Novel Synthetic Polyamines Are Effective in the Treatment of Experimental Microsporidiosis, an Opportunistic AIDS-Associated Infection

Author:

Bacchi Cyrus J.1,Weiss Louis M.23,Lane Schenella1,Frydman Benjamin4,Valasinas Aldonia4,Reddy Venodhar4,Sun Jerry S.4,Marton Laurence J.4,Khan Imitiaz A.5,Moretto Magali5,Yarlett Nigel1,Wittner Murray3

Affiliation:

1. Haskins Laboratories and Departments of Biology and Chemistry, Pace University, New York, New York

2. Departments of Medicine

3. Pathology Albert Einstein College of Medicine, Bronx, New York

4. SLIL Biomedical Corporation, Madison, Wisconsin

5. Department of Microbiology and Immunology, Louisiana State University Medical Center, New Orleans, Louisiana

Abstract

ABSTRACT Microsporidia are eukaryotic obligate intracellular protists that are emerging pathogens in immunocompromised hosts, such as patients with AIDS or patients who have undergone organ transplantation. We have demonstrated in vitro and in vivo that synthetic polyamine analogs are effective antimicrosporidial agents with a broad therapeutic window. CD8-knockout mice or nude mice infected with the microsporidian Encephalitozoon cuniculi were cured when they were treated with four different novel polyamine analogs at doses ranging from 1.25 to 5 mg/kg of body weight/day for a total of 10 days. Cured animals demonstrated no evidence of parasitemia by either PCR or histologic staining of tissues 30 days after untreated control animals died.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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