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Antimicrobial Agents and Chemotherapy, October 1998, p. 2542-2548, Vol. 42, No. 10
Division of Infectious Diseases,
Received 5 February 1998/Returned for modification 24 March
1998/Accepted 15 July 1998
Current therapy for leishmaniasis is unsatisfactory because
parenteral antimonial salts and pentamidine are associated with significant toxicity and failure rates. We examined the efficacy of
KY62, a new, water-soluble, polyene antifungal, against cutaneous infection with Leishmania amazonensis and against visceral
infection with Leishmania donovani in susceptible BALB/c
mice. Mice were infected with L. amazonensis promastigotes
in the ear pinna and in the tail and were treated with KY62 or
amphotericin B. The cutaneous lesions showed a remarkable response to
therapy with KY62 at a dose of 30 mg per kg of body weight per day. At
this dose, the efficacy of KY62 was equivalent to or better than that of amphotericin B at 1 to 5 mg/kg/day. Mice infected intravenously with
107 L. donovani promastigotes and treated with
KY62 showed a 4-log reduction in the parasite burden in the liver and
spleen compared to untreated mice. These studies indicate potent
activity of KY62 against experimental cutaneous leishmaniasis caused by
L. amazoniensis and against experimental visceral
leishmaniasis caused by L. donovani.
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Efficacies of KY62 against Leishmania amazonensis and
Leishmania donovani in Experimental Murine Cutaneous
Leishmaniasis and Visceral Leishmaniasis
*
Corresponding author. Mailing address: Division of
Infectious Diseases, Department of Medicine, The University of Texas
Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78284. Phone: (210) 567-4823. Fax: (210) 567-4670. E-mail: abdely{at}uthscsa.edu.
Antimicrobial Agents and Chemotherapy, October 1998, p. 2542-2548, Vol. 42, No. 10
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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