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Immunisation against a serine protease inhibitor reduces intensity of Plasmodium berghei infection in mosquitoes
Authors:Andrew R Williams  Sara E Zakutansky  Kazutoyo Miura  Matthew DJ Dicks  Thomas S Churcher  Kerry E Jewell  Aisling M Vaughan  Alison V Turner  Melissa C Kapulu  Kristin Michel  Carole A Long  Robert E Sinden  Adrian VS Hill  Simon J Draper  Sumi Biswas
Institution:1. The Jenner Institute, University of Oxford, Roosevelt Drive, Oxford OX3 7DQ, UK;2. Laboratory of Malaria and Vector Research, NIAID, NIH, Rockville, MD 20852, USA;3. Department of Infectious Disease Epidemiology, Imperial College London, London, UK;4. Kansas State University, Division of Biology, Manhattan, KS 66506, USA;5. Division of Cell and Molecular Biology, Imperial College London, London, UK
Abstract:The mosquito innate immune response is able to clear the majority of Plasmodium parasites. This immune clearance is controlled by a number of regulatory molecules including serine protease inhibitors (serpins). To determine whether such molecules could represent a novel target for a malaria transmission-blocking vaccine, we vaccinated mice with Anopheles gambiae serpin-2. Antibodies against Anopheles gambiae serpin-2 significantly reduced the infection of a heterologous Anopheles species (Anopheles stephensi) by Plasmodium berghei, however this effect was not observed with Plasmodium falciparum. Therefore, this approach of targeting regulatory molecules of the mosquito immune system may represent a novel approach to transmission-blocking malaria vaccines.
Keywords:Malaria  Vaccine  Mosquito  Antibodies  Serpins
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