Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in mice
Abstract Human malaria affects the vast majority of the world’s population with the Plasmodium falciparum species causing the highest rates of morbidity and mortality. With no licensed vaccine and leading candidates achieving suboptimal protection in the field, the need for an effective immunoprophy...
| Published in: | npj Vaccines |
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| Main Authors: | , , , , , , , , , , , , , , , , |
| Format: | Article |
| Language: | English |
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Nature Portfolio
2021-06-01
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| Online Access: | https://doi.org/10.1038/s41541-021-00345-0 |
| _version_ | 1852662374656376832 |
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| author | Katherine L. Mallory Justin A. Taylor Xiaoyan Zou Ishita N. Waghela Cosette G. Schneider Michael Q. Sibilo Neeraja M. Punde Leah C. Perazzo Tatyana Savransky Martha Sedegah Sheetij Dutta Chris J. Janse Norbert Pardi Paulo J. C. Lin Ying K. Tam Drew Weissman Evelina Angov |
| author_facet | Katherine L. Mallory Justin A. Taylor Xiaoyan Zou Ishita N. Waghela Cosette G. Schneider Michael Q. Sibilo Neeraja M. Punde Leah C. Perazzo Tatyana Savransky Martha Sedegah Sheetij Dutta Chris J. Janse Norbert Pardi Paulo J. C. Lin Ying K. Tam Drew Weissman Evelina Angov |
| author_sort | Katherine L. Mallory |
| collection | DOAJ |
| container_title | npj Vaccines |
| description | Abstract Human malaria affects the vast majority of the world’s population with the Plasmodium falciparum species causing the highest rates of morbidity and mortality. With no licensed vaccine and leading candidates achieving suboptimal protection in the field, the need for an effective immunoprophylactic option continues to motivate the malaria research community to explore alternative technologies. Recent advances in the mRNA discipline have elevated the long-neglected platform to the forefront of infectious disease research. As the immunodominant coat protein of the invasive stage of the malaria parasite, circumsporozoite protein (PfCSP) was selected as the antigen of choice to assess the immunogenic and protective potential of an mRNA malaria vaccine. In mammalian cell transfection experiments, PfCSP mRNA was well expressed and cell associated. In the transition to an in vivo murine model, lipid nanoparticle (LNP) encapsulation was applied to protect and deliver the mRNA to the cell translation machinery and supply adjuvant activity. The immunogenic effect of an array of factors was explored, such as formulation, dose, number, and interval of immunizations. PfCSP mRNA-LNP achieved sterile protection against infection with two P. berghei PfCSP transgenic parasite strains, with mRNA dose and vaccination interval having a greater effect on outcome. This investigation serves as the assessment of pre-erythrocytic malaria, PfCSP mRNA vaccine candidate resulting in sterile protection, with numerous factors affecting protective efficacy, making it a compelling candidate for further investigation. |
| format | Article |
| id | doaj-art-e05bb1dcc8a24bf8950c79ee7ff517fc |
| institution | Directory of Open Access Journals |
| issn | 2059-0105 |
| language | English |
| publishDate | 2021-06-01 |
| publisher | Nature Portfolio |
| record_format | Article |
| spelling | doaj-art-e05bb1dcc8a24bf8950c79ee7ff517fc2025-08-19T21:36:20ZengNature Portfolionpj Vaccines2059-01052021-06-016111210.1038/s41541-021-00345-0Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in miceKatherine L. Mallory0Justin A. Taylor1Xiaoyan Zou2Ishita N. Waghela3Cosette G. Schneider4Michael Q. Sibilo5Neeraja M. Punde6Leah C. Perazzo7Tatyana Savransky8Martha Sedegah9Sheetij Dutta10Chris J. Janse11Norbert Pardi12Paulo J. C. Lin13Ying K. Tam14Drew Weissman15Evelina Angov16Walter Reed Army Institute of ResearchWalter Reed Army Institute of ResearchNaval Medical Research CenterWalter Reed Army Institute of ResearchWalter Reed Army Institute of ResearchWalter Reed Army Institute of ResearchWalter Reed Army Institute of ResearchWalter Reed Army Institute of ResearchWalter Reed Army Institute of ResearchNaval Medical Research CenterWalter Reed Army Institute of ResearchLeiden University Medical CenterUniversity of PennsylvaniaAcuitas TherapeuticsAcuitas TherapeuticsUniversity of PennsylvaniaWalter Reed Army Institute of ResearchAbstract Human malaria affects the vast majority of the world’s population with the Plasmodium falciparum species causing the highest rates of morbidity and mortality. With no licensed vaccine and leading candidates achieving suboptimal protection in the field, the need for an effective immunoprophylactic option continues to motivate the malaria research community to explore alternative technologies. Recent advances in the mRNA discipline have elevated the long-neglected platform to the forefront of infectious disease research. As the immunodominant coat protein of the invasive stage of the malaria parasite, circumsporozoite protein (PfCSP) was selected as the antigen of choice to assess the immunogenic and protective potential of an mRNA malaria vaccine. In mammalian cell transfection experiments, PfCSP mRNA was well expressed and cell associated. In the transition to an in vivo murine model, lipid nanoparticle (LNP) encapsulation was applied to protect and deliver the mRNA to the cell translation machinery and supply adjuvant activity. The immunogenic effect of an array of factors was explored, such as formulation, dose, number, and interval of immunizations. PfCSP mRNA-LNP achieved sterile protection against infection with two P. berghei PfCSP transgenic parasite strains, with mRNA dose and vaccination interval having a greater effect on outcome. This investigation serves as the assessment of pre-erythrocytic malaria, PfCSP mRNA vaccine candidate resulting in sterile protection, with numerous factors affecting protective efficacy, making it a compelling candidate for further investigation.https://doi.org/10.1038/s41541-021-00345-0 |
| spellingShingle | Katherine L. Mallory Justin A. Taylor Xiaoyan Zou Ishita N. Waghela Cosette G. Schneider Michael Q. Sibilo Neeraja M. Punde Leah C. Perazzo Tatyana Savransky Martha Sedegah Sheetij Dutta Chris J. Janse Norbert Pardi Paulo J. C. Lin Ying K. Tam Drew Weissman Evelina Angov Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in mice |
| title | Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in mice |
| title_full | Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in mice |
| title_fullStr | Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in mice |
| title_full_unstemmed | Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in mice |
| title_short | Messenger RNA expressing PfCSP induces functional, protective immune responses against malaria in mice |
| title_sort | messenger rna expressing pfcsp induces functional protective immune responses against malaria in mice |
| url | https://doi.org/10.1038/s41541-021-00345-0 |
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