Interleukin 18 (IL-18) in synergy with IL-2 induces lethal lung injury in mice: A potential role for cytokines, chemokines, and natural killer cells in the pathogenesis of interstitial pneumonia

被引:83
作者
Okamoto, M
Kato, S
Oizumi, K
Kinoshita, M
Inoue, Y
Hoshino, K
Akira, S
Mckenzie, ANJ
Young, HA
Hoshino, T
机构
[1] Kurume Univ, Sch Med, Dept Internal Med 1, Kurume, Fukuoka 8300011, Japan
[2] Kurume Univ, Sch Med, Dept Pathol, Kurume, Fukuoka 8300011, Japan
[3] Nippon Organon, Div Res & Dev, R&D Labs, Osaka, Japan
[4] Osaka Univ, Res Inst Microbial Dis, Dept Host Def, Suita, Osaka 565, Japan
[5] Japan Sci & Technol Corp, CREST, Suita, Osaka, Japan
[6] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[7] NCI, Expt Immunol Lab, Frederick, MD 21701 USA
关键词
D O I
10.1182/blood.V99.4.1289
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Interleukin 18 (IL-18) was discovered as an interferon-gamma (IFN-gamma)-inducing factor and plays important roles in natural killer (NK) cell activation. IL-18 also induces proinflammatory cytokines; chemokines; helper T-cell 2 (T(H)2) cytokines (eg, IL-4, IL-13); and immunoglobulin E (Ig-E) and IgG1 production. The combination of IL-18 plus IL-2 or IL-12 up-regulates IFN-gamma gene expression and NK cytotoxicity and has synergistic antitumor activity in vivo and in vitro. Here it is reported that daily administration of IL-18 with IL-2, but not of IL-18 or IL-2 alone, induces lethal lung injury in normal mice, but not in IL-18 receptor alpha (IL-1 receptor-related protein)-deficient (IL-18 receptor alpha(-/-)) mice. Marked interstitial infiltration of lymphocytes, composed mainly of NK cells, was found in the lungs of IL-18/IL-2-treated mice. Increased cytokine and chemokine levels were observed in the sera and lungs of IL-18/IL-2-treated mice. Administration of IL-18/IL-2 was also lethal to mice treated with a metalloproteinase inhibitor, which inhibited tumor necrosis factor-alpha and Fas-ligand release. While IFN-gamma(-/-) mice were partially resistant to the treatment, IL-4(-/-), IL-13(-/-), IL-4/IL-13(-/-), and Stat6(-/-) mice were sensitive, to IL-18/IL-2, indicating that these genes were not involved in the host response. The lethal effect by IL-18/IL-2 was completely eliminated in severe combined immunodeficient mice pretreated with antiasialo-GM1 antibody and normal mice pretreated with anti-NK1.1 but not with anti-CD4 or anti-CD8, monoclonal antibody. These results suggest that specific cytokines, chemokines, and NK cells are involved in the pathogenesis of interstitial pneumonia. These results suggest that the clinical use of this interleukin may result in unexpected physiological consequences. (C) 2002 by The American Society of Hematology.
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页码:1289 / 1298
页数:10
相关论文
共 50 条
[1]   The role of IL-18 in innate immunity [J].
Akira, S .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (01) :59-63
[2]  
ANDERSON TD, 1988, LAB INVEST, V59, P598
[3]   Acute interstitial pneumonia [J].
Bouros, D ;
Nicholson, AC ;
Polychronopoulos, V ;
du Bois, RM .
EUROPEAN RESPIRATORY JOURNAL, 2000, 15 (02) :412-418
[4]   Coadministration of interleukin-18 and interleukin-12 induces a fatal inflammatory response in mice:: critical role of natural killer cell interferon-γ production and STAT-mediated signal transduction [J].
Carson, WE ;
Dierksheide, JE ;
Jabbour, S ;
Angheina, M ;
Bouchard, P ;
Ku, G ;
Yu, HX ;
Baumann, H ;
Shah, MH ;
Cooper, MA ;
Durbin, J ;
Caligiuri, MA .
BLOOD, 2000, 96 (04) :1465-1473
[5]  
Carson WE, 1999, J IMMUNOL, V162, P4943
[6]   THE EFFECT OF DEFEROXAMINE ON BLEOMYCIN-INDUCED LUNG FIBROSIS IN THE HAMSTER [J].
CHANDLER, DB ;
FULMER, JD .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1985, 131 (04) :596-598
[7]   Attenuation of lung inflammation and fibrosis in interferon-γ-deficient mice after intratracheal bleomycin [J].
Chen, ES ;
Greenlee, BM ;
Wills-Karp, M ;
Moller, DR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 24 (05) :545-555
[8]   IL-18:: A TH1-inducing, proinflammatory cytokine and new member of the IL-1 family [J].
Dinarello, CA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 103 (01) :11-24
[9]  
Fogler WE, 1996, J IMMUNOL, V156, P4707
[10]   PASSIVE-IMMUNIZATION AGAINST TUMOR NECROSIS FACTOR PARTIALLY ABROGATES INTERLEUKIN-2 TOXICITY [J].
FRAKER, DL ;
LANGSTEIN, HN ;
NORTON, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (03) :1015-1020