Induction of heme oxygenase-1 before conditioning results in improved survival and reduced graft-versus-host disease after experimental allogeneic bone marrow transplantation

被引:33
作者
Gerbitz, A
Ewing, P
Wilke, A
Schubert, T
Eissner, G
Dietl, B
Andreesen, R
Cooke, KR
Holler, E
机构
[1] Univ Munich, Dept Hematol Oncol, D-81377 Munich, Germany
[2] Univ Regensburg, Dept Hematol Oncol, D-8400 Regensburg, Germany
[3] Univ Regensburg, Dept Pathol, D-8400 Regensburg, Germany
[4] Univ Regensburg, Dept Radiat Therapy, D-8400 Regensburg, Germany
[5] Univ Michigan, Ctr Canc, Dept Pediat,Div Hematol & Oncol, Blood & Marrow Stem Cell Transplantat Program, Ann Arbor, MI 48109 USA
关键词
GVHD e; cytokines; heme oxygenase; BMT; LPS; protoporphyrin; CoPP;
D O I
10.1016/j.bbmt.2004.04.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acute graft-versus-host disease (aGVHD) remains one of the main obstacles after allogeneic bone marrow transplantation (BMT). Using a well-established mouse BMT model in which aGVHD is induced across a haploidentical mismatch, we show that the expression of heme oxygenase-1 (HO-1) can be induced by cobalt-protoporphyrin IX (CoPP) in aGVHD target organs such as liver and bowel and that the induction of HO-1 before BMT results in improved overall survival and reduced aGVHD. Serum levels of proinflammatory cytokines were markedly reduced in CoPP-treated animals. Recipients displayed less damage to the intestinal mucosa, and this resulted in reduced serum lipopolysaccharide levels at day 6 after transplantation. Peritoneal cells and CD45(+) liver cells isolated from mice that received transplants strongly expressed HO-1 and displayed a reduction in the expression of activation markers such as CD11b, CD80, and major histocompatibility complex class I. This resulted in reduced T-cell activation ex vivo. These results demonstrate that the induction of HO-1 before high-dose conditioning protects the host in multiple ways and effectively ameliorates aGVHD. (C) 2004 American Society for Blood and Marrow Transplantationy.
引用
收藏
页码:461 / 472
页数:12
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