A novel anti-inflammatory role for simvastatin in inflammatory arthritis

被引:356
作者
Leung, BP
Sattar, N
Crilly, A
Prach, M
McCarey, DW
Payne, H
Madhok, R
Campbell, C
Gracie, JA
Liew, FY
McInnes, IB
机构
[1] Univ Glasgow, Glasgow Royal Infirm, Dept Pathol Biochem, Glasgow G31 2ER, Lanark, Scotland
[2] Univ Glasgow, Glasgow Royal Infirm, Dept Immunol, Glasgow G31 2ER, Lanark, Scotland
[3] Univ Glasgow, Glasgow Royal Infirm, Ctr Rheumat Dis, Glasgow G31 2ER, Lanark, Scotland
关键词
D O I
10.4049/jimmunol.170.3.1524
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
3-Hydroxy-3-methylglutaryl-CoA reductase inhibitors (statins) exert favorable effects on lipoprotein metabolism, but may also possess anti-inflammatory properties. Therefore, we explored the activities of simvastatin, a lipophilic statin, in a Th1-driven model of murine inflammatory arthritis. We report in this study that simvastatin markedly inhibited not only developing but also clinically evident collagen-induced arthritis in doses that were unable to significantly alter cholesterol concentrations in vivo. Ex vivo analysis demonstrated significant suppression of collagen-specific Th1 Immoral and cellular immune responses. Moreover, simvastatin reduced anti-CD3/anti-CD28 proliferation and IFN-gamma release from mononuclear cells derived from peripheral blood and synovial fluid. Proinflammatory cytokine production in vitro by T cell contact-activated macrophages was suppressed by simvastatin, suggesting that such observations have direct clinical relevance. These data clearly illustrate the therapeutic potential of statin-sensitive pathways in inflammatory arthritis. The Journal of Immunology, 2003, 170: 1524-1530.
引用
收藏
页码:1524 / 1530
页数:7
相关论文
共 35 条
[1]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[2]  
Chabaud M, 1999, ARTHRITIS RHEUM-US, V42, P963, DOI 10.1002/1529-0131(199905)42:5<963::AID-ANR15>3.0.CO
[3]  
2-E
[4]  
Davignon J, 2001, ANN ENDOCRINOL-PARIS, V62, P101
[5]   HMG-CoA reductase inhibitors (statins) increase endothelial progenitor cells via the PI 3-kinase/Akt pathway [J].
Dimmeler, S ;
Aicher, A ;
Vasa, M ;
Mildner-Rihm, C ;
Adler, K ;
Tiemann, M ;
Rütten, H ;
Fichtlscherer, S ;
Martin, H ;
Zeiher, AM .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (03) :391-397
[6]   Shift toward T lymphocytes with a T helper 1 cytokine-secretion profile in the joints of patients with rheumatoid arthritis [J].
Dolhain, RJEM ;
vanderHeiden, AN ;
terHaar, NT ;
Breedveld, FC ;
Miltenburg, AMM .
ARTHRITIS AND RHEUMATISM, 1996, 39 (12) :1961-1969
[7]   Anti-TNFα therapy of rheumatoid arthritis:: what have we learned? [J].
Feldmann, M ;
Maini, RN .
ANNUAL REVIEW OF IMMUNOLOGY, 2001, 19 :163-196
[8]   Role of cytokines in rheumatoid arthritis [J].
Feldmann, M ;
Brennan, FM ;
Maini, RN .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :397-440
[9]  
Freeman DJ, 2001, CIRCULATION, V103, P357
[10]   Apolipoprotein A-I inhibits the production of interleukin-1β and tumor necrosis factor-α by blocking contact-mediated activation of monocytes by T lymphocytes [J].
Hyka, N ;
Dayer, JM ;
Modoux, C ;
Kohno, T ;
Edwards, CK ;
Roux-Lombard, P ;
Burger, D .
BLOOD, 2001, 97 (08) :2381-2389