Efficacy of the anti-TNF-α antibody infliximab against refractory systemic vasculitides:: an open pilot study on 10 patients

被引:214
作者
Bartolucci, P [1 ]
Ramanoelina, J [1 ]
Cohen, P [1 ]
Mahr, A [1 ]
Godmer, P [1 ]
Le Hello, C [1 ]
Guillevin, L [1 ]
机构
[1] Assistance Publ Hop Paris, Hop Avicenne, UPRES Rech Clin & Therapeut, French Vasculitis Study Grp,Dept Internal Med, F-93000 Bobigny, France
关键词
D O I
10.1093/rheumatology/41.10.1126
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Evidence indicates that tumour necrosis factor (TNF) is a major agent in the pathogenesis of vasculitis. We studied the short-term effect of anti-TNF-alpha antibody in systemic vasculitis patients refractory to steroids and immunosuppressive agents. Methods. Ten patients refractory to corticosteroids and at least one immunosuppressant and who had persistently active disease or a new flare were included. Seven had Wegener's granulomatosis, two had rheumatoid arthritis-associated vasculitis and one had cryoglobulinaemia with mean duration of 9.1, 21.5 and 17 yr. They received infliximab (5 mg/kg) on days 1, 14, 42 and then every 8 weeks. Immunosuppressants were stopped between days 0 and 42 for eight patients, while the steroid dose was maintained or lowered. The treatment response was evaluated clinically with the Birmingham Vasculitis Activity Score 2000 (BVAS). Results. Complete or partial remission was observed in all patients. The mean BVAS at entry was 9.1 (range 4-15) and had declined to 1.9 (range 0-4) by day 42 and 1.3 (range 0-4) at 6 months; BVAS of 0 was recorded for four patients on day 42 and for five at 6 months. The only adverse effect was cutaneous eruption in two patients. Conclusion. Anti-TNF-alpha successfully induced prompt symptomatic responses in patients with systemic vasculitis not responding to conventional treatment. Infliximab was well tolerated during the short-term follow-up.
引用
收藏
页码:1126 / 1132
页数:7
相关论文
共 19 条
  • [1] Tumor necrosis factor α antibody (infliximab) therapy profoundly down-regulates the inflammation in Crohn's ileocolitis
    Baert, FJ
    D'Haens, GR
    Peeters, M
    Hiele, MI
    Schaible, TF
    Shealy, D
    Geboes, K
    Rutgeerts, PJ
    [J]. GASTROENTEROLOGY, 1999, 116 (01) : 22 - 28
  • [2] Brandt J, 2000, ARTHRITIS RHEUM-US, V43, P1346, DOI 10.1002/1529-0131(200006)43:6<1346::AID-ANR18>3.0.CO
  • [3] 2-E
  • [4] CSERNOK E, 1994, CLIN EXP IMMUNOL, V95, P244
  • [5] DEGUCHI Y, 1990, CLIN EXP IMMUNOL, V81, P311
  • [6] Gayraud M, 2001, ARTHRITIS RHEUM, V44, P666, DOI 10.1002/1529-0131(200103)44:3<666::AID-ANR116>3.0.CO
  • [7] 2-A
  • [8] WEGENER GRANULOMATOSIS - AN ANALYSIS OF 158 PATIENTS
    HOFFMAN, GS
    KERR, GS
    LEAVITT, RY
    HALLAHAN, CW
    LEBOVICS, RS
    TRAVIS, WD
    ROTTEM, M
    FAUCI, AS
    [J]. ANNALS OF INTERNAL MEDICINE, 1992, 116 (06) : 488 - 498
  • [9] NOMENCLATURE OF SYSTEMIC VASCULITIDES - PROPOSAL OF AN INTERNATIONAL CONSENSUS CONFERENCE
    JENNETTE, JC
    FALK, RJ
    ANDRASSY, K
    BACON, PA
    CHURG, J
    GROSS, WL
    HAGEN, EC
    HOFFMAN, GS
    HUNDER, GG
    KALLENBERG, CGM
    MCCLUSKEY, RT
    SINICO, RA
    REES, AJ
    VANES, LA
    WALDHERR, R
    WIIK, A
    [J]. ARTHRITIS AND RHEUMATISM, 1994, 37 (02): : 187 - 192
  • [10] THE AMERICAN-COLLEGE-OF-RHEUMATOLOGY 1990 CRITERIA FOR THE CLASSIFICATION OF WEGENER GRANULOMATOSIS
    LEAVITT, RY
    FAUCI, AS
    BLOCH, DA
    MICHEL, BA
    HUNDER, GG
    AREND, WP
    CALABRESE, LH
    FRIES, JF
    LIE, JT
    LIGHTFOOT, RW
    MASI, AT
    MCSHANE, DJ
    MILLS, JA
    STEVENS, MB
    WALLACE, SL
    ZVAIFLER, NJ
    [J]. ARTHRITIS AND RHEUMATISM, 1990, 33 (08): : 1101 - 1107