Systemic administration of interferon-γ-expressing plasmid reduces late allergic bronchitis in a mouse model of asthma

被引:8
作者
Hayashi, T [1 ]
Maeda, K
Hasegawa, K
Nakai, S
Hamachi, T
Iwata, H
机构
[1] Yamaguchi Univ, Fac Agr, Lab Vet Pathol, Yamaguchi 7538515, Japan
[2] Yamaguchi Univ, Fac Agr, Lab Vet Microbiol, Yamaguchi 753, Japan
[3] Yamaguchi Univ, Fac Agr, Lab Vet Hyg, Yamaguchi 753, Japan
关键词
plasmid; IFN-gamma; asthma; mouse; model; Th2;
D O I
10.1046/j.1365-2613.2002.00218.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Asthma might be caused by a helper T(Th)2 immune response. We hypothesized that the systemic administration of the Th1 cytokines may reduce the Th2 type late asthmatic response (LAR). We examined the effect of the intraperitoneal injection of interferon(IFN)-gamma-expressing plasmid, a Th1 cytokine, or interleukin(IL)-4-expressing plasmid, a Th2 cytokine, at the time of sensitization on a mouse model of asthma induced by ovalbumin in BALB/c mice. We demonstrated that the IFN-gamma-expressing plasmid reduced the LAR, whereas the IL-4-expressing plasmid enhanced the LAR as compared with the saline or plasmid-only treated group. The present study suggests that the systemic administration of IFN-gamma-expressing plasmid may have a modulating ability of Th1/Th2 balance to down-regulate Th2 response by a mutual inhibitory mechanism between Th1 and Th2 cells, leading to the reduction of the LAR.
引用
收藏
页码:81 / 86
页数:6
相关论文
共 20 条
[1]   INTERLEUKIN-2, INTERLEUKIN-4 AND INTERLEUKIN-5 ARE SEQUENTIALLY PRODUCED IN MITOGEN-STIMULATED MURINE SPLEEN-CELL CULTURES [J].
CARDELL, S ;
SANDER, B .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (02) :389-395
[2]   IL-4 promotes airway eosinophilia by suppressing IFN-γ production:: Defining a novel role for IFN-γ in the regulation of allergic airway inflammation [J].
Cohn, L ;
Herrick, C ;
Niu, NQ ;
Homer, RJ ;
Bottomly, K .
JOURNAL OF IMMUNOLOGY, 2001, 166 (04) :2760-2767
[3]   PERIPHERAL-BLOOD CD4 BUT NOT CD8 T-LYMPHOCYTES IN PATIENTS WITH EXACERBATION OF ASTHMA TRANSCRIBE AND TRANSLATE MESSENGER-RNA ENCODING CYTOKINES WHICH PROLONG EOSINOPHIL SURVIVAL IN THE CONTEXT OF A TH2-TYPE PATTERN - EFFECT OF GLUCOCORTICOID THERAPY [J].
CORRIGAN, CJ ;
HAMID, Q ;
NORTH, J ;
BARKANS, J ;
MOQBEL, R ;
DURHAM, S ;
GEMOUENGESAETH, V ;
KAY, AB .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 12 (05) :567-578
[4]   Interleukin 4, but not interleukin 5 or eosinophils, is required in a murine model of acute airway hyperreactivity [J].
Corry, DB ;
Folkesson, HG ;
Warnock, ML ;
Erle, DJ ;
Matthay, MA ;
WienerKronish, JP ;
Locksley, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) :109-117
[5]   Systemic and local interferon γ gene delivery to the lungs for treatment of allergen-induced airway hyperresponsiveness in mice [J].
Dow, SW ;
Schwarze, J ;
Heath, TD ;
Potter, TA ;
Gelfand, EW .
HUMAN GENE THERAPY, 1999, 10 (12) :1905-1914
[6]   Complexity and redundancy in the pathogenesis of asthma: Reassessing the roles of mast cells and T cells [J].
Galli, SJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (03) :343-347
[7]   CLONING AND EXPRESSION OF MURINE IMMUNE INTERFERON CDNA [J].
GRAY, PW ;
GOEDDEL, DV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (19) :5842-5846
[8]   CD80 costimulation is essential for the induction of airway eosinophilia [J].
Harris, N ;
Peach, R ;
Naemura, J ;
Linsley, PS ;
LeGros, G ;
Ronchese, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) :177-182
[9]   Bronchial lesions of the late asthmatic response in BALB/c and C57BL/6 mice [J].
Hayashi, T ;
Hasegawa, K ;
Nakai, S ;
Hamachi, T ;
Adachi, Y ;
Yamauchi, Y ;
Maeda, K .
JOURNAL OF COMPARATIVE PATHOLOGY, 2001, 125 (2-3) :208-213
[10]  
Kline JN, 1998, J IMMUNOL, V160, P2555