Journal of Gastroenterology

, Volume 33, Issue 1, pp 18–22 | Cite as

Cure of Helicobacter pylori infection by omeprazole-clarithromycin-based therapy in non-human primates

  • Andre Dubois
  • Douglas E. Berg
  • Nancy Fiala
  • Lillie M. Heman-Ackah
  • Guillermo I. Perez-Perez
  • Martin J. Blaser

Abstract:

Rhesus monkeys raised in colonies tend to become naturally infected by Helicobacter pylori early in life. Earlier attempts to cure H. pylori infection with a 10-day triple therapy (metronidazole, amoxicillin, and peptobismol) were only partially (60%) successful, probably because of preexisting metronidazole resistance. This study was carried out to determine the efficacy of an alternative clarithromycin-omeprazole-based therapy for curing H. pylori infection in Rhesus mon-keys (Macaca mulatta), and to examine histologic and serologic correlates of curing. Five monkeys were endoscoped under ketamine anesthesia. Histology and culture of gastric biopsies and serologic tests demonstrated that they were H. pylori-positive. Two animals had not received prior anti-H. pylori treatment, while three other animals had failed triple therapy and carried metronidazole-resistant H. pylori strains. Quadruple therapy with omeprazole, clarithromycin, amoxicillin, and bismuth subsalicylate was given for 10 days to these five animals. All five animals were cured of the infection, and remained H. pylori-free, based on histology and culture at regular intervals for the 5 months post-therapy during which they were followed. Gastritis scores and anti-H. pylori IgG levels decreased in each animal during this period to levels characteristic of uninfected animals. These results indicate that an omeprazole-clarithromycin-based regimen can cure H. pylori infection in Rhesus monkeys, with resolution of abnormal histology and serologic responses. They suggest that this preclinical animal model is useful for testing new anti-H. pylori therapies.

Key words:H. pylori treatment Rhesus monkeys gastritis immunoglobulins 

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Copyright information

© Springer-Verlag Tokyo 1998

Authors and Affiliations

  • Andre Dubois
    • 1
  • Douglas E. Berg
    • 3
  • Nancy Fiala
    • 1
  • Lillie M. Heman-Ackah
    • 2
  • Guillermo I. Perez-Perez
    • 4
  • Martin J. Blaser
    • 4
  1. 1.Laboratory of Gastrointestinal and Liver Studies, Digestive Diseases Division, Department of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814-4799, USAUS
  2. 2.Departments of Veterinary Medicine, Armed Forces Radiobiology Research Institute, Bethesda, MD, USAUS
  3. 3.Department of Molecular Microbiology, Washington University Medical School, St. Louis, MO, USAUS
  4. 4.Division of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine and Department of Veterans Affairs Medical Center, Nashville, TN, USAUS

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