Methotrexate-how does it really work?

被引:320
作者
Chan, Edwin S. L. [1 ]
Cronstein, Bruce N. [1 ]
机构
[1] NYU, Sch Med, Dept Med, New York, NY 10016 USA
关键词
RHEUMATOID-ARTHRITIS PATIENTS; PERIPHERAL-BLOOD MONOCYTES; A(2B) RECEPTOR ACTIVATION; T-CELLS; MONONUCLEAR-CELLS; ADENOSINE RELEASE; MEDIATOR RELEASE; CLINICAL STATUS; FOLINIC ACID; IN-VIVO;
D O I
10.1038/nrrheum.2010.5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Methotrexate remains a cornerstone in the treatment of rheumatoid arthritis and other rheumatic diseases. Folate antagonism is known to contribute to the antiproliferative effects that are important in the action of methotrexate against malignant diseases, but concomitant administration of folic or folinic acid does not diminish the anti-inflammatory potential of this agent, which suggests that other mechanisms of action might be operative. Although no single mechanism is sufficient to account for all the anti-inflammatory activities of methotrexate, the release of adenosine from cells has been demonstrated both in vitro and in vivo. Methotrexate might also confer anti-inflammatory properties through the inhibition of polyamines. The biological effects on inflammation associated with adenosine release have provided insight into how methotrexate exerts its effects against inflammatory diseases and at the same time causes some of its well-known adverse effects. These activities contribute to the complex and multifaceted mechanisms that make methotrexate efficacious in the treatment of inflammatory disorders.
引用
收藏
页码:175 / 178
页数:4
相关论文
共 37 条
  • [1] AFANE M, 1989, CLIN EXP RHEUMATOL, V7, P603
  • [2] ALARCON GS, 1990, ARTHRITIS RHEUM-US, V33, P1156
  • [3] Chan ESL, 2006, BRIT J PHARMACOL, V148, P1144, DOI 10.1038/sj.bjp.0706812
  • [4] ADENOSINE - A PHYSIOLOGICAL MODULATOR OF SUPEROXIDE ANION GENERATION BY HUMAN-NEUTROPHILS
    CRONSTEIN, BN
    KRAMER, SB
    WEISSMANN, G
    HIRSCHHORN, R
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 158 (04) : 1160 - 1177
  • [5] Low-dose methotrexate: A mainstay in the treatment of rheumatoid arthritis
    Cronstein, BN
    [J]. PHARMACOLOGICAL REVIEWS, 2005, 57 (02) : 163 - 172
  • [6] THE ANTIINFLAMMATORY MECHANISM OF METHOTREXATE - INCREASED ADENOSINE RELEASE AT INFLAMED SITES DIMINISHES LEUKOCYTE ACCUMULATION IN AN IN-VIVO MODEL OF INFLAMMATION
    CRONSTEIN, BN
    NAIME, D
    OSTAD, E
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) : 2675 - 2682
  • [7] CRONSTEIN BN, 1992, J IMMUNOL, V148, P2201
  • [8] Adenosine generation catalyzed by CD39 and CD73 expressed on regulatory T cells mediates immune suppression
    Deaglio, Silvia
    Dwyer, Karen M.
    Gao, Wenda
    Friedman, David
    Usheva, Anny
    Erat, Anna
    Chen, Jiang-Fan
    Enjyoji, Keiichii
    Linden, Joel
    Oukka, Mohamed
    Kuchroo, Vijay K.
    Strom, Terry B.
    Robson, Simon C.
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (06) : 1257 - 1265
  • [9] Pharmacogenetic and metabolite measurements are associated with clinical status in patients with rheumatoid arthritis treated with methotrexate: results of a multicentred cross sectional observational study
    Dervieux, T
    Furst, D
    Lein, DO
    Capps, R
    Smith, K
    Caldwell, J
    Kremer, J
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (08) : 1180 - 1185
  • [10] EFFECT OF ANTIARTHRITIC DRUGS ON THE ENHANCED INTERLEUKIN-1 (IL-1) PRODUCTION BY MACROPHAGES FROM ADJUVANT-INDUCED ARTHRITIC (AA) RATS
    DIMARTINO, MJ
    JOHNSON, WJ
    VOTTA, B
    HANNA, N
    [J]. AGENTS AND ACTIONS, 1987, 21 (3-4): : 348 - 350