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

Author:

Baptista Barbara de Oliveira12ORCID,Souza Ana Beatriz Lopes de12,Oliveira Luana Santos de12,Souza Hugo Amorim dos Santos de12ORCID,Barros Jenifer Peixoto de12,Queiroz Lucas Tavares de12,Souza Rodrigo Medeiros de3ORCID,Amoah Linda Eva4ORCID,Singh Susheel Kumar56ORCID,Theisen Michael56,Rodrigues-da-Silva Rodrigo Nunes7ORCID,Riccio Evelyn Kety Pratt12,Totino Paulo Renato Rivas12,Lima-Junior Josué da Costa8,Daniel-Ribeiro Cláudio Tadeu12ORCID,Pratt-Riccio Lilian Rose12ORCID

Affiliation:

1. Laboratório de Pesquisa em Malária, Instituto Oswaldo Cruz (IOC), Fundação Oswaldo Cruz (Fiocruz), Rio de Janeiro 21040-900, RJ, Brazil

2. Centro de Pesquisa, Diagnóstico e Treinamento em Malária (CPD-Mal), Fiocruz e Secretaria de Vigilância em Saúde, Ministério da Saúde, Rio de Janeiro 21040-900, RJ, Brazil

3. Centro de Pesquisa em Doenças Infecciosas, Universidade Federal do Acre–Campus Floresta (UFAC), Cruzeiro do Sul 69895-000, AC, Brazil

4. Immunology Department, Noguchi Memorial Institute for Medical Research, University of Ghana, Accra P.O. Box LG 25, Ghana

5. Centre for Medical Parasitology, Department of International Health, Immunology and Microbiology, University of Copenhagen, DK-2200 Copenhagen, Denmark

6. Department of Infectious Disease, Copenhagen University Hospital, DK-2200 Copenhagen, Denmark

7. Laboratório de Tecnologia Imunológica, Instituto de Tecnologia em Imunobiológicos (Bio-Manguinhos), Fiocruz, Rio de Janeiro 21040-900, RJ, Brazil

8. Laboratório de Imunoparasitologia, IOC, Fiocruz, Rio de Janeiro 21040-900, RJ, Brazil

Abstract

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.

Funder

Fundação Oswaldo Cruz

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brazil

(INCT-NIM/CNPq)

Rede de Neuroinflamação

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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