New malaria vaccine candidates based on the Plasmodium vivax Merozoite Surface Protein-1 and the TLR-5 agonist Salmonella Typhimurium FliC flagellin


Autoria(s): BARGIERI, Daniel Y.; ROSA, Daniela S.; BRAGA, Catarina J. M.; CARVALHO, Bruna O.; COSTA, Fabio T. M.; ESPINDOLA, Noeli Maria; VAZ, Adelaide Jose; SOARES, Irene S.; FERREIRA, Luis C. S.; RODRIGUES, Mauricio M.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

The present study evaluated the immunogenicity of new malaria vaccine formulations based on the 19 kDa C-terminal fragment of Plasmodium vivax Merozoite Surface Protein-1 (MSP1(19)) and the Salmonella enterica serovar Typhimurium flagellin (FIiC), a Toll-like receptor 5 (TLR5) agonist. FHC was used as an adjuvant either admixed or genetically linked to the P. vivax MSP1(19) and administered to C57BL/6 mice via parenteral (s.c.) or mucosal (i.n.) routes. The recombinant fusion protein preserved MSP1(19) epitopes recognized by Sera collected from P. vivax infected humans and TLR5 agonist activity. Mice parenterally immunized with recombinant P vivax MSPI 19 in the presence of FliC, either admixed or genetically linked, elicited strong and long-lasting MSP1 (19)-specific systemic antibody responses with a prevailing IgG1 subclass response. Incorporation of another TLR agonist, CpG ODN 1826, resulted in a more balanced response, as evaluated by the IgG1/IgG2c ratio, and higher cell-mediated immune response measured by interferon-gamma secretion. Finally, we show that MSPI 19-specific antibodies recognized the native protein expressed on the surface of P. vivax parasites harvested from infected humans. The present report proposes a new class of malaria vaccine formulation based on the use of malaria antigens and the innate immunity agonist FliC. it contains intrinsic adjuvant properties and enhanced ability to induce specific humoral and cellular immune responses when administered alone or in combination with other adjuvants. (C) 2008 Elsevier Ltd. All rights reserved.

FAPESP Fundacao de Amparo A Pesquisa do Estado de Sao Paulo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo A Pesquisa do Estado do Rio de Janeiro (FAPERJ)

Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)

The Millennium Institute for Vaccine Development and Technology[CNPq-420067/2005-1]

The Millennium Institute for Vaccine Development and Technology

DYB

DYB

DSR

DSR

CJMB

CJMB

BOC

BOC

NME

NME

FAPESR

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FTMC

FTMC

AJV

AJV

LCSF

LCSF

ISS

ISS

MMR

MMR

CNPq

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

VACCINE, v.26, n.48, p.6132-6142, 2008

0264-410X

http://producao.usp.br/handle/BDPI/28347

10.1016/j.vaccine.2008.08.070

http://dx.doi.org/10.1016/j.vaccine.2008.08.070

Idioma(s)

eng

Publicador

ELSEVIER SCI LTD

Relação

Vaccine

Direitos

restrictedAccess

Copyright ELSEVIER SCI LTD

Palavras-Chave #P vivax #Vaccine #Flagellin #FliC #TLR5 #CpG ODN #TLR9 #TRANSMISSION-BLOCKING ACTIVITY #DUFFY-BINDING-PROTEIN #CARBOXYL-TERMINAL FRAGMENT #RECOMBINANT PROTEIN #AOTUS MONKEYS #PROTECTIVE IMMUNITY #ESCHERICHIA-COLI #ANTIBODY TITER #ADJUVANT ACTIVITY #FUSION PROTEINS #Immunology #Medicine, Research & Experimental
Tipo

article

original article

publishedVersion