New malaria vaccine candidates based on the Plasmodium vivax Merozoite Surface Protein-1 and the TLR-5 agonist Salmonella Typhimurium FliC flagellin
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2008
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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 |
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 |