Therapeutic effect of an anti-Fas ligand mAb on lethal graft-versus-host disease

被引:55
作者
Miwa, K
Hashimoto, H
Yatomi, T
Nakamura, N
Nagata, S
Suda, T
机构
[1] Kanazawa Univ, Canc Res Inst, Ctr Dev Mol Target Drugs, Kanazawa, Ishikawa 9200934, Japan
[2] Osaka Univ, Sch Med, Dept Genet, Osaka 5650871, Japan
[3] Mochida Pharmaceut Co Ltd, Biosci Res Lab, Tokyo 1150043, Japan
[4] Osaka Univ, Sch Med, Dept Orthopaed Surg, Osaka 5650871, Japan
[5] Osaka Biosci Inst, Dept Biol Mol, Osaka 5650874, Japan
关键词
apoptosis; bone marrow transfer; cytotoxic T lymphocyte; disease model;
D O I
10.1093/intimm/11.6.925
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Several anti-fas ligand (FasL) inhibitory mAb (FLIM) were raised and characterized in this study. One, FLIM58, showed more potent neutralizing activity than Fas-Fc, the previously established artificial neutralizing agent for Fast. Several murine models of acute graft-versus-host disease (GVHD) after allogeneic bone marrow transplantation have been used to show that both Fast and perforin, the major effector molecules of cytotoxic T lymphocytes, are involved in this disease. In our GVHD model, Fast rather than perforin was associated with lethality. Administration of FLIM58 or Fas-Fc reduced the weight loss and mortality caused by GVHD, although other signs of GVHD, such as skin lesions, lymphoid hypoplasia and mononuclear cell infiltration in the liver did not improve significantly. FLIM58 was more effective than Fas-Fc in reducing mortality. Our results demonstrated that neutralizing agents for Fast are therapeutic for lethal GVHD.
引用
收藏
页码:925 / 931
页数:7
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