Literature DB >> 7782255

The activity of halofuginone in immunosuppressed rats infected with Cryptosporidium parvum.

J E Rehg1.   

Abstract

Halofuginone was evaluated for its activity against experimentally induced infection due to Cryptosporidium parvum in rats rendered immunosuppressed with dexamethasone. The drug's activity was dose-related and both prophylaxis and therapy reduced the rate and severity of infection in the small intestine and caecum. Prophylactic treatment reduced infection of the common bile duct, but therapeutic administration did not and neither form of treatment reduced the infection rate in the colon. Intestinal infection recurred at a level comparable to that of untreated controls when treatment was discontinued. Treatment with halofuginone may reduce the severity of acute cryptosporidiosis, but is less efficacious for chronic cryptosporidiosis involving the colon and extraintestinal tissues, a manifestation increasingly seen in the immunocompromised host.

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Year:  1995        PMID: 7782255     DOI: 10.1093/jac/35.3.391

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  3 in total

1.  Transient neonatal Cryptosporidium parvum infection triggers long-term jejunal hypersensitivity to distension in immunocompetent rats.

Authors:  Rachel Marion; Asiya Baishanbo; Gilles Gargala; Arnaud François; Philippe Ducrotté; Celia Duclos; Jean Fioramonti; Jean Jacques Ballet; Loïc Favennec
Journal:  Infect Immun       Date:  2006-07       Impact factor: 3.441

2.  Validation of IMP dehydrogenase inhibitors in a mouse model of cryptosporidiosis.

Authors:  Suresh Kumar Gorla; Nina N McNair; Guangyi Yang; Song Gao; Ming Hu; Venkatakrishna R Jala; Bodduluri Haribabu; Boris Striepen; Gregory D Cuny; Jan R Mead; Lizbeth Hedstrom
Journal:  Antimicrob Agents Chemother       Date:  2013-12-23       Impact factor: 5.191

3.  Comparative evaluation of several techniques for purification of Cryptosporidium parvum oocysts from rat feces.

Authors:  P Suresh; J E Rehg
Journal:  J Clin Microbiol       Date:  1996-01       Impact factor: 5.948

  3 in total

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