Rheumatoid arthritis: An overview of new and emerging therapies

被引:124
作者
Doan, T [1 ]
Massarotti, E [1 ]
机构
[1] Tufts Univ New England Med Ctr, Boston, MA USA
关键词
rheumatoid arthritis; biological therapies; cytokines;
D O I
10.1177/0091270005277938
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Rheumatoid arthritis (RA) is a chronic, inflammatory, systemic autoimmune disorder characterized by symmetric inflammation of synovial joints leading to progressive erosion of cartilage and bone. The aim of treatment is to mitigate joint destruction, preserve function, and prevent disability. The American College of Rheumatology guidelines for the treatment of RA recommend that newly diagnosed patients with RA begin treatment with disease-modifying antirheumatic drugs (DMARDs) within 3 months of diagnosis. Methotrexate remains the most commonly prescribed DMARD and is the standard by which recent new and emerging therapies are measured. Increasing knowledge regarding the immunologic basis of RA and advances in biotechnology have resulted in new, targeted biological therapies against proinflammatory cytokines that have dramatically changed the treatment paradigm and outcomes of patients with RA. This article reviews the pharmacological rationale underlying RA therapy, with a focus on currently available biological therapies and new therapies in development. (c) 2005 the American College of Clinical Pharmacology.
引用
收藏
页码:751 / 762
页数:12
相关论文
共 113 条
[1]  
*ABB LAB, HUM AD PACK INS
[2]  
Afeltra A., 2001, Current Drug Targets - Immune Endocrine and Metabolic Disorders, V1, P45, DOI 10.2174/1568008013341677
[3]   WEEKLY PULSE METHOTREXATE IN RHEUMATOID-ARTHRITIS - CLINICAL AND IMMUNOLOGICAL EFFECTS IN A RANDOMIZED, DOUBLE-BLIND-STUDY [J].
ANDERSEN, PA ;
WEST, SG ;
ODELL, JR ;
VIA, CS ;
CLAYPOOL, RG ;
KOTZIN, BL .
ANNALS OF INTERNAL MEDICINE, 1985, 103 (04) :489-496
[4]  
[Anonymous], 2000, Cochrane Database Syst Rev, DOI DOI 10.1002/14651858.CD002048
[5]  
[Anonymous], COCHRANE DATABASE SY
[6]   Long term effectiveness of antimalarial drugs in rheumatic diseases [J].
Aviña-Zubieta, JA ;
Galindo-Rodriguez, G ;
Newman, S ;
Suarez-Almazor, ME ;
Russell, AS .
ANNALS OF THE RHEUMATIC DISEASES, 1998, 57 (10) :582-587
[7]   Disease activity and risk of lymphoma in patients with rheumatoid arthritis:: nested case-control study [J].
Baecklund, E ;
Ekbom, A ;
Sparén, P ;
Feltelius, N ;
Klareskog, L .
BRITISH MEDICAL JOURNAL, 1998, 317 (7152) :180-181
[8]   A comparison of etanercept and methotrexate in patients with early rheumatoid arthritis [J].
Bathon, JM ;
Martin, RW ;
Fleischmann, RM ;
Tesser, JR ;
Schiff, MH ;
Keystone, EC ;
Genovese, MC ;
Wasko, MC ;
Moreland, LW ;
Weaver, AL ;
Markenson, J ;
Finck, BK .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (22) :1586-1593
[9]  
Bensen W, 1999, CLIN EXP RHEUMATOL, V17, pS95
[10]  
Bijlsma Johannes W. J., 2002, Trends in Immunology, V23, P59, DOI 10.1016/S1471-4906(01)02128-7