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B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon

The GMZ2.6c malaria vaccine candidate is a multi-stage P. falciparum chimeric protein that contains a fragment of the sexual-stage Pfs48/45-6C protein genetically fused to GMZ2, an asexual-stage vaccine construction consisting of the N-terminal region of the glutamate-rich protein (GLURP) and the C-...

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Autores principales: Baptista, Barbara de Oliveira, de Souza, Ana Beatriz Lopes, de Oliveira, Luana Santos, de Souza, Hugo Amorim dos Santos, de Barros, Jenifer Peixoto, de Queiroz, Lucas Tavares, de Souza, Rodrigo Medeiros, Amoah, Linda Eva, Singh, Susheel Kumar, Theisen, Michael, Rodrigues-da-Silva, Rodrigo Nunes, Riccio, Evelyn Kety Pratt, Totino, Paulo Renato Rivas, Lima-Junior, Josué da Costa, Daniel-Ribeiro, Cláudio Tadeu, Pratt-Riccio, Lilian Rose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966924/
https://www.ncbi.nlm.nih.gov/pubmed/36851323
http://dx.doi.org/10.3390/vaccines11020446
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author Baptista, Barbara de Oliveira
de Souza, Ana Beatriz Lopes
de Oliveira, Luana Santos
de Souza, Hugo Amorim dos Santos
de Barros, Jenifer Peixoto
de Queiroz, Lucas Tavares
de Souza, Rodrigo Medeiros
Amoah, Linda Eva
Singh, Susheel Kumar
Theisen, Michael
Rodrigues-da-Silva, Rodrigo Nunes
Riccio, Evelyn Kety Pratt
Totino, Paulo Renato Rivas
Lima-Junior, Josué da Costa
Daniel-Ribeiro, Cláudio Tadeu
Pratt-Riccio, Lilian Rose
author_facet Baptista, Barbara de Oliveira
de Souza, Ana Beatriz Lopes
de Oliveira, Luana Santos
de Souza, Hugo Amorim dos Santos
de Barros, Jenifer Peixoto
de Queiroz, Lucas Tavares
de Souza, Rodrigo Medeiros
Amoah, Linda Eva
Singh, Susheel Kumar
Theisen, Michael
Rodrigues-da-Silva, Rodrigo Nunes
Riccio, Evelyn Kety Pratt
Totino, Paulo Renato Rivas
Lima-Junior, Josué da Costa
Daniel-Ribeiro, Cláudio Tadeu
Pratt-Riccio, Lilian Rose
author_sort Baptista, Barbara de Oliveira
collection PubMed
description The GMZ2.6c malaria vaccine candidate is a multi-stage P. falciparum chimeric protein that contains a fragment of the sexual-stage Pfs48/45-6C protein genetically fused to GMZ2, an asexual-stage vaccine construction consisting of the N-terminal region of the glutamate-rich protein (GLURP) and the C-terminal region of the merozoite surface protein-3 (MSP-3). Previous studies showed that GMZ2.6c is widely recognized by antibodies from Brazilian exposed individuals and that its components are immunogenic in natural infection by P. falciparum. In addition, anti-GMZ2.6c antibodies increase with exposure to infection and may contribute to parasite immunity. Therefore, identifying epitopes of proteins recognized by antibodies may be an important tool for understanding protective immunity. Herein, we identify and validate the B-cell epitopes of GMZ2.6c as immunogenic and immunodominant in individuals exposed to malaria living in endemic areas of the Brazilian Amazon. Specific IgG antibodies and subclasses against MSP-3, GLURP, and Pfs48/45 epitopes were detected by ELISA using synthetic peptides corresponding to B-cell epitopes previously described for MSP-3 and GLURP or identified by BepiPred for Pfs48/45. The results showed that the immunodominant epitopes were P11 from GLURP and MSP-3c and DG210 from MSP-3. The IgG1 and IgG3 subclasses were preferentially induced against these epitopes, supporting previous studies that these proteins are targets for cytophilic antibodies, important for the acquisition of protective immunity. Most individuals presented detectable IgG antibodies against Pfs48/45a and/or Pfs48/45b, validating the prediction of linear B-cell epitopes. The higher frequency and antibody levels against different epitopes from GLURP, MSP-3, and Pfs48/45 provide additional information that may suggest the relevance of GMZ2.6c as a multi-stage malaria vaccine candidate.
