Leukocyte Adsorptive Apheresis for the Treatment of Active Ulcerative Colitis: A Prospective, Uncontrolled, Pilot Study

被引:173
作者
Hanai, Hiroyuki [1 ]
Watanabe, Fumitoshi [2 ]
Takeuchi, Ken [3 ]
Iida, Takayuki [3 ]
Yamada, Masami [4 ]
Iwaoka, Yasushi [4 ]
Saniabadi, Abby [5 ]
Matsushita, Isao [6 ]
Sato, Yoshihiko [6 ]
Tozawa, Kotaro [1 ]
Arai, Hajime [7 ]
Furuta, Takahisa [7 ]
Sugimoto, Ken [7 ]
Bjarnason, Ingvar [8 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Endoscop & Photodynam Med, Hamamatsu, Shizuoka 4313192, Japan
[2] Fujueda Municipal Gen Hosp, Dept Gastroenterol, Fujieda, Shizuoka, Japan
[3] Hamamatsu S Hosp, Gastroenterol Ctr, Hamamatsu, Shizuoka, Japan
[4] Hamamatsu Med Ctr, Dept Gastroenterol, Hamamatsu, Shizuoka, Japan
[5] Japan Immunores Labs, Takasaki, Gumma, Japan
[6] Seirei Gen Hosp, Dept Gastroenterol, Hamamatsu, Shizuoka, Japan
[7] Hamamatsu Univ Sch Med, Dept Med 1, Hamamatsu, Shizuoka 4313192, Japan
[8] GKT Med Sch, Dept Med, London, England
关键词
D O I
10.1053/jcgh.2003.50005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Active ulcerative colitis (UC) is characterized by infiltration of activated granulocytes and monocytes/macrophages (GM) within the large bowel mucosa. GM are major sources of inflammatory cytokines, and in UC they are elevated with increased survival time. We investigated the possibility that reducing the level of these cells might promote remission of active UC. Methods: Thirty-one patients with active corticosteroid refractory (refractory) UC, mean age of 42 years, duration of UC 6 years, clinical activity index (CAI) of 15, disease activity index (DAI) of 10, and 8 corticosteroid naive patients (naive), mean age of 36 years, duration of UC 2 years, CAI of 11, DAI of 8 were recruited. Each patient was treated with up to 11 cycles of granulocyte and monocyte adsorptive apheresis over 11 weeks by using a 335-mL capacity column filled with cellulose acetate beads that adsorb GM. Results: At week 12, 81% of refractory (CAI, 3; P < 0.001 and DAI, 4; P < 0.001) and 88% of naive (CAI, 1; P = 0.012 and DAI, 3; P = 0.011) patients achieved remission. Early relapse was not a feature, and at 12 months, 26 of 33 patients had maintained their remission. The treatment was well tolerated, and no severe side effects were observed. Conclusions: The outcome of this study suggests that reduction of circulating granulocytes and monocytes results in alleviation of inflammation and promotes clinical remission in patients with severe active UC that has not responded to intensive corticosteroid treatment. These data suggest that formal controlled studies are warranted.
引用
收藏
页码:28 / 35
页数:8
相关论文
共 45 条
[1]  
Allison MC, 1998, INFLAMMATORY BOWEL D
[2]   NONSTEROIDAL ANTIINFLAMMATORY DRUGS AND INFLAMMATORY BOWEL-DISEASE [J].
BJARNASON, I ;
MACPHERSON, A ;
SOMASLINDARAM, S ;
TEAHON, K .
CANADIAN JOURNAL OF GASTROENTEROLOGY, 1993, 7 (02) :160-169
[3]   INTESTINAL PERMEABILITY - AN OVERVIEW [J].
BJARNASON, I ;
MACPHERSON, A ;
HOLLANDER, D .
GASTROENTEROLOGY, 1995, 108 (05) :1566-1581
[4]  
BJARNASON I, 1994, INFLAMM BOWEL DIS, P53
[5]   Neutrophil apoptosis is delayed in patients with inflammatory bowel disease [J].
Brannigan, AE ;
O'Connell, PR ;
Hurley, H ;
O'Neill, A ;
Brady, HR ;
Fitzpatrick, JM ;
Watson, RWG .
SHOCK, 2000, 13 (05) :361-366
[6]   THE PRODUCTION OF CYTOKINES BY POLYMORPHONUCLEAR NEUTROPHILS [J].
CASSATELLA, MA .
IMMUNOLOGY TODAY, 1995, 16 (01) :21-26
[7]  
DARRIGO C, 1995, CLIN EXP IMMUNOL, V100, P173
[8]   Inflammatory bowel disease: Etiology and pathogenesis [J].
Fiocchi, C .
GASTROENTEROLOGY, 1998, 115 (01) :182-205
[9]   NEUTROPHILS, NITROGEN-OXIDES, AND INFLAMMATORY BOWEL-DISEASE [J].
GRISHAM, MB ;
YAMADA, T .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1992, 664 :103-115
[10]   Intravenous cyclosporin as rescue therapy in severe ulcerative colitis: time for a reappraisal? [J].
Hyde, GM ;
Thillainayagam, AV ;
Jewell, DP .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1998, 10 (05) :411-413