Serum levels of soluble IL-2 receptor, IL-12, IL-18, and IFN-γ in patients with acute graft-versus-best disease after allogeneic bone marrow transplantation

被引:70
作者
Nakamura, H
Komatsu, K
Ayaki, M
Kawamoto, S
Murakami, M
Uoshima, N
Yagi, T
Hasegawa, T
Yasumi, M
Karasuno, T
Teshima, H
Hiraoka, A
Masaoka, T
机构
[1] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Tumor Biochem, Higashinari Ku, Osaka 5378511, Japan
[2] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Med 5, Higashinari Ku, Osaka 5378511, Japan
关键词
allogeneic bone marrow transplantation; acute graft-versus-host disease; soluble IL-2 receptor; IL-12; IL-18; IFN-gamma;
D O I
10.1067/mai.2000.106774
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Acute graft-versus-host disease still represents the major factor that limits successful allogeneic bone marrow transplantation. Cytokines released by type 1 T-helper cells are thought to play a pivotal role in acute graft-versus-host disease. Objective: This study was performed to investigate whether the serum levels of soluble IL-2 receptor, IL-12, IL-18, and IFN-gamma were associated with the manifestation of acute graft-versus-host disease. Methods: Serum cytokine levels were measured by sandwich ELISA in 18 patients who underwent allogeneic bone marrow transplantation. Results: Serum levels of soluble IL-2 receptor, IL-12, IL-18, and IFN-gamma were increased in patients in whom acute graft-versus-host disease developed. However, only serum soluble IL-2 receptor levels were significantly related to disease severity. Serum levels of IL-12 and IL-18, both of which are mainly produced by activated macrophages, were increased in different phases of acute graft-versus-host disease, especially grade I. Serum levels of soluble IL-2 receptor and IFN-gamma were significantly elevated in patients with fever. Conclusion: Serum levels of soluble IL-2 receptor were more closely related to the severity of acute graft-versus-host disease than those of IL-12, IL-18, and IFN-gamma.
引用
收藏
页码:S45 / S50
页数:6
相关论文
共 21 条
[1]  
ADAMS DH, 1989, LANCET, V1, P469
[2]  
Bonnotte B, 1996, EUR CYTOKINE NETW, V7, P389
[3]  
BUNJES D, 1995, BONE MARROW TRANSPL, V15, P727
[4]   THE MOLECULAR CELL BIOLOGY OF INTERFERON-GAMMA AND ITS RECEPTOR [J].
FARRAR, MA ;
SCHREIBER, RD .
ANNUAL REVIEW OF IMMUNOLOGY, 1993, 11 :571-611
[5]   The immunopathophysiology of acute graft-versus-host disease [J].
Ferrara, JLM ;
Cooke, KR ;
Pan, LY ;
Krenger, W .
STEM CELLS, 1996, 14 (05) :473-489
[6]  
Fujimori Y, 1998, BLOOD, V92, p332B
[7]  
FUKUDA H, 1994, BONE MARROW TRANSPL, V13, P181
[8]   LYMPHOKINE GENE-EXPRESSION INVIVO IS INHIBITED BY CYCLOSPORINE-A [J].
GRANELLIPIPERNO, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (02) :533-544
[9]  
Krenger W, 1996, J Hematother, V5, P3, DOI 10.1089/scd.1.1996.5.3
[10]   Cytokine cascades in acute graft-versus-host disease [J].
Krenger, W ;
Hill, GR ;
Ferrara, JLM .
TRANSPLANTATION, 1997, 64 (04) :553-558