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Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein
Combinations of monoclonal antibodies (mAbs) against different epitopes on the same antigen synergistically neutralize many viruses. However, there are limited studies assessing whether combining human mAbs against distinct regions of the Plasmodium falciparum (Pf) circumsporozoite protein (CSP) enh...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675929/ https://www.ncbi.nlm.nih.gov/pubmed/34871332 http://dx.doi.org/10.1371/journal.ppat.1010133 |
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author | Wang, Lawrence T. Pereira, Lais S. Kiyuka, Patience K. Schön, Arne Kisalu, Neville K. Vistein, Rachel Dillon, Marlon Bonilla, Brian G. Molina-Cruz, Alvaro Barillas-Mury, Carolina Tan, Joshua Idris, Azza H. Francica, Joseph R. Seder, Robert A. |
author_facet | Wang, Lawrence T. Pereira, Lais S. Kiyuka, Patience K. Schön, Arne Kisalu, Neville K. Vistein, Rachel Dillon, Marlon Bonilla, Brian G. Molina-Cruz, Alvaro Barillas-Mury, Carolina Tan, Joshua Idris, Azza H. Francica, Joseph R. Seder, Robert A. |
author_sort | Wang, Lawrence T. |
collection | PubMed |
description | Combinations of monoclonal antibodies (mAbs) against different epitopes on the same antigen synergistically neutralize many viruses. However, there are limited studies assessing whether combining human mAbs against distinct regions of the Plasmodium falciparum (Pf) circumsporozoite protein (CSP) enhances in vivo protection against malaria compared to each mAb alone or whether passive transfer of PfCSP mAbs would improve protection following vaccination against PfCSP. Here, we isolated a panel of human mAbs against the subdominant C-terminal domain of PfCSP (C-CSP) from a volunteer immunized with radiation-attenuated Pf sporozoites. These C-CSP-specific mAbs had limited binding to sporozoites in vitro that was increased by combination with neutralizing human “repeat” mAbs against the NPDP/NVDP/NANP tetrapeptides in the central repeat region of PfCSP. Nevertheless, passive transfer of repeat- and C-CSP-specific mAb combinations did not provide enhanced protection against in vivo sporozoite challenge compared to repeat mAbs alone. Furthermore, combining potent repeat-specific mAbs (CIS43, L9, and 317) that respectively target the three tetrapeptides (NPDP/NVDP/NANP) did not provide additional protection against in vivo sporozoite challenge. However, administration of either CIS43, L9, or 317 (but not C-CSP-specific mAbs) to mice that had been immunized with R21, a PfCSP-based virus-like particle vaccine that induces polyclonal antibodies against the repeat region and C-CSP, provided enhanced protection against sporozoite challenge when compared to vaccine or mAbs alone. Collectively, this study shows that while combining mAbs against the repeat and C-terminal regions of PfCSP provide no additional protection in vivo, repeat mAbs do provide increased protection when combined with vaccine-induced polyclonal antibodies. These data should inform the implementation of PfCSP human mAbs alone or following vaccination to prevent malaria infection. |
format | Online Article Text |
id | pubmed-8675929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-86759292021-12-17 Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein Wang, Lawrence T. Pereira, Lais S. Kiyuka, Patience K. Schön, Arne Kisalu, Neville K. Vistein, Rachel Dillon, Marlon Bonilla, Brian G. Molina-Cruz, Alvaro Barillas-Mury, Carolina Tan, Joshua Idris, Azza H. Francica, Joseph R. Seder, Robert A. PLoS Pathog Research Article Combinations of monoclonal antibodies (mAbs) against different epitopes on the same antigen synergistically neutralize many viruses. However, there are limited studies assessing whether combining human mAbs against distinct regions of the Plasmodium falciparum (Pf) circumsporozoite protein (CSP) enhances in vivo protection against malaria compared to each mAb alone or whether passive transfer of PfCSP mAbs would improve protection following vaccination against PfCSP. Here, we isolated a panel of human mAbs against the subdominant C-terminal domain of PfCSP (C-CSP) from a volunteer immunized with radiation-attenuated Pf sporozoites. These C-CSP-specific mAbs had limited binding to sporozoites in vitro that was increased by combination with neutralizing human “repeat” mAbs against the NPDP/NVDP/NANP tetrapeptides in the central repeat region of PfCSP. Nevertheless, passive transfer of repeat- and C-CSP-specific mAb combinations did not provide enhanced protection against in vivo sporozoite challenge compared to repeat mAbs alone. Furthermore, combining potent repeat-specific mAbs (CIS43, L9, and 317) that respectively target the three tetrapeptides (NPDP/NVDP/NANP) did not provide additional protection against in vivo sporozoite challenge. However, administration of either CIS43, L9, or 317 (but not C-CSP-specific mAbs) to mice that had been immunized with R21, a PfCSP-based virus-like particle vaccine that induces polyclonal antibodies against the repeat region and C-CSP, provided enhanced protection against sporozoite challenge when compared to vaccine or mAbs alone. Collectively, this study shows that while combining mAbs against the repeat and C-terminal regions of PfCSP provide no additional protection in vivo, repeat mAbs do provide increased protection when combined with vaccine-induced polyclonal antibodies. These data should inform the implementation of PfCSP human mAbs alone or following vaccination to prevent malaria infection. Public Library of Science 2021-12-06 /pmc/articles/PMC8675929/ /pubmed/34871332 http://dx.doi.org/10.1371/journal.ppat.1010133 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Wang, Lawrence T. Pereira, Lais S. Kiyuka, Patience K. Schön, Arne Kisalu, Neville K. Vistein, Rachel Dillon, Marlon Bonilla, Brian G. Molina-Cruz, Alvaro Barillas-Mury, Carolina Tan, Joshua Idris, Azza H. Francica, Joseph R. Seder, Robert A. Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein |
title | Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein |
title_full | Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein |
title_fullStr | Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein |
title_full_unstemmed | Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein |
title_short | Protective effects of combining monoclonal antibodies and vaccines against the Plasmodium falciparum circumsporozoite protein |
title_sort | protective effects of combining monoclonal antibodies and vaccines against the plasmodium falciparum circumsporozoite protein |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675929/ https://www.ncbi.nlm.nih.gov/pubmed/34871332 http://dx.doi.org/10.1371/journal.ppat.1010133 |
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