Infliximab in severe steroid-refractory ulcerative colitis: A pilot study

被引:0
作者
Kaser, A
Mairinger, T
Vogel, W
Tilg, H
机构
[1] Univ Innsbruck Hosp, Dept Med, Div Gastroenterol & Hepatol, A-6020 Innsbruck, Austria
[2] Univ Innsbruck Hosp, Dept Pathol, A-6020 Innsbruck, Austria
关键词
ulcerative colitis; TNF alpha; inflammatory bowel disease; infliximab;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tumor necrosis factor-alpha (TNF alpha)-neutralization by infliximab has previously proven efficacious in chronic active Crohn's disease (CD). We performed an open-label pilot study of a single infusion of 5 mg/kg infliximab in six patients with severe active, steroid-refractory ulcerative colitis (UC). Clinical activity was evaluated according to Lichtiger on days -1, day 7, and day 28. Colonoscopy with biopsy was performed on day -1 and day 7. All patients showed marked clinical improvement by day 7 (Lichtiger score 16.3 +/- 0.4 [day -1] vs 4.8 +/- 0.7 [day 7], P < 0.0001). Four of six patients had long-term remission (Lichtiger score 7.7 +/- 2.2 [day 28], P < 0.01 compared to day -1), with a median follow-up of 5.5 months. Colonoscopy confirmed significant healing of endoscopic lesions. The inflammatory infiltrate disappeared on H&E stains, with a marked reduction in infiltrating neutrophils. Semiquantitative evaluation of T and B lymphocytes and macrophages by immunohistochemistry did not reveal major differences compared to pre-treatment. Apoptotic cells in the mucosa were reduced on day 7. Our data point toward a novel efficacious treatment option in severe steroid-refractory UC and raise the need for controlled trials.
引用
收藏
页码:930 / 933
页数:4
相关论文
共 12 条
[1]   Tumor necrosis factor α antibody (infliximab) therapy profoundly down-regulates the inflammation in Crohn's ileocolitis [J].
Baert, FJ ;
D'Haens, GR ;
Peeters, M ;
Hiele, MI ;
Schaible, TF ;
Shealy, D ;
Geboes, K ;
Rutgeerts, PJ .
GASTROENTEROLOGY, 1999, 116 (01) :22-28
[2]   Measurement of in vivo rectal mucosal cytokine and eicosanoid production in ulcerative colitis using filter paper [J].
Carty, E ;
De Brabander, M ;
Feakins, RM ;
Rampton, DS .
GUT, 2000, 46 (04) :487-492
[3]   Infliximab for patients with refractory ulcerative colitis [J].
Chey, WY .
INFLAMMATORY BOWEL DISEASES, 2001, 7 :S30-S33
[4]   Infliximab for refractory ulcerative colitis [J].
Chey, WY ;
Hussain, A ;
Ryan, C ;
Potter, GD ;
Shah, A .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2001, 96 (08) :2373-2381
[5]   Inflammatory bowel disease: Etiology and pathogenesis [J].
Fiocchi, C .
GASTROENTEROLOGY, 1998, 115 (01) :182-205
[6]   CONSTRUCTION AND INITIAL CHARACTERIZATION OF A MOUSE-HUMAN CHIMERIC ANTI-TNF ANTIBODY [J].
KNIGHT, DM ;
TRINH, H ;
LE, JM ;
SIEGEL, S ;
SHEALY, D ;
MCDONOUGH, M ;
SCALLON, B ;
MOORE, MA ;
VILCEK, J ;
DADDONA, P ;
GHRAYEB, J .
MOLECULAR IMMUNOLOGY, 1993, 30 (16) :1443-1453
[7]   CYCLOSPORINE IN SEVERE ULCERATIVE-COLITIS REFRACTORY TO STEROID-THERAPY [J].
LICHTIGER, S ;
PRESENT, DH ;
KORNBLUTH, A ;
GELERNT, I ;
BAUER, J ;
GALLER, G ;
MICHELASSI, F ;
HANAUER, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (26) :1841-1845
[8]   CROHNS DISEASE (REGIONAL ENTERITIS) OF THE LARGE INTESTINE AND ITS DISTINCTION FROM ULCERATIVE COLITIS [J].
LOCKHARTMUMMERY, HE ;
MORSON, BC .
GUT, 1960, 1 (02) :87-105
[9]   Crohn's disease in Olmsted County, Minnesota, 1940-1993: Incidence, prevalence, and survival [J].
Loftus, EV ;
Silverstein, MD ;
Sandborn, WJ ;
Tremaine, WJ ;
Harmsen, WS ;
Zinsmeister, AR .
GASTROENTEROLOGY, 1998, 114 (06) :1161-1168
[10]   Mechanisms in failure of infliximab for Crohn's disease [J].
Nikolaus, S ;
Raedler, A ;
Kühbacher, T ;
Sfikas, N ;
Fölsch, UR ;
Schreiber, S .
LANCET, 2000, 356 (9240) :1475-1479