Potentiality of interleukin-18 as a useful reagent for treatment and prevention of Leishmania major infection

被引:84
作者
Ohkusu, K
Yoshimoto, T
Takeda, K
Ogura, T
Kashiwamura, S
Iwakura, Y
Akira, S
Okamura, H
Nakanishi, K
机构
[1] Hyogo Coll Med, Dept Immunol & Med Zool, Nishinomiya, Hyogo 6638501, Japan
[2] Hyogo Coll Med, Host Def Lab, Inst Adv Med Sci, Nishinomiya, Hyogo 6638501, Japan
[3] Osaka Univ, Microbial Dis Res Inst, Dept Host Def, Osaka 5650871, Japan
[4] Univ Tokyo, Inst Med Sci, Lab Anim Res Ctr, Tokyo 1088639, Japan
[5] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Tokyo, Japan
关键词
D O I
10.1128/IAI.68.5.2449-2456.2000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-18 (IL-18) is a proinflammatory cytokine that plays an important role in natural killer cell activation and the T helper 1 (Th1) cell response, particularly in collaboration with IL-12. Since Th1 cells play a pivotal role in the host defense against infection with intracellular microbes, such as Leishmania major, we investigated whether IL-18 is critically involved in protection against L. major infection by activation of Th1 cells. We administered IL-12 and/or IL-18 daily to L. major-susceptible BALB/c mice. Neither IL-12 (10 ng/ mouse) nor IL-18 (1,000 ng/mouse) induced wound healing, while daily injection of IL-12 and IL-18 during the first week after infection strongly protected the mice from footpad swelling by induction and activation of Th1 cells. Furthermore, these mice acquired protective immunity. We also in investigated a protective role of endogenous IL-18 by using anti-IL-18 antibody-treated C3H/HeN mice (an L. major-resistant strain) or IL-18 deficient (IL-18(-/-)) mice with a resistant background (C57BL/6). We found that in the absence of endogenous IL-18, these mice showed prolonged footpad swelling as well as diminished nitric oxide production. However, daily injection of IL-18 into IL-18(-/-) mice corrected their deficiencies, suggesting that these mice have Th1 cells that produce gamma interferon (IFN-gamma) in response to IL-18. Indeed, these mice had normal levels of Th1 cells. Thus, IL-18 is not responsible for inducing Th1 cells but participates in host resistance by its action in stimulating Th1 cells to produce IFN-gamma. Our results also indicate the high potentiality of IL-18 as a useful reagent for treatment as well as prevention against reinfection.
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收藏
页码:2449 / 2456
页数:8
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