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Malaria invasion ligand RH5 and its prime candidacy in blood-stage malaria vaccine design

Journal

HUMAN VACCINES & IMMUNOTHERAPEUTICS
Volume 11, Issue 6, Pages 1465-1473

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21645515.2015.1026496

Keywords

invasion; malaria vaccine; Plasmodium falciparum; RH5; vaccine development

Funding

  1. NIAID/DMID [AI-N01-045210]

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With drug resistance to available therapeutics continuing to develop against Plasmodium falciparum malaria, the development of an effective vaccine candidate remains a major research goal. Successful interruption of invasion of parasites into erythrocytes during the blood stage of infection will prevent the severe clinical symptoms and complications associated with malaria. Previously studied blood stage antigens have highlighted the hurdles that are inherent to this life-cycle stage, namely that highly immunogenic antigens are also globally diverse, resulting in protection only against the vaccine strain, or that naturally acquired immunity to blood stage antigens do not always correlate with actual protection. The blood stage antigen reticulocyte binding homolog RH5 is essential for parasite viability, has globally limited diversity, and is associated with protection from disease. Here we summarize available information on this invasion ligand and recent findings that highlight its candidacy for inclusion in a blood-stage malaria vaccine.

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