703
  • [3] Blanpain C, 2001, J LEUKOCYTE BIOL, V69, P977
  • [4] Decreased lesion formation in CCR2-/- mice reveals a role for chemokines in the initiation of atherosclerosis
    Boring, L
    Gosling, J
    Cleary, M
    Charo, IF
    [J]. NATURE, 1998, 394 (6696) : 894 - 897
  • [5] Aberrant in vivo T helper type 2 cell response and impaired eosinophil recruitment in CC chemokine receptor 8 knockout mice
    Chensue, SW
    Lukacs, NW
    Yang, TY
    Shang, XZ
    Frait, KA
    Kunkel, SL
    Kung, T
    Wiekowski, MT
    Hedrick, JA
    Cook, DN
    Zingoni, A
    Narula, SK
    Zlotnik, A
    Barrat, FJ
    O'Garra, A
    Napolitano, M
    Lira, SA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (05) : 573 - 584
  • [6] Role of Rac in controlling the actin cytoskeleton and chemotaxis in motile cells
    Chung, CY
    Lee, S
    Briscoe, C
    Ellsworth, C
    Firtel, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) : 5225 - 5230
  • [7] A key role for CC chemokine receptor 4 in lipopolysaccharide-induced endotoxic shock
    Chvatchko, Y
    Hoogewerf, AJ
    Meyer, A
    Alouani, S
    Juillard, P
    Buser, R
    Conquet, F
    Proudfoot, AEI
    Wells, TNC
    Power, CA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (10) : 1755 - 1763
  • [8] CLARKLEWIS I, 1991, J BIOL CHEM, V266, P23128
  • [9] Randomized phase-II study of BB-10010 (macrophage inflammatory protein-1α) in patients with advanced breast cancer receiving 5-fluorouracil, adriamycin, and cyclophosphamide chemotherapy
    Clemons, MJ
    Marshall, E
    Dürig, J
    Watanabe, K
    Howell, A
    Miles, D
    Earl, H
    Kiernan, J
    Griffiths, A
    Towlson, K
    DeTakats, P
    Testa, NG
    Dougal, M
    Hunter, MG
    Wood, LM
    Czaplewski, LG
    Millar, A
    Dexter, TM
    Lord, BI
    [J]. BLOOD, 1998, 92 (05) : 1532 - 1540
  • [10] Human interferon-inducible 10-kDa protein and human interferon-inducible T cell α chemoattractant are allotopic ligands for human CXCR3:: Differential binding to receptor states
    Cox, MA
    Jenh, CH
    Gonsiorek, W
    Fine, J
    Narula, SK
    Zavodny, PJ
    Hipkin, RW
    [J]. MOLECULAR PHARMACOLOGY, 2001, 59 (04) : 707 - 715