The Use of Biologic Therapies in the Treatment of Rheumatoid Arthritis

被引:31
作者
Wang, Dashan [1 ]
Li, Yan [2 ]
Liu, Yuan [2 ]
Shi, Guixiu [2 ]
机构
[1] Shandong Med Coll, Mol Biol Res Ctr, Linyi 276000, Shandong, Peoples R China
[2] Xiamen Univ, Dept Rheumatol & Clin Immunol, Affiliated Hosp 1, Xiamen 361003, Fujian, Peoples R China
关键词
Biologic therapy; cell-targeted therapy; cytokine-targeted therapy; rheumatoid arthritis; DOUBLE-BLIND; INADEQUATE RESPONSE; PHASE-II; MONOCLONAL-ANTIBODY; CERTOLIZUMAB PEGOL; CLINICAL-EFFICACY; T-CELLS; SAFETY; METHOTREXATE; PATHOGENESIS;
D O I
10.2174/138920101506140910150612
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The use of biologic agents has revolutionized the management of rheumatoid arthritis (RA) in the past two decades. These biologic agents directly target molecules and cells involved in the pathogenesis of RA. Biologic agents indeed lead to a better prognosis and clinical remission in patients with RA, especially in patients who are not well-controlled with traditional disease-modifying anti-rheumatic drugs (DMARDs). Currently, five TNF inhibitors (infliximab, etanercept, adalimumab, golimumab and certolizumab pegol), an IL-6 receptor antagonist (tocilizumab), an IL-1 receptor antagonist (anakinra), a B cell depleting agent (rituximab) and a T cell co-stimulation inhibitor (abatacept) have been approved for the treatment of RA. With the increased understanding of the pathogenic mechanisms of RA and advantages in manufacturing biotechnology of pharmaceutical companies, a series of novel biologic therapeutic approaches are being developed. In the present paper, we will summarize the biologic agents currently available to treat RA, and the prospective biologic therapies that might be used in the management of RA in future.
引用
收藏
页码:542 / 548
页数:7
相关论文
共 101 条
[1]
Mechanisms of CTLA-4-Ig in tolerance induction [J].
Alegre, ML ;
Fallarino, F .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (02) :149-160
[2]
Alldred A, 2001, Expert Opin Pharmacother, V2, P1137, DOI 10.1517/14656566.2.7.1137
[3]
Effector T cells in rheumatoid arthritis: Lessons from animal models [J].
Alzabin, Saba ;
Williams, Richard O. .
FEBS LETTERS, 2011, 585 (23) :3649-3659
[4]
Switching rheumatoid arthritis treatments: An update [J].
Atzeni, Fabiola ;
Sarzi-Puttini, Piercarlo ;
Gorla, Roberto ;
Marchesoni, Antonio ;
Caporali, Roberto .
AUTOIMMUNITY REVIEWS, 2011, 10 (07) :397-403
[5]
Th17 Cells in Immunopathogenesis and treatment of rheumatoid arthritis [J].
Azizi, Gholamreza ;
Jadidi-Niaragh, Farhad ;
Mirshafiey, Abbas .
INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, 2013, 16 (03) :243-253
[6]
Bingham CO, 2002, J RHEUMATOL, V29, P3
[7]
Blumenauer B, 2002, COCHRANE DB SYST REV, V2002, DOI DOI 10.1002/14651858.CD003785
[8]
Understanding emerging treatment paradigms in rheumatoid arthritis [J].
Breedveld, Ferdinand C. ;
Combe, Bernard .
ARTHRITIS RESEARCH & THERAPY, 2011, 13
[9]
Emerging cell and cytokine targets in rheumatoid arthritis [J].
Burmester, Gerd R. ;
Feist, Eugen ;
Doerner, Thomas .
NATURE REVIEWS RHEUMATOLOGY, 2014, 10 (02) :77-88
[10]
Efficacy and safety of mavrilimumab in subjects with rheumatoid arthritis [J].
Burmester, Gerd R. ;
Weinblatt, Michael E. ;
McInnes, Iain B. ;
Porter, Duncan ;
Barbarash, Olga ;
Vatutin, Mykola ;
Szombati, Istvan ;
Esfandiari, Ehsanollah ;
Sleeman, Matthew A. ;
Kane, Christopher D. ;
Cavet, Guy ;
Wang, Bing ;
Godwood, Alex ;
Magrini, Fabio .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (09) :1445-1452