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Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon

Circumsporozoite protein (CSP) variants of P. vivax, besides having variations in the protein repetitive portion, can differ from each other in aspects such as geographical distribution, intensity of transmission, vectorial competence and immune response. Such aspects must be considered to P. vivax...

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Autores principales: Soares, Isabela Ferreira, López-Camacho, César, Rodrigues-da-Silva, Rodrigo Nunes, da Silva Matos, Ada, de Oliveira Baptista, Barbara, Totino, Paulo Renato Rivas, de Souza, Rodrigo Medeiros, Harrison, Kate, Gimenez, Alba Marina, de Freitas, Elisângela Oliveira, Kim, Young Chan, Oliveira-Ferreira, Joseli, Daniel-Ribeiro, Cláudio Tadeu, Reyes-Sandoval, Arturo, Pratt-Riccio, Lilian Rose, Lima-Junior, Josué da Costa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441389/
https://www.ncbi.nlm.nih.gov/pubmed/32820195
http://dx.doi.org/10.1038/s41598-020-70893-3
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author Soares, Isabela Ferreira
López-Camacho, César
Rodrigues-da-Silva, Rodrigo Nunes
da Silva Matos, Ada
de Oliveira Baptista, Barbara
Totino, Paulo Renato Rivas
de Souza, Rodrigo Medeiros
Harrison, Kate
Gimenez, Alba Marina
de Freitas, Elisângela Oliveira
Kim, Young Chan
Oliveira-Ferreira, Joseli
Daniel-Ribeiro, Cláudio Tadeu
Reyes-Sandoval, Arturo
Pratt-Riccio, Lilian Rose
Lima-Junior, Josué da Costa
author_facet Soares, Isabela Ferreira
López-Camacho, César
Rodrigues-da-Silva, Rodrigo Nunes
da Silva Matos, Ada
de Oliveira Baptista, Barbara
Totino, Paulo Renato Rivas
de Souza, Rodrigo Medeiros
Harrison, Kate
Gimenez, Alba Marina
de Freitas, Elisângela Oliveira
Kim, Young Chan
Oliveira-Ferreira, Joseli
Daniel-Ribeiro, Cláudio Tadeu
Reyes-Sandoval, Arturo
Pratt-Riccio, Lilian Rose
Lima-Junior, Josué da Costa
author_sort Soares, Isabela Ferreira
collection PubMed
description Circumsporozoite protein (CSP) variants of P. vivax, besides having variations in the protein repetitive portion, can differ from each other in aspects such as geographical distribution, intensity of transmission, vectorial competence and immune response. Such aspects must be considered to P. vivax vaccine development. Therefore, we evaluated the immunogenicity of novel recombinant proteins corresponding to each of the three P. vivax allelic variants (VK210, VK247 and P. vivax-like) and of the C-terminal region (shared by all PvCSP variants) in naturally malaria-exposed populations of Brazilian Amazon. Our results demonstrated that PvCSP-VK210 was the major target of humoral immune response in studied population, presenting higher frequency and magnitude of IgG response. The IgG subclass profile showed a prevalence of cytophilic antibodies (IgG1 and IgG3), that seem to have an essential role in protective immune response. Differently of PvCSP allelic variants, antibodies elicited against C-terminal region of protein did not correlate with epidemiological parameters, bringing additional evidence that humoral response against this protein region is not essential to protective immunity. Taken together, these findings increase the knowledge on serological response to distinct PvCSP allelic variants and may contribute to the development of a global and effective P. vivax vaccine.
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spelling pubmed-74413892020-08-26 Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon Soares, Isabela Ferreira López-Camacho, César Rodrigues-da-Silva, Rodrigo Nunes da Silva Matos, Ada de Oliveira Baptista, Barbara Totino, Paulo Renato Rivas de Souza, Rodrigo Medeiros Harrison, Kate Gimenez, Alba Marina de Freitas, Elisângela Oliveira Kim, Young Chan Oliveira-Ferreira, Joseli Daniel-Ribeiro, Cláudio Tadeu Reyes-Sandoval, Arturo Pratt-Riccio, Lilian Rose Lima-Junior, Josué da Costa Sci Rep Article Circumsporozoite protein (CSP) variants of P. vivax, besides having variations in the protein repetitive portion, can differ from each other in aspects such as geographical distribution, intensity of transmission, vectorial competence and immune response. Such aspects must be considered to P. vivax vaccine development. Therefore, we evaluated the immunogenicity of novel recombinant proteins corresponding to each of the three P. vivax allelic variants (VK210, VK247 and P. vivax-like) and of the C-terminal region (shared by all PvCSP variants) in naturally malaria-exposed populations of Brazilian Amazon. Our results demonstrated that PvCSP-VK210 was the major target of humoral immune response in studied population, presenting higher frequency and magnitude of IgG response. The IgG subclass profile showed a prevalence of cytophilic antibodies (IgG1 and IgG3), that seem to have an essential role in protective immune response. Differently of PvCSP allelic variants, antibodies elicited against C-terminal region of protein did not correlate with epidemiological parameters, bringing additional evidence that humoral response against this protein region is not essential to protective immunity. Taken together, these findings increase the knowledge on serological response to distinct PvCSP allelic variants and may contribute to the development of a global and effective P. vivax vaccine. Nature Publishing Group UK 2020-08-20 /pmc/articles/PMC7441389/ /pubmed/32820195 http://dx.doi.org/10.1038/s41598-020-70893-3 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Soares, Isabela Ferreira
López-Camacho, César
Rodrigues-da-Silva, Rodrigo Nunes
da Silva Matos, Ada
de Oliveira Baptista, Barbara
Totino, Paulo Renato Rivas
de Souza, Rodrigo Medeiros
Harrison, Kate
Gimenez, Alba Marina
de Freitas, Elisângela Oliveira
Kim, Young Chan
Oliveira-Ferreira, Joseli
Daniel-Ribeiro, Cláudio Tadeu
Reyes-Sandoval, Arturo
Pratt-Riccio, Lilian Rose
Lima-Junior, Josué da Costa
Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon
title Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon
title_full Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon
title_fullStr Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon
title_full_unstemmed Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon
title_short Recombinant Plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the Brazilian Amazon
title_sort recombinant plasmodium vivax circumsporozoite surface protein allelic variants: antibody recognition by individuals from three communities in the brazilian amazon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441389/
https://www.ncbi.nlm.nih.gov/pubmed/32820195
http://dx.doi.org/10.1038/s41598-020-70893-3
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