Naturally acquired antibodies to Plasmodium vivax blood-stage vaccine candidates (PvMSP-1(19) and PvMSP-3 alpha(359-798)) and their relationship with hematological features in malaria patients from the Brazilian Amazon


Autoria(s): Mourao, Luiza Carvalho; Morais, Cristiane Guimaraes; Bueno, Lilian Lacerda; Jimenez, Maria Carolina; Soares, Irene da Silva; Fontes, Cor Jesus; Lacerda, Marcus Vinicius Guimaraes; Xavier, Marcos Silva; Barnwell, John W.; Galinski, Mary R.; Braga, Erika Martins
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

21/10/2013

21/10/2013

2012

Resumo

An important step when designing a vaccine is identifying the antigens that function as targets of naturally acquired antibodies. We investigated specific antibody responses against two Plasmodium vivax vaccine candidates, PvMSP-1(19) and PvMSP-3 alpha(359-798). Moreover, we assessed the relationship between these antibodies and morbidity parameters. PvMSP-1(19) was the most immunogenic antigen and the frequency of responders to this protein tended to increase in P. vivax patients with higher parasitemia. For both antigens, IgG antibody responses tended to be lower in patients who had experienced their first bout of malaria. Furthermore, anemic patients presented higher IgG antibody responses to PvMSP-3 alpha(359-798). Since the humoral response involves a number of antibodies acting simultaneously on different targets, we performed a Principal Component Analysis (PCA). Anemic patients had, on average, higher first principal component scores (IgG1/IgG2/IgG3/IgG4 anti-MSP3 alpha), which were negatively correlated with hemoglobin levels. Since antibodies against PfMSP-3 have been strongly associated with clinical protection, we cannot exclude the possibility of a dual role of PvMSP-3 specific antibodies in both immunity and pathogenesis of vivax malaria. Our results confirm the high immunogenicity of the conserved C terminus of PvMSP-1 and points to the considerable immunogenicity of polymorphic PvMSP-3 alpha(359-798) during natural infection. (C) 2012 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.

CNPq

CNPq

Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG)

Fundacao de Amparo a Pesquisa do Estado de Minas Gerais/FAPEMIG [CBB PPM-0003-09 e CBB - PPM-00177-11]

Conselho Nacional de Pesquisa (CNPq, Brazil)

Conselho Nacional de Pesquisa (CNPq/Brazil) [471156/2010-8]

Pronex Malaria, DECIT/MS [555646/2009-2]

Pronex Malaria, DECIT/MS

Identificador

MICROBES AND INFECTION, AMSTERDAM, v. 14, n. 9, p. 730-739, AUG, 2012

1286-4579

http://www.producao.usp.br/handle/BDPI/35198

10.1016/j.micinf.2012.02.011

http://dx.doi.org/10.1016/j.micinf.2012.02.011

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

AMSTERDAM

Relação

MICROBES AND INFECTION

Direitos

closedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #PLASMODIUM VIVAX #MEROZOITE ANTIGENS #MALARIA VACCINE #ANTIBODIES #MEROZOITE SURFACE PROTEIN-1 #PAPUA-NEW-GUINEA #FALCIPARUM MALARIA #19 KDA #RESPONSES #PARASITE #ANEMIA #IGG #CHILDREN #TRANSMISSION #IMMUNOLOGY #INFECTIOUS DISEASES #MICROBIOLOGY
Tipo

article

original article

publishedVersion