Elevated interleukin (IL)-18 levels during acute graft-versus-host disease after allogeneic bone marrow transplantation

被引:70
作者
Fujimori, Y
Takatsuka, H
Takemoto, Y
Hara, H
Okamura, H
Nakanishi, K
Kakishita, E
机构
[1] Hyogo Coll Med, Dept Internal Med 2, Nishinomiya, Hyogo 6638501, Japan
[2] Hyogo Coll Med, Dept Transfus Med, Nishinomiya, Hyogo 6638501, Japan
[3] Hyogo Coll Med, Inst Adv Med Sci, Host Def Lab, Nishinomiya, Hyogo 6638501, Japan
[4] Hyogo Coll Med, Dept Immunol & Med Zool, Nishinomiya, Hyogo 6638501, Japan
关键词
interleukin; 18; bone marrow transplantation; graft-versus-host disease; type 1 T cells; interferon gamma;
D O I
10.1046/j.1365-2141.2000.02095.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acute graft-versus-host disease (aGVHD) after allogeneic bone marrow transplantation (BMT) is mediated by grafted T lymphocytes after their polarization into type 1 T cells. Interleukin (IL)-18, a novel immunoregulatory cytokine, strongly stimulates type 1 T cells, therefore we postulated that IL-18 may be involved in the pathogenesis of aGVHD. Using an enzyme-linked immunosorbent assay (ELISA), we serially measured serum levels of IL-18 in 37 patients with haematological malignancy before and after allogeneic BMT. Patients with aGVHD had high levels of IL-18 that strongly correlated with the severity of aGVHD. We also found that they showed reduced serum levels of IL-18 after appropriate treatment or at a state of resolution. IL-18 levels were not affected by the pretransplant regimen, engraftment or bacterial infection. Compared with circulating interferon (IFN)-gamma or IL-12 levels, serum levels of IL-18 showed a more sensitive and specific correlation with the disease status of aGVHD, These findings suggest that IL-18 may play important roles in the pathogenesis of aGVHD and that measurement of serum IL-18 levels can be useful indicator of aGVHD.
引用
收藏
页码:652 / 657
页数:6
相关论文
共 30 条
[1]  
Bonnotte B, 1996, EUR CYTOKINE NETW, V7, P389
[2]   CYCLOSPORINE, METHOTREXATE, AND PREDNISONE COMPARED WITH CYCLOSPORINE AND PREDNISONE FOR PROPHYLAXIS OF ACUTE GRAFT-VERSUS-HOST DISEASE [J].
CHAO, NJ ;
SCHMIDT, GM ;
NILAND, JC ;
AMYLON, MD ;
DAGIS, AC ;
LONG, GD ;
NADEMANEE, AP ;
NEGRIN, RS ;
ODONNELL, MR ;
PARKER, PM ;
SMITH, EP ;
SNYDER, DS ;
STEIN, AS ;
WONG, RM ;
BLUME, KG ;
FORMAN, SJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (17) :1225-1230
[3]   Interferon-gamma-inducing factor, a novel cytokine, enhances Fas ligand-mediated cytotoxicity of murine T helper 1 cells [J].
Dao, T ;
Ohashi, K ;
Kayano, T ;
Kurimoto, M ;
Okamura, H .
CELLULAR IMMUNOLOGY, 1996, 173 (02) :230-235
[4]   Overview of interleukin-18:: more than an interferon-γ inducing factor [J].
Dinarello, CA ;
Novick, D ;
Puren, AJ ;
Fantuzzi, G ;
Shapiro, L ;
Mühl, H ;
Yoon, DY ;
Reznikov, LL ;
Kim, SH ;
Rubinstein, M .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 63 (06) :658-664
[5]   Biologic basis for interleukin-1 in disease [J].
Dinarello, CA .
BLOOD, 1996, 87 (06) :2095-2147
[6]   Interleukin-18 regulation of interferon γ production and cell proliferation as shown in interleukin-1β-converting enzyme (Caspase-1)-deficient mice [J].
Fantuzzi, G ;
Puren, AJ ;
Harding, MW ;
Livingston, DJ ;
Dinarello, CA .
BLOOD, 1998, 91 (06) :2118-2125
[7]   THE MOLECULAR CELL BIOLOGY OF INTERFERON-GAMMA AND ITS RECEPTOR [J].
FARRAR, MA ;
SCHREIBER, RD .
ANNUAL REVIEW OF IMMUNOLOGY, 1993, 11 :571-611
[8]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[9]   Activation of interferon-gamma inducing factor mediated by interleukin-1 beta converting enzyme [J].
Gu, Y ;
Kuida, K ;
Tsutsui, H ;
Ku, G ;
Hsiao, K ;
Fleming, MA ;
Hayashi, N ;
Higashino, K ;
Okamura, H ;
Nakanishi, K ;
Kurimoto, M ;
Tanimoto, T ;
Flavell, RA ;
Sato, V ;
Harding, MW ;
Livingston, DJ ;
Su, MSS .
SCIENCE, 1997, 275 (5297) :206-209
[10]  
Kichian K, 1996, J IMMUNOL, V157, P2851