Increased CXCL8 (IL-8) expression in multiple sclerosis

被引:111
作者
Lund, BT
Ashikian, N
Ta, HQ
Chakryan, Y
Manoukian, K
Groshen, S
Gilmore, W
Cheema, GS
Stohl, W
Burnett, ME
Ko, D
Kachuck, NJ
Weiner, LP
机构
[1] Univ So Calif, Keck Sch Med, Dept Neurol, Los Angeles, CA 90033 USA
[2] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA 90033 USA
[3] Univ So Calif, Keck Sch Med, Dept Cell & Neurobiol, Los Angeles, CA 90033 USA
[4] Univ So Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
[5] Univ So Calif, Los Angeles Cty Med Ctr, Keck Sch Med, Dept Med,Div Rheumatol, Los Angeles, CA 90033 USA
关键词
multiple sclerosis; inflammation; CXCL8; interferon-beta; 1a; monocytes;
D O I
10.1016/j.jneuroim.2004.06.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple Sclerosis (MS) is a chronic inflammatory disease of the CNS which is characterized by large mononuclear cell infiltration and significant demyelination. CXCL8 is a chemo-attractant for both neutrophils and monocytes and triggers their firm adhesion to endothelium. In this study, we demonstrate that serum CXCL8 and CXCL8 secretion from PBMCs are significantly higher in untreated MS patients compared to controls and are significantly reduced in MS patients receiving interferon-beta1a therapy. We suggest that CXCL8 may serve as a marker of monocyte activity in MS and may play a role in monocyte recruitment to the CNS. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:161 / 171
页数:11
相关论文
共 101 条
[1]   Mechanisms involved in Helicobacter pylori-induced interleukin-8 production by a gastric cancer cell line, MKN45 [J].
Aihara, M ;
Tsuchimoto, D ;
Takizawa, H ;
Azuma, A ;
Wakebe, H ;
Ohmoto, Y ;
Imagawa, K ;
Kikuchi, M ;
Mukaida, N ;
Matsushima, K .
INFECTION AND IMMUNITY, 1997, 65 (08) :3218-3224
[2]   T-CELLS RESPONSIVE TO MYELIN BASIC-PROTEIN IN PATIENTS WITH MULTIPLE-SCLEROSIS [J].
ALLEGRETTA, M ;
NICKLAS, JA ;
SRIRAM, S ;
ALBERTINI, RJ .
SCIENCE, 1990, 247 (4943) :718-721
[3]   CXC chemokines generate age-related increases in neutrophil-mediated brain inflammation and blood-brain barrier breakdown [J].
Anthony, D ;
Dempster, R ;
Fearn, S ;
Clements, J ;
Wells, G ;
Perry, VH ;
Walker, K .
CURRENT BIOLOGY, 1998, 8 (16) :923-926
[4]   Chemokines in the CNS: plurifunctional mediators in diverse states [J].
Asensio, VC ;
Campbell, IL .
TRENDS IN NEUROSCIENCES, 1999, 22 (11) :504-512
[5]   Chemokines and their receptors in neurobiology: perspectives in physiology and homeostasis [J].
Bacon, KB ;
Harrison, JK .
JOURNAL OF NEUROIMMUNOLOGY, 2000, 104 (01) :92-97
[6]  
BAGGIOLINI M, 1994, ADV IMMUNOL, V55, P97
[7]   INTERLEUKIN-8 AND THE CHEMOKINE FAMILY [J].
BAGGIOLINI, M ;
LOETSCHER, P ;
MOSER, B .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1995, 17 (02) :103-108
[8]   Presentation of αB-crystallin to T cells in active multiple sclerosis lesions:: An early event following inflammatory demyelination [J].
Bajramovic, JJ ;
Plomp, AC ;
van der Goes, A ;
Koevoets, C ;
Newcombe, J ;
Cuzner, ML ;
van Noort, JM .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :4359-4366
[9]   Transcriptional analysis of multiple sclerosis brain lesions reveals a complex pattern of cytokine expression [J].
Baranzini, SE ;
Elfstrom, C ;
Chang, SY ;
Butunoi, C ;
Murray, R ;
Higuchi, R ;
Oksenberg, JR .
JOURNAL OF IMMUNOLOGY, 2000, 165 (11) :6576-6582
[10]   A leukocyte homologue of the IL-8 receptor CXCR-2 mediates the accumulation of macrophages in atherosclerotic lesions of LDL receptor-deficient mice [J].
Boisvert, WA ;
Santiago, R ;
Curtiss, LK ;
Terkeltaub, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) :353-363