Potentiality of Interleukin-18 as a Useful Reagent for Treatment and Prevention of Leishmania major Infection

Author:

Ohkusu Kazunobu1,Yoshimoto Tomohiro123,Takeda Kiyoshi43,Ogura Takeharu1,Kashiwamura Shin-ichiro2,Iwakura Yoichiro5,Akira Shizuo43,Okamura Haruki23,Nakanishi Kenji123

Affiliation:

1. Department of Immunology and Medical Zoology1 and

2. Laboratory of Host Defenses, Institute for Advanced Medical Sciences,2 Hyogo College of Medicine, Nishinomiya, Hyogo 663-8501,

3. Core Research for Evolutional Science and Technology, Japan Science and Technology Corporation, Tokyo,3 Japan

4. Department of Host Defenses, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871,4

5. Laboratory Animal Research Center, Institute of Medical Science, University of Tokyo, Tokyo 108-8639,5 and

Abstract

ABSTRACT 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 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-γ) 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-γ. Our results also indicate the high potentiality of IL-18 as a useful reagent for treatment as well as prevention against reinfection.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference60 articles.

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2. Administration of monoclonal anti-IFNγ antibodies in vivo abrogates natural resistance of C3H/HeN mice to infection with Leishmania major;Belosevic M.;J. Immunol.,1989

3. Patterns of cytokine secretion in murine leishmaniasis: correlation with disease progression or resolution

4. Cloning of a novel receptor subunit, AcPL, required for interleukin-18 signaling;Born T. L.;J. Biol. Chem.,1998

5. Multiple Defects of Immune Cell Function in Mice with Disrupted Interferon-γ Genes

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