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Antimicrobial Agents and Chemotherapy, April 1999, p. 752-757, Vol. 43, No. 4
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Efficacy of RD3-0028 Aerosol Treatment against Respiratory Syncytial Virus Infection in Immunosuppressed Mice

Kenji Sudo,1,2,* Wataru Watanabe,1 Kenji Konno,1 Ryu Sato,3 Tsuyoshi Kajiyashiki,4 Shiro Shigeta,2 and Tomoyuki Yokota1

Rational Drug Design Laboratories, Fukushima 960-12421 and Department of Microbiology, Fukushima University School of Medicine,2 Fukushima 960-1295, Faculty of Engineering, Iwate University, Morioka, 020-8551,3 and Chemical Research Laboratory, Kuraray Co., Ltd., Kurashiki, 710-8691,4 Japan

Received 13 August 1998/Returned for modification 23 November 1998/Accepted 4 January 1999

RD3-0028, a benzodithiin compound, has antiviral activity against respiratory syncytial virus (RSV) in cell culture. We used a mouse model of RSV infection to determine the in vivo effect of RD3-0028. Cyclophosphamide (CYP)-treated, immunosuppressed mice were inoculated intranasally. The lungs of the mice were removed on day 4. The virus titers of the lungs of RD3-0028-treated mice were compared to the virus titers of the lungs of virus-inoculated, untreated control mice. In an effort to increase the therapeutic effectiveness of this compound, RD3-0028 was administered by aerosol to RSV-infected mice by using a head-exposure system. Aerosols generated from reservoirs containing RD3-0028 (7 mg/ml) administered for 2 h twice daily for 3 days significantly reduced the pulmonary titer of RSV-infected mice. It is clear that the minimal effective dose of RD3-0028 for RSV-infected mice is significantly less than that of ribavirin, the only compound currently available for use against RSV disease. Furthermore, the RD3-0028 aerosol administration appeared to protect the lungs of infected, CYP-treated mice against tissue damage, as evidenced by the preservation of the lung architecture and a reduction in pulmonary inflammatory infiltrates. RD3-0028 aerosol was not toxic for mice at the therapeutic dose. The present study demonstrates the effectiveness of aerosol administration of RD3-0028 for RSV-infected mice.


* Corresponding author. Mailing address: Fukushima University School of Medicine, Hikarigaoka 1, Fukushima 960-1295, Japan. Phone: 81-24-548-2111. Fax: 81-24-548-5072.


Antimicrobial Agents and Chemotherapy, April 1999, p. 752-757, Vol. 43, No. 4
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



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Copyright © 1999 by the American Society for Microbiology. All rights reserved.