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Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b
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 P...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943553/ https://www.ncbi.nlm.nih.gov/pubmed/33750786 http://dx.doi.org/10.1038/s41467-021-21811-2 |
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author | Chan, Li-Jin Gandhirajan, Anugraha Carias, Lenore L. Dietrich, Melanie H. Vadas, Oscar Visentin, Remy França, Camila T. Menant, Sebastien Soldati-Favre, Dominique Mueller, Ivo King, Christopher L. Tham, Wai-Hong |
author_facet | Chan, Li-Jin Gandhirajan, Anugraha Carias, Lenore L. Dietrich, Melanie H. Vadas, Oscar Visentin, Remy França, Camila T. Menant, Sebastien Soldati-Favre, Dominique Mueller, Ivo King, Christopher L. Tham, Wai-Hong |
author_sort | Chan, Li-Jin |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7943553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79435532021-03-28 Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b Chan, Li-Jin Gandhirajan, Anugraha Carias, Lenore L. Dietrich, Melanie H. Vadas, Oscar Visentin, Remy França, Camila T. Menant, Sebastien Soldati-Favre, Dominique Mueller, Ivo King, Christopher L. Tham, Wai-Hong Nat Commun Article 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. Nature Publishing Group UK 2021-03-09 /pmc/articles/PMC7943553/ /pubmed/33750786 http://dx.doi.org/10.1038/s41467-021-21811-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chan, Li-Jin Gandhirajan, Anugraha Carias, Lenore L. Dietrich, Melanie H. Vadas, Oscar Visentin, Remy França, Camila T. Menant, Sebastien Soldati-Favre, Dominique Mueller, Ivo King, Christopher L. Tham, Wai-Hong Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b |
title | Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b |
title_full | Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b |
title_fullStr | Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b |
title_full_unstemmed | Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b |
title_short | Naturally acquired blocking human monoclonal antibodies to Plasmodiumvivax reticulocyte binding protein 2b |
title_sort | naturally acquired blocking human monoclonal antibodies to plasmodiumvivax reticulocyte binding protein 2b |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943553/ https://www.ncbi.nlm.nih.gov/pubmed/33750786 http://dx.doi.org/10.1038/s41467-021-21811-2 |
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