Leukocyte adsorptive apheresis for the treatment of active ulcerative colitis: A prospective, uncontrolled, pilot study

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...

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Veröffentlicht in:Clinical gastroenterology and hepatology 2003, Vol.1 (1), p.28-35
Hauptverfasser: Hanai, Hiroyuki, Watanabe, Fumitoshi, Takeuchi, Ken, Iida, Takayuki, Yamada, Masami, Iwaoka, Yasushi, Saniabadi, Abby, Matsushita, Isao, Sato, Yoshihiko, Tozawa, Kotaro, Arai, Hajime, Furuta, Takahisa, Sugimoto, Ken, Bjarnason, Ingvar
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container_end_page 35
container_issue 1
container_start_page 28
container_title Clinical gastroenterology and hepatology
container_volume 1
creator Hanai, Hiroyuki
Watanabe, Fumitoshi
Takeuchi, Ken
Iida, Takayuki
Yamada, Masami
Iwaoka, Yasushi
Saniabadi, Abby
Matsushita, Isao
Sato, Yoshihiko
Tozawa, Kotaro
Arai, Hajime
Furuta, Takahisa
Sugimoto, Ken
Bjarnason, Ingvar
description 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. CLINICAL GASTROENTEROLOGY AND HEPATOLOGY 2003;1:28-35
doi_str_mv 10.1053/jcgh.2003.50005
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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 &lt; 0.001 and DAI, 4; P &lt; 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. 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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 &lt; 0.001 and DAI, 4; P &lt; 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. 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Watanabe, Fumitoshi ; Takeuchi, Ken ; Iida, Takayuki ; Yamada, Masami ; Iwaoka, Yasushi ; Saniabadi, Abby ; Matsushita, Isao ; Sato, Yoshihiko ; Tozawa, Kotaro ; Arai, Hajime ; Furuta, Takahisa ; Sugimoto, Ken ; Bjarnason, Ingvar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-33866bdb994c462f478d3c93bd8f3fd020ce6b87a849becaa0cbe330c01d07b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Colitis, Ulcerative - therapy</topic><topic>Colonoscopy</topic><topic>Female</topic><topic>Granulocytes</topic><topic>Humans</topic><topic>Leukapheresis</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Monocytes</topic><topic>Pilot Projects</topic><topic>Prospective Studies</topic><topic>Remission Induction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hanai, Hiroyuki</creatorcontrib><creatorcontrib>Watanabe, Fumitoshi</creatorcontrib><creatorcontrib>Takeuchi, Ken</creatorcontrib><creatorcontrib>Iida, Takayuki</creatorcontrib><creatorcontrib>Yamada, Masami</creatorcontrib><creatorcontrib>Iwaoka, Yasushi</creatorcontrib><creatorcontrib>Saniabadi, Abby</creatorcontrib><creatorcontrib>Matsushita, Isao</creatorcontrib><creatorcontrib>Sato, Yoshihiko</creatorcontrib><creatorcontrib>Tozawa, Kotaro</creatorcontrib><creatorcontrib>Arai, Hajime</creatorcontrib><creatorcontrib>Furuta, Takahisa</creatorcontrib><creatorcontrib>Sugimoto, Ken</creatorcontrib><creatorcontrib>Bjarnason, Ingvar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hanai, Hiroyuki</au><au>Watanabe, Fumitoshi</au><au>Takeuchi, Ken</au><au>Iida, Takayuki</au><au>Yamada, Masami</au><au>Iwaoka, Yasushi</au><au>Saniabadi, Abby</au><au>Matsushita, Isao</au><au>Sato, Yoshihiko</au><au>Tozawa, Kotaro</au><au>Arai, Hajime</au><au>Furuta, Takahisa</au><au>Sugimoto, Ken</au><au>Bjarnason, Ingvar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leukocyte adsorptive apheresis for the treatment of active ulcerative colitis: A prospective, uncontrolled, pilot study</atitle><jtitle>Clinical gastroenterology and hepatology</jtitle><addtitle>Clin Gastroenterol Hepatol</addtitle><date>2003</date><risdate>2003</risdate><volume>1</volume><issue>1</issue><spage>28</spage><epage>35</epage><pages>28-35</pages><issn>1542-3565</issn><eissn>1542-7714</eissn><abstract>Background &amp; 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 &lt; 0.001 and DAI, 4; P &lt; 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. CLINICAL GASTROENTEROLOGY AND HEPATOLOGY 2003;1:28-35</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15017514</pmid><doi>10.1053/jcgh.2003.50005</doi><tpages>8</tpages></addata></record>
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subjects Adult
Aged
Colitis, Ulcerative - therapy
Colonoscopy
Female
Granulocytes
Humans
Leukapheresis
Leukocyte Count
Male
Middle Aged
Monocytes
Pilot Projects
Prospective Studies
Remission Induction
title Leukocyte adsorptive apheresis for the treatment of active ulcerative colitis: A prospective, uncontrolled, pilot study
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