4.8 Article

Transferrin receptor 1 is a reticulocyte-specific receptor for Plasmodium vivax

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SCIENCE
卷 359, 期 6371, 页码 48-+

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aan1078

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资金

  1. Howard Hughes Medical Institute-Wellcome Trust International Research Scholar [208693/Z/17/Z]
  2. Australian Research Council Future Fellowships
  3. Speedy Innovation Grant
  4. National Health and Medical Research Council fellowship [1105754]
  5. Canadian Institutes of Health Research Postdoctoral Fellowship
  6. Wellcome Trust [090770]
  7. Wellcome Trust Senior Clinical Research Fellowship [108070/Z/15/Z]
  8. Singapore National Medical Research Council (NMRC) [NMRC/CBRG/0047/2013]
  9. Agency for Science, Technology and Research (A*STAR, Singapore)
  10. Wellcome Trust of Great Britain as part of the Oxford Tropical Medicine Research Programme of Wellcome Trust-Mahidol University
  11. National Institutes of Health [1R01HL139337]
  12. Marsden Fund [17-UOO-241]
  13. Wellcome Trust Sanger Institute [Wellcome Trust 206194, 098051]

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Plasmodium vivax shows a strict host tropism for reticulocytes. We identified transferrin receptor 1 (TfR1) as the receptor for P. vivax reticulocyte-binding protein 2b (PvRBP2b). We determined the structure of the N-terminal domain of PvRBP2b involved in red blood cell binding, elucidating the molecular basis for TfR1 recognition. We validated TfR1 as the biological target of PvRBP2b engagement by means of TfR1 expression knockdown analysis. TfR1 mutant cells deficient in PvRBP2b binding were refractory to invasion of P. vivax but not to invasion of P. falciparum. Using Brazilian and Thai clinical isolates, we show that PvRBP2b monoclonal antibodies that inhibit reticulocyte binding also block P. vivax entry into reticulocytes. These data show that TfR1-PvRBP2b invasion pathway is critical for the recognition of reticulocytes during P. vivax invasion.

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