Abstract
An immunosuppressed rat model was used to investigate the anti-Cryptosporidium parvum activity of sinefungin. In infected animals, oral sinefungin therapy resulted in a dose-related suppression of oocyst shedding, which correlated with oocyst disappearance from ileal sections. When administered prior to or on the day of oocyst challenge, sinefungin successfully prevented infection. These data suggest that sinefungin could be considered as a candidate molecule in the treatment of human cryptosporidiosis, considered to be the most significant enteric opportunistic infection in AIDS.
MeSH Terms
Adenosine/analogs & derivatives,therapeutic use
Animals
Antiprotozoal Agents/therapeutic use
Cryptosporidiosis/drug therapy,parasitology,prevention & control
Cryptosporidium parvum
Dose-Response Relationship, Drug
Feces/parasitology
Immunosuppression Therapy
Rats
Rats, Sprague-Dawley
Chemicals
Antiprotozoal Agents
Adenosine
sinefungin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Brasseur P
Department of Parasitology, Hôpital Charles Nicolle, Rouen, France.
Lemeteil D
Ballet J J
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