Publication:
Antibodies to a single, conserved epitope in anopheles APN1 inhibit universal transmission of plasmodium falciparum and plasmodium vivax malaria

dc.contributor.authorJennifer S. Armisteaden_US
dc.contributor.authorIsabelle Morlaisen_US
dc.contributor.authorDerrick K. Mathiasen_US
dc.contributor.authorJuliette G. Jardimen_US
dc.contributor.authorJaimy Joyen_US
dc.contributor.authorArthur Fridmanen_US
dc.contributor.authorAdam C. Finnefrocken_US
dc.contributor.authorAnsu Bagchien_US
dc.contributor.authorMagdalena Plebanskien_US
dc.contributor.authorDiana G. Scorpioen_US
dc.contributor.authorThomas S. Churcheren_US
dc.contributor.authorNatalie A. Borgen_US
dc.contributor.authorJetsumon Sattabongkoten_US
dc.contributor.authorRhoel R. Dinglasanaen_US
dc.contributor.otherJohns Hopkins Bloomberg School of Public Healthen_US
dc.contributor.otherInstitut de Recherche pour le Developpement Cameroonen_US
dc.contributor.otherMerck Research Laboratoriesen_US
dc.contributor.otherMonash Universityen_US
dc.contributor.otherThe Johns Hopkins School of Medicineen_US
dc.contributor.otherImperial College Londonen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherWalter and Eliza Hall Institute of Medical Researchen_US
dc.date.accessioned2018-11-09T02:22:43Z
dc.date.available2018-11-09T02:22:43Z
dc.date.issued2014-02-01en_US
dc.description.abstractMalaria transmission-blocking vaccines (TBVs) represent a promising approach for the elimination and eradication of this disease. AnAPN1 is a lead TBV candidate that targets a surface antigen on the midgut of the obligate vector of the Plasmodium parasite, the Anopheles mosquito. In this study, we demonstrated that antibodies targeting AnAPN1 block transmission of Plasmodium falciparum and Plasmodium vivax across distantly related anopheline species in countries to which malaria is endemic. Using a biochemical and immunological approach, we determined that the mechanism of action for this phenomenon stems from antibody recognition of a single protective epitope on AnAPN1, which we found to be immunogenic in murine and nonhuman primate models and highly conserved among anophelines. These data indicate that AnAPN1 meets the established target product profile for TBVs and suggest a potential key role for an AnAPN1-based panmalaria TBV in the effort to eradicate malaria.© 2014, American Society for Microbiology.en_US
dc.identifier.citationInfection and Immunity. Vol.82, No.2 (2014), 818-829en_US
dc.identifier.doi10.1128/IAI.01222-13en_US
dc.identifier.issn10985522en_US
dc.identifier.issn00199567en_US
dc.identifier.other2-s2.0-84893008833en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/33998
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84893008833&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleAntibodies to a single, conserved epitope in anopheles APN1 inhibit universal transmission of plasmodium falciparum and plasmodium vivax malariaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84893008833&origin=inwarden_US

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