| Literature DB >> 33750786 |
Li-Jin Chan1,2, Anugraha Gandhirajan3, Lenore L Carias3, Melanie H Dietrich1, Oscar Vadas4,5, Remy Visentin4,5, Camila T França1,2, Sebastien Menant1, Dominique Soldati-Favre4, Ivo Mueller1,2, Christopher L King6,7, Wai-Hong Tham8,9.
Abstract
Plasmodium vivax preferentially invades reticulocytes and recognition of these cells is mediated by P. vivax Reticulocyte Binding Protein 2b (PvRBP2b) binding to human Transferrin receptor 1 (TfR1) and Transferrin (Tf). Longitudinal cohort studies in Papua New Guinea, Thailand and Brazil show that PvRBP2b antibodies are correlated with protection against P. vivax infection and disease. Here, we isolate and characterize anti-PvRBP2b human monoclonal antibodies from two individuals in Cambodia with natural P. vivax infection. These antibodies bind with high affinities and map to different regions of PvRBP2b. Several human antibodies block PvRBP2b binding to reticulocytes and inhibit complex formation with human TfR1-Tf. We describe different structural mechanisms for functional inhibition, including either steric hindrance with TfR1-Tf or the reticulocyte membrane. These results show that naturally acquired human antibodies against PvRBP2b can inhibit its function which is important for P. vivax invasion.Entities:
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Year: 2021 PMID: 33750786 PMCID: PMC7943553 DOI: 10.1038/s41467-021-21811-2
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919