Maintenance of remission in Crohn's disease current and emerging therapeutic options

被引:25
作者
Brookes, MJ [1 ]
Green, JRB [1 ]
机构
[1] City Gen Hosp, Dept Gastroenterol, Stoke On Trent ST4 6QG, Staffs, England
关键词
D O I
10.2165/00003495-200464100-00004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Crohn's disease is a chronic inflammatory bowel disorder with a relapsing and remitting course. Once remission is achieved, the main aim of the management of Crohn's disease is maintenance of that remission. Significant advances have been made into understanding the aetiology and pathogenesis of inflammatory bowel disease. With these advances in understanding come increasing numbers of new agents and therapies, aimed both at active disease and the subsequent maintenance of remission in Crohn's disease. Current therapeutic strategies in maintaining remission in Crohn's disease include 5-aminosalicylates (e.g. sulfasalazine, mesalazine), thiopurines (e.g. azathioprine, 6-mercaptopurine [mercaptopurine]), methotrexate and infliximab. The 5-ammosalicylates appear to have efficacy limited to either surgically induced remission and/or limited small bowel Crohn's disease. The immunomodulators now have an established role in Crohn's maintenance. Azathioprine and 6-mercaptopurine are effective in chronic active disease and corticosteroid-dependant Crohn's disease. Methotrexate hits similar indications, although it appears to be an alternative in patients who are intolerant of, or resistant to, the thiopurines. The most recent breakthrough has been in the field of biological therapy for maintenance of remission in Crohn's disease. Treatment of patients with the anti-tumour necrosis factor (TNF)-alpha antibody infliximab has been shown already to be effective in inducing remission. Recent studies have now confirmed a role for infliximab in delaying relapse and maintaining remission in patients responsive to infliximab induction therapy. However, results with soluble TNFalpha receptors have been disappointing. A number of other biological and nonbiological agents have shown potential, though trials of the 'newer' biological agents have thus far been disappointing, in the maintenance of remission in Crohn's disease. The evidence for theses agents is currently limited, in many cases to treating active disease; however, these data are discussed in this article in order to provide an overview of future potential therapies. The aim of this review is to provide clinicians with an insight into current and emerging therapeutic agents for the maintenance of remission of Crohn's disease.
引用
收藏
页码:1069 / 1089
页数:21
相关论文
共 161 条
[131]   Control of intestinal inflammation by regulatory T cells [J].
Singh, B ;
Read, S ;
Asseman, C ;
Malmström, V ;
Mottet, C ;
Stephens, LA ;
Stepankova, R ;
Tlaskalova, H ;
Powrie, F .
IMMUNOLOGICAL REVIEWS, 2001, 182 :190-200
[132]   A preliminary study of growth hormone therapy for Crohn's disease [J].
Slonim, AE ;
Bulone, L ;
Damore, MB ;
Goldberg, T ;
Wingertzahn, MA ;
McKinley, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (22) :1633-1637
[133]   A PHARMACOGENETIC BASIS FOR THE SAFE AND EFFECTIVE USE OF AZATHIOPRINE AND OTHER THIOPURINE DRUGS IN DERMATOLOGICAL PATIENTS [J].
SNOW, JL ;
GIBSON, LE .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1995, 32 (01) :114-116
[134]   THE ROLE OF GENETIC-VARIATION IN THIOPURINE METHYLTRANSFERASE ACTIVITY AND THE EFFICACY AND/OR SIDE-EFFECTS OF AZATHIOPRINE THERAPY IN DERMATOLOGICAL PATIENTS [J].
SNOW, JL ;
GIBSON, LE .
ARCHIVES OF DERMATOLOGY, 1995, 131 (02) :193-197
[135]   Randomised controlled trial of CDP571 antibody to tumour necrosis factor-alpha in Crohn's disease [J].
Stack, WA ;
Mann, SD ;
Roy, AJ ;
Heath, P ;
Sopwith, M ;
Freeman, J ;
Holmes, G ;
Long, R ;
Forbes, A ;
Kamm, MA ;
Hawkey, CJ .
LANCET, 1997, 349 (9051) :521-524
[136]  
STEINHART AH, 2001, COCHRANE DATABASE SY, V1
[137]  
STRANGE EF, 1995, GASTROENTEROLOGY, V109, P774
[138]  
STUCK AE, 1989, REV INFECT DIS, V11, P954
[139]  
Subhani JM, 1998, ALIMENT PHARM THERAP, V12, P1039
[140]  
SUMMERS RW, 1979, GASTROENTEROLOGY, V77, P847