A review of the action of tacrolimus (FK506) on experimental models of rheumatoid arthritis

被引:52
作者
Miyata, S [1 ]
Ohkubo, Y [1 ]
Mutoh, S [1 ]
机构
[1] Fujisawa Pharmaceut Co Ltd, Med Biol Res Labs, Yodogawa Ku, Osaka 5328514, Japan
关键词
tacrolimus; DMARD; rheumatoid arthritis; adjuvant-induced arthritis; collagen-induced arthritis;
D O I
10.1007/s00011-004-1318-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tacrolimus (FK506) is an immunosuppressive drug, widely used for organ transplantation and atopic dermatitis. Tacrolimus exerts its immuno suppressive effects primarily by interfering with the activation of T cells, via inhibition of calcineurin. Recent clinical studies have also demonstrated the efficacy of tacrolimus in the treatment of rheumatoid arthritis (RA), an autoimmune disease in which T cells play a pivotal role in pathogenesis. Inflammatory cytokines such as TNF-alpha, IL-1beta, and IL-6 are involved in development of the disease. Recently, modes of action of tacrolimus on RA have been intensively studied in in vitro and animal arthritis models, demonstrating that tacrolimus exerts various novel actions as an anti-rheumatic drug. The pharmacological action of tacrolimus suggests that it has potential to specifically suppress the production of pathogenic inflammatory cytokines with a low frequency of infection, improve joint inflammation and bone/cartilage destruction. fully recover loss of functional status, exert rapid relief in arthritic pain, and promote osteogenic and chondrogenic differentiation. Here we review the action of tacrolimus on experimental models of RA, with a focus on our recent studies, and provide further insight into experimental models used for identifying efficacious anti-rheumatic drugs.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 89 条
[31]   LPS induction of gene expression in human monocytes [J].
Guha, M ;
Mackman, N .
CELLULAR SIGNALLING, 2001, 13 (02) :85-94
[32]   Functional disability and quality-of-life assessment in clinical practice [J].
Guillemin, F .
RHEUMATOLOGY, 2000, 39 :17-23
[33]   Pancytopenia secondary to methotrexate therapy in rheumatoid arthritis [J].
GutierrezUrena, S ;
Molina, JF ;
Garcia, CO ;
Cuellar, ML ;
Espinoza, LR .
ARTHRITIS AND RHEUMATISM, 1996, 39 (02) :272-276
[34]   THE EFFECTS OF ANTIINFLAMMATORY AND ANTIALLERGIC DRUGS ON CYTOKINE RELEASE AFTER STIMULATION OF HUMAN WHOLE-BLOOD BY LIPOPOLYSACCHARIDE AND ZYMOSAN A [J].
HARTMAN, DA ;
OCHALSKI, SJ ;
CARLSON, RP .
INFLAMMATION RESEARCH, 1995, 44 (07) :269-274
[35]   COX-2 inhibitors [J].
Hawkey, CJ .
LANCET, 1999, 353 (9149) :307-314
[36]   FUNCTIONAL ASSESSMENT OF THE HAND - REPRODUCIBILITY, ACCEPTABILITY, AND UTILITY OF A NEW SYSTEM FOR MEASURING STRENGTH [J].
HELLIWELL, P ;
HOWE, A ;
WRIGHT, V .
ANNALS OF THE RHEUMATIC DISEASES, 1987, 46 (03) :203-208
[37]   The mechanism of action of cyclosporin A and FK506 [J].
Ho, S ;
Clipstone, N ;
Timmermann, L ;
Northrop, J ;
Graef, I ;
Fiorentino, D ;
Nourse, J ;
Crabtree, GR .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1996, 80 (03) :S40-S45
[38]   IMMUNOSUPPRESSIVE EFFECT OF FK506 ON COLLAGEN-INDUCED ARTHRITIS IN RATS [J].
INAMURA, N ;
HASHIMOTO, M ;
NAKAHARA, K ;
AOKI, H ;
YAMAGUCHI, I ;
KOHSAKA, M .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1988, 46 (01) :82-90
[39]   Stem cells for repair of cartilage and bone: the next challenge in osteoarthritis and rheumatoid arthritis [J].
Jorgensen, C ;
Noel, D ;
Apparailly, F ;
Sany, J .
ANNALS OF THE RHEUMATIC DISEASES, 2001, 60 (04) :305-309
[40]  
Kalden JR, 2001, J RHEUMATOL, V28, P1983