Atorvastatin Reduces Plasma Levels of Chemokine (CXCL10) in Patients with Crohn's Disease

被引:58
作者
Grip, Olof
Janciauskiene, Sabina
机构
[1] Division of Gastroenterology and Hepatology, Department of Clinical Sciences Malmö, Lund University, Malmö
[2] Chronic Inflammatory and Degenerative Diseases Research Unit, Department of Clinical Sciences Malmö, Lund University, Malmö
关键词
D O I
10.1371/journal.pone.0005263
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: In Crohn's disease high tissue expression and serum levels of chemokines and their receptors are known to correlate with disease activity. Because statins can reduce chemokine expression in patients with coronary diseases, we wanted to test whether this can be achieved in patients with Crohn's disease. Methodology/Principal Findings: We investigated plasma levels of chemokines (CCL2, CCL4, CCL11, CCL13, CCL17, CCL22, CCL26, CXCL8, CXCL10) and endothelial cytokines (sP-selectin, sE-selectin, sICAM-3, thrombomodulin) in ten Crohn's disease patients before and after thirteen weeks' daily treatment with 80 mg atorvastatin. Of the 13 substances investigated, only CXCL10 was found to be significantly reduced (by 34%, p = 0.026) in all of the treated patients. Levels of CXCL10 correlated with C-reactive protein (r = 0.82, p<0.01). Conclusions/Significance: CXCL10 is a ligand for the CXCR3 receptor, the activation of which results in the recruitment of T lymphocytes and the perpetuation of mucosal inflammation. Hence the reduction of plasma CXCL10 levels by atorvastatin may represent a candidate for an approach to the treatment of Crohns disease in the future.
引用
收藏
页数:6
相关论文
共 52 条
[1]   Effect of statin therapy on C-reactive protein levels - The Pravastatin Inflammation/CRP Evaluation (PRINCE): A randomized trial and cohort study [J].
Albert, MA ;
Danielson, E ;
Rifai, N ;
Ridker, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (01) :64-70
[2]   Chemokine: Receptor structure, interactions, and antagonism [J].
Allen, Samantha J. ;
Crown, Susan E. ;
Handel, Tracy M. .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :787-820
[3]   Elevated circulating platelet-derived microparticles in patients with active inflammatory bowel disease [J].
Andoh, A ;
Tsujikawa, T ;
Hata, K ;
Araki, Y ;
Kitoh, K ;
Sasaki, M ;
Yoshida, T ;
Fujiyama, Y .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (09) :2042-2048
[4]   Chemokines and leukocyte traffic [J].
Baggiolini, M .
NATURE, 1998, 392 (6676) :565-568
[5]   Chemokine expression in IBD. Mucosal chemokine expression is unselectively increased in both ulcerative colitis and Crohn's disease [J].
Banks, C ;
Bateman, A ;
Payne, R ;
Johnson, P ;
Sheron, N .
JOURNAL OF PATHOLOGY, 2003, 199 (01) :28-35
[6]   Nuclear factor kappa B [J].
Barnes, PJ .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1997, 29 (06) :867-870
[7]   Gastroenterology 1 - Inflammatory bowel disease: cause and immunobiology [J].
Baumgart, Daniel C. ;
Carding, Simon R. .
LANCET, 2007, 369 (9573) :1627-1640
[8]   Elevated ICAM-1 and MCP-1 plasma levels in subjects at high cardiovascular risk are diminished by atorvastatin treatment.: Atorvastatin on inflammatory markers study:: A substudy of achieve cholesterol targets fast with atorvastatin stratified titration [J].
Blanco-Colio, Luis Miguel ;
Martin-Ventura, Jose Luis ;
de Teresa, Eduardo ;
Farsang, Csaba ;
Gaw, Allan ;
Gensini, GianFranco ;
Leiter, Lawrence A. ;
Langer, Anatoly ;
Martineau, Pierre ;
Egido, Jesus .
AMERICAN HEART JOURNAL, 2007, 153 (05) :881-888
[9]   The effect of atorvastatin treatment on lipid profile and adhesion molecule levels in hypercholesterolemic patients: Relation to low-density lipoprotein receptor gene polymorphism [J].
Bolewski, Andrzej ;
Lipiecki, Janusz ;
Plewa, Robert ;
Burchardt, Pawel ;
Siminiak, Tomasz .
CARDIOLOGY, 2008, 111 (02) :140-146
[10]   Dbl and the Rho GTPases activate NFκB by IκB kinase (IKK)-dependent and IKK-independent pathways [J].
Cammarano, MS ;
Minden, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (28) :25876-25882