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Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2

MSP2 is an intrinsically disordered protein that is abundant on the merozoite surface and essential to the parasite Plasmodium falciparum. Naturally-acquired antibody responses to MSP2 are biased towards dimorphic sequences within the central variable region of MSP2 and have been linked to naturally...

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Autores principales: Krishnarjuna, Bankala, Andrew, Dean, MacRaild, Christopher A., Morales, Rodrigo A. V., Beeson, James G., Anders, Robin F., Richards, Jack S., Norton, Raymond S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749986/
https://www.ncbi.nlm.nih.gov/pubmed/26865062
http://dx.doi.org/10.1038/srep20613
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author Krishnarjuna, Bankala
Andrew, Dean
MacRaild, Christopher A.
Morales, Rodrigo A. V.
Beeson, James G.
Anders, Robin F.
Richards, Jack S.
Norton, Raymond S.
author_facet Krishnarjuna, Bankala
Andrew, Dean
MacRaild, Christopher A.
Morales, Rodrigo A. V.
Beeson, James G.
Anders, Robin F.
Richards, Jack S.
Norton, Raymond S.
author_sort Krishnarjuna, Bankala
collection PubMed
description MSP2 is an intrinsically disordered protein that is abundant on the merozoite surface and essential to the parasite Plasmodium falciparum. Naturally-acquired antibody responses to MSP2 are biased towards dimorphic sequences within the central variable region of MSP2 and have been linked to naturally-acquired protection from malaria. In a phase IIb study, an MSP2-containing vaccine induced an immune response that reduced parasitemias in a strain-specific manner. A subsequent phase I study of a vaccine that contained both dimorphic forms of MSP2 induced antibodies that exhibited functional activity in vitro. We have assessed the contribution of the conserved and variable regions of MSP2 to the generation of a strain-transcending antibody response by generating MSP2 chimeras that included conserved and variable regions of the 3D7 and FC27 alleles. Robust anti-MSP2 antibody responses targeting both conserved and variable regions were generated in mice, although the fine specificity and the balance of responses to these regions differed amongst the constructs tested. We observed significant differences in antibody subclass distribution in the responses to these chimeras. Our results suggest that chimeric MSP2 antigens can elicit a broad immune response suitable for protection against different strains of P. falciparum.
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spelling pubmed-47499862016-02-18 Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2 Krishnarjuna, Bankala Andrew, Dean MacRaild, Christopher A. Morales, Rodrigo A. V. Beeson, James G. Anders, Robin F. Richards, Jack S. Norton, Raymond S. Sci Rep Article MSP2 is an intrinsically disordered protein that is abundant on the merozoite surface and essential to the parasite Plasmodium falciparum. Naturally-acquired antibody responses to MSP2 are biased towards dimorphic sequences within the central variable region of MSP2 and have been linked to naturally-acquired protection from malaria. In a phase IIb study, an MSP2-containing vaccine induced an immune response that reduced parasitemias in a strain-specific manner. A subsequent phase I study of a vaccine that contained both dimorphic forms of MSP2 induced antibodies that exhibited functional activity in vitro. We have assessed the contribution of the conserved and variable regions of MSP2 to the generation of a strain-transcending antibody response by generating MSP2 chimeras that included conserved and variable regions of the 3D7 and FC27 alleles. Robust anti-MSP2 antibody responses targeting both conserved and variable regions were generated in mice, although the fine specificity and the balance of responses to these regions differed amongst the constructs tested. We observed significant differences in antibody subclass distribution in the responses to these chimeras. Our results suggest that chimeric MSP2 antigens can elicit a broad immune response suitable for protection against different strains of P. falciparum. Nature Publishing Group 2016-02-11 /pmc/articles/PMC4749986/ /pubmed/26865062 http://dx.doi.org/10.1038/srep20613 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Krishnarjuna, Bankala
Andrew, Dean
MacRaild, Christopher A.
Morales, Rodrigo A. V.
Beeson, James G.
Anders, Robin F.
Richards, Jack S.
Norton, Raymond S.
Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2
title Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2
title_full Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2
title_fullStr Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2
title_full_unstemmed Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2
title_short Strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2
title_sort strain-transcending immune response generated by chimeras of the malaria vaccine candidate merozoite surface protein 2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749986/
https://www.ncbi.nlm.nih.gov/pubmed/26865062
http://dx.doi.org/10.1038/srep20613
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