Treatment of rheumatoid arthritis by selective inhibition of T-cell activation with fusion protein CTLA4Ig

被引:832
作者
Kremer, JM
Westhovens, R
Leon, M
Di Giorgio, E
Alten, R
Steinfeld, S
Russell, A
Dougados, M
Emery, P
Nuamah, IF
Williams, GR
Becker, JC
Hagerty, DT
Moreland, LW
机构
[1] Ctr Rheumatol, Albany, NY 12206 USA
[2] Univ Ziekenhuizen Leuven, Dept Rheumatol, Louvain, Belgium
[3] Free Univ Brussels, Ctr Hosp Univ Ambroise Pare, Mons, Belgium
[4] Ctr Enfermedades Reumat, Quilmes, Argentina
[5] Schlosspk Klin, Dept Rheumatol, Berlin, Germany
[6] Erasme Univ Hosp, Dept Rheumatol, B-1070 Brussels, Belgium
[7] Univ Alberta Hosp, Edmonton, AB T6G 2B7, Canada
[8] Univ Paris 05, Hop Cochin, Assistance Publ Hop Paris, Paris, France
[9] Leeds Gen Infirm, Dept Rheumatol, Leeds, W Yorkshire, England
[10] Bristol Myers Squibb Co, Pharmaceut Res Inst, Princeton, NJ 08543 USA
[11] Univ Alabama, Sch Med, Dept Med, Birmingham, AL USA
关键词
D O I
10.1056/NEJMoa035075
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Effective new therapies are needed for rheumatoid arthritis. Current therapies target the products of activated macrophages; however, T cells also have an important role in rheumatoid arthritis. A fusion protein- cytotoxic T-lymphocyte-associated antigen 4-IgG1 (CTLA4Ig)-is the first in a new class of drugs known as costimulation blockers being evaluated for the treatment of rheumatoid arthritis. CTLA4Ig binds to CD80 and CD86 on antigen-presenting cells, blocking the engagement of CD28 on T cells and preventing T-cell activation. A preliminary study showed that CTLA4Ig may be effective for the treatment of rheumatoid arthritis. Methods: We randomly assigned patients with active rheumatoid arthritis despite methotrexate therapy to receive 2 mg of CTLA4Ig per kilogram of body weight (105 patients), 10 mg of CTLA4Ig per kilogram (115 patients), or placebo (119 patients) for six months. All patients also received methotrexate therapy during the study. The clinical response was assessed at six months with use of the criteria of the American College of Rheumatology (ACR), which define the response according to its extent: 20 percent (ACR 20), 50 percent (ACR 50), or 70 percent (ACR 70). Additional end points included measures of the health-related quality of life. Results: Patients treated with 10 mg of CTLA4Ig per kilogram were more likely to have an ACR 20 than were patients who received placebo (60 percent vs. 35 percent, P<0.001). Significantly higher rates of ACR 50 and ACR 70 responses were seen in both CTLA4Ig groups than in the placebo group. The group given 10 mg of CTLA4Ig per kilogram had clinically meaningful and statistically significant improvements in all eight subscales of the Medical Outcomes 36-Item Short-Form General Health Survey. CTLA4Ig was well tolerated, with an overall safety profile similar to that of placebo. Conclusions: In patients with active rheumatoid arthritis who were receiving methotrexate, treatment with CTLA4Ig significantly improved the signs and symptoms of rheumatoid arthritis and the health-related quality of life. CTLA4Ig is a promising new therapy for rheumatoid arthritis.
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收藏
页码:1907 / 1915
页数:9
相关论文
共 47 条
  • [1] Balsa A, 1996, BRIT J RHEUMATOL, V35, P33
  • [2] A comparison of etanercept and methotrexate in patients with early rheumatoid arthritis
    Bathon, JM
    Martin, RW
    Fleischmann, RM
    Tesser, JR
    Schiff, MH
    Keystone, EC
    Genovese, MC
    Wasko, MC
    Moreland, LW
    Weaver, AL
    Markenson, J
    Finck, BK
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (22) : 1586 - 1593
  • [3] Bathon JM, 2001, NEW ENGL J MED, V344, P240
  • [4] Bathon JM, 2001, NEW ENGL J MED, V344, P76
  • [5] Bresnihan B, 1998, ARTHRITIS RHEUM, V41, P2196, DOI 10.1002/1529-0131(199812)41:12<2196::AID-ART15>3.0.CO
  • [6] 2-2
  • [7] PHENOTYPIC ANALYSIS OF SYNOVIAL TISSUE AND PERIPHERAL-BLOOD LYMPHOCYTES ISOLATED FROM PATIENTS WITH RHEUMATOID-ARTHRITIS
    CUSH, JJ
    LIPSKY, PE
    [J]. ARTHRITIS AND RHEUMATISM, 1988, 31 (10): : 1230 - 1238
  • [8] THE COMPARATIVE EFFICACY AND TOXICITY OF 2ND-LINE DRUGS IN RHEUMATOID-ARTHRITIS - RESULTS OF 2 METAANALYSES
    FELSON, DT
    ANDERSON, JJ
    MEENAN, RF
    [J]. ARTHRITIS AND RHEUMATISM, 1990, 33 (10): : 1449 - 1461
  • [9] FINCK B, 1994, SCIENCE, V256, P1225
  • [10] The clinical features of rheumatoid arthritis
    Grassi, W
    De Angelis, R
    Lamanna, G
    Cervini, C
    [J]. EUROPEAN JOURNAL OF RADIOLOGY, 1998, 27 : S18 - S24