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spelling pubmed-99669242023-02-26 B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon Baptista, Barbara de Oliveira de Souza, Ana Beatriz Lopes de Oliveira, Luana Santos de Souza, Hugo Amorim dos Santos de Barros, Jenifer Peixoto de Queiroz, Lucas Tavares de Souza, Rodrigo Medeiros Amoah, Linda Eva Singh, Susheel Kumar Theisen, Michael Rodrigues-da-Silva, Rodrigo Nunes Riccio, Evelyn Kety Pratt Totino, Paulo Renato Rivas Lima-Junior, Josué da Costa Daniel-Ribeiro, Cláudio Tadeu Pratt-Riccio, Lilian Rose Vaccines (Basel) Article The GMZ2.6c malaria vaccine candidate is a multi-stage P. falciparum chimeric protein that contains a fragment of the sexual-stage Pfs48/45-6C protein genetically fused to GMZ2, an asexual-stage vaccine construction consisting of the N-terminal region of the glutamate-rich protein (GLURP) and the C-terminal region of the merozoite surface protein-3 (MSP-3). Previous studies showed that GMZ2.6c is widely recognized by antibodies from Brazilian exposed individuals and that its components are immunogenic in natural infection by P. falciparum. In addition, anti-GMZ2.6c antibodies increase with exposure to infection and may contribute to parasite immunity. Therefore, identifying epitopes of proteins recognized by antibodies may be an important tool for understanding protective immunity. Herein, we identify and validate the B-cell epitopes of GMZ2.6c as immunogenic and immunodominant in individuals exposed to malaria living in endemic areas of the Brazilian Amazon. Specific IgG antibodies and subclasses against MSP-3, GLURP, and Pfs48/45 epitopes were detected by ELISA using synthetic peptides corresponding to B-cell epitopes previously described for MSP-3 and GLURP or identified by BepiPred for Pfs48/45. The results showed that the immunodominant epitopes were P11 from GLURP and MSP-3c and DG210 from MSP-3. The IgG1 and IgG3 subclasses were preferentially induced against these epitopes, supporting previous studies that these proteins are targets for cytophilic antibodies, important for the acquisition of protective immunity. Most individuals presented detectable IgG antibodies against Pfs48/45a and/or Pfs48/45b, validating the prediction of linear B-cell epitopes. The higher frequency and antibody levels against different epitopes from GLURP, MSP-3, and Pfs48/45 provide additional information that may suggest the relevance of GMZ2.6c as a multi-stage malaria vaccine candidate. MDPI 2023-02-15 /pmc/articles/PMC9966924/ /pubmed/36851323 http://dx.doi.org/10.3390/vaccines11020446 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Baptista, Barbara de Oliveira
de Souza, Ana Beatriz Lopes
de Oliveira, Luana Santos
de Souza, Hugo Amorim dos Santos
de Barros, Jenifer Peixoto
de Queiroz, Lucas Tavares
de Souza, Rodrigo Medeiros
Amoah, Linda Eva
Singh, Susheel Kumar
Theisen, Michael
Rodrigues-da-Silva, Rodrigo Nunes
Riccio, Evelyn Kety Pratt
Totino, Paulo Renato Rivas
Lima-Junior, Josué da Costa
Daniel-Ribeiro, Cláudio Tadeu
Pratt-Riccio, Lilian Rose
B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon
title B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon
title_full B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon
title_fullStr B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon
title_full_unstemmed B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon
title_short B-Cell Epitope Mapping of the Plasmodium falciparum Malaria Vaccine Candidate GMZ2.6c in a Naturally Exposed Population of the Brazilian Amazon
title_sort b-cell epitope mapping of the plasmodium falciparum malaria vaccine candidate gmz2.6c in a naturally exposed population of the brazilian amazon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966924/
https://www.ncbi.nlm.nih.gov/pubmed/36851323
http://dx.doi.org/10.3390/vaccines11020446
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