Identification of an Immunogenic Broadly Inhibitory Surface Epitope of the Plasmodium vivax Duffy Binding Protein Ligand Domain

Author:

George Miriam T.1,Schloegel Jesse L.1,Ntumngia Francis B.1ORCID,Barnes Samantha J.1,King Christopher L.2,Casey Joanne L.3,Foley Michael3,Adams John H.1ORCID

Affiliation:

1. Center for Global Health and Infectious Disease Research, Department of Global Health, University of South Florida, Tampa, Florida, USA

2. Center for Global Health and Diseases, Case Western Reserve University, Cleveland, Ohio, USA

3. Department of Biochemistry, La Trobe University, Melbourne, Victoria, Australia

Abstract

Vivax malaria is the second leading cause of malaria worldwide and the major cause of non-African malaria. Unfortunately, efforts to develop antimalarial vaccines specifically targeting Plasmodium vivax have been largely neglected, and few candidates have progressed into clinical trials. The Duffy binding protein is considered a leading blood-stage vaccine candidate because this ligand’s recognition of the Duffy blood group reticulocyte surface receptor is considered essential for infection. This study identifies a new target epitope on the ligand’s surface that may serve as the target of vaccine-induced binding-inhibitory antibody (BIAb). Understanding the potential targets of vaccine protection will be important for development of an effective vaccine.

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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