Increased soluble Fas-ligand in sera of bone marrow transplant recipients with acute graft-versus-host disease

被引:53
作者
Kanda, Y
Tanaka, Y
Shirakawa, K
Yatomi, T
Nakamura, N
Kami, M
Saito, T
Izutsu, K
Asai, T
Yuji, K
Ogawa, S
Honda, H
Mitani, K
Chiba, S
Yazaki, Y
Hirai, H
机构
[1] Univ Tokyo, Fac Med, Dept Cell Therapy & Transplantat Med, Bunkyo Ku, Tokyo 113, Japan
[2] Univ Tokyo, Fac Med, Dept Internal Med 3, Tokyo 113, Japan
[3] Mochida Pharmaceut Co, Biosci Res Lab, Tokyo, Japan
关键词
bone marrow transplantation; graft-versus-host disease; Fas; soluble Fas ligand;
D O I
10.1038/sj.bmt.1701427
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Acute graft-versus-host disease (aGVHD) is a major complication following allogeneic bone marrow transplantation (BMT). Recently, accumulating evidence indicates that the Fas/Fas ligand (FasL) system is implicated in the pathogenesis of aGVHD in murine models, We determined the serum levels of soluble Fast (sFasL) in BMT recipients using an enzyme-linked immunosorbent assay. The serum sFasL was suppressed during the period of myelosuppression following the preparative regimen and subsequently increased with hematopoietic reconstitution after BMT, In patients with aGVHD, the serum sFasL level was significantly higher than in those without aGVHD, In the mixed lymphocyte reaction assay, sFasL in the supernatants was increased with a significant correlation to the level of H-3-thymidine uptake. Our findings suggest that the Fas/FasL system is activated by allogeneic stimulation and may have close correlation to the development of aGVHD in human BMT.
引用
收藏
页码:751 / 754
页数:4
相关论文
共 19 条
[1]   T-CELL RECEPTOR-INDUCED FAS LIGAND EXPRESSION IN CYTOTOXIC T-LYMPHOCYTE CLONES IS BLOCKED BY PROTEIN-TYROSINE KINASE INHIBITORS AND CYCLOSPORINE-A [J].
ANEL, A ;
BUFERNE, M ;
BOYER, C ;
SCHMITTVERHULST, AM ;
GOLSTEIN, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (10) :2469-2476
[2]   The role of cell-mediated cytotoxicity in acute GVHD after MHC-matched allogeneic bone marrow transplantation in mice [J].
Baker, MB ;
Altman, NH ;
Podack, ER ;
Levy, RB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (06) :2645-2656
[3]   Cytotoxic T cells deficient in both functional fas ligand and perforin show residual cytolytic activity yet lose their capacity to induce lethal acute graft-versus-host disease [J].
Braun, MY ;
Lowin, B ;
French, L ;
AchaOrbea, H ;
Tschopp, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (02) :657-661
[4]   A metalloproteinase inhibitor prevents lethal acute graft-versus-host disease in mice [J].
Hattori, K ;
Hirano, T ;
Ushiyama, C ;
Miyajima, H ;
Yamakawa, N ;
Ebata, T ;
Wada, Y ;
Ikeda, S ;
Yoshino, K ;
Tateno, M ;
Oshimi, K ;
Kayagaki, N ;
Yagita, H ;
Okumura, K .
BLOOD, 1997, 90 (02) :542-548
[5]   Differential effects of anti-Fas ligand and anti-tumor necrosis factor α antibodies on acute graft-versus-host disease pathologies [J].
Hattori, K ;
Hirano, T ;
Miyajima, H ;
Yamakawa, N ;
Tateno, M ;
Oshimi, K ;
Kayagaki, N ;
Yagita, H ;
Okumura, K .
BLOOD, 1998, 91 (11) :4051-4055
[6]  
HERVE P, 1990, BLOOD, V75, P1017
[7]  
HERVE P, 1992, BLOOD, V79, P3362
[8]   METALLOPROTEINASE-MEDIATED RELEASE OF HUMAN FAS LIGAND [J].
KAYAGAKI, N ;
KAWASAKI, A ;
EBATA, T ;
OHMOTO, H ;
IKEDA, S ;
INOUE, S ;
YOSHINO, K ;
OKUMURA, K ;
YAGITA, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) :1777-1783
[9]  
KORNGOLD R, 1978, J EXP MED, V148, P1687
[10]   Difference in the expression of Fas/Fas-ligand and the lymphocyte subset reconstitution according to the occurrence of acute GVHD [J].
Lee, S ;
Chong, SY ;
Lee, JW ;
Kim, SC ;
Min, YH ;
Hahn, JS ;
Ko, YW .
BONE MARROW TRANSPLANTATION, 1997, 20 (10) :883-888