4.5 Article

Consistent Safety and Infectivity in Sporozoite Challenge Model of Plasmodium vivax in Malaria-Naive Human Volunteers

Journal

Publisher

AMER SOC TROP MED & HYGIENE
DOI: 10.4269/ajtmh.2011.09-0498

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Funding

  1. World Health Organization Initiative for Vaccine Research [LA35735G]
  2. National Institute of Allergy and Infectious Diseases (NIAID) [49486/TMRC]
  3. Colombian National Research Council
  4. COLCIENCIAS
  5. Ministry for Social Protection [253-2005, 207-2007]
  6. Malaria Vaccine and Drug Development Center Foundation

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A safe and reproducible Plasmodium vivax infectious challenge method is required to evaluate the efficacy of malaria vaccine candidates. Seventeen healthy Duffy (+) and five Duffy (-) subjects were randomly allocated into three (A-C) groups and were exposed to the bites of 2-4 Anopheles albimanus mosquitoes infected with Plasmodium vivax derived from three donors. Duffy (-) subjects were included as controls for each group. Clinical manifestations of malaria and parasitemia were monitored beginning 7 days post-challenge. All Duffy (+) volunteers developed patent malaria infection within 16 days after challenge. Prepatent period determined by thick smear, was longer for Group A (median 14.5 d) than for Groups B and C (median 10 d/each). Infected volunteers recovered rapidly after treatment with no serious adverse events. The bite of as low as two P vivax-infected mosquitoes provides safe and reliable infections in malaria-naive volunteers, suitable for assessing antimalarial and vaccine efficacy trials.

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