Surface Immunogenic Protein of Streptococcus Group B is an Agonist of Toll-Like Receptors 2 and 4 and a Potential Immune Adjuvant
Authors:
- Diego A. Diaz-DinamarcaDiego A. Diaz-Dinamarca
- Ricardo A. ManzoRMRicardo A. Manzo
- Daniel A. SotoDSDaniel A. Soto
- María José Avendaño-ValenzuelaMAMaría José Avendaño-Valenzuela
- Diego N. BastiasDBDiego N. Bastias
- Paulina I. SotoPSPaulina I. Soto
- Daniel F. EscobarDEDaniel F. Escobar
- Valeria Vasquez-SaezVVValeria Vasquez-Saez
- Flavio CarriónFCFlavio Carrión
- Magdalena S. Pizarro-OrtegaMPMagdalena S. Pizarro-Ortega
- Christian A. M. WilsonCWChristian A. M. Wilson
- Julio BerriosJulio Berrios
Open Access
Abstract
Vaccine-induced protection against pathogens, especially subunit-based vaccines, are related to antigen properties but mainly in their ability to stimulate the immune system by the use of an adjuvant. Modern vaccines are formulated with a high level of antigen purity, where an efficient adjuvant is necessary. In this context, the use of protein Toll-Like Receptor (TLR) agonists as vaccine adjuvants has been highlighted because of their optimal immunogenicity and minimal toxicity. The Surface Immunogenic Protein (SIP) from Group B Streptococcus (GBS) has gained importance as a new potential protein-based vaccine. Recently, we reported that recombinant SIP (rSIP) expressed by E. coli and purified by High Performance Liquid Chromatography (HPLC) alone induces a protective humoral immune response. In this study, we present the immunomodulatory properties of rSIP as a protein-based adjuvant, as an agonist of TLR. To this end, we showed that C57BL/6 bone marrow-derived dendritic cells pulsed by rSIP resulted in enhanced CD40, CD80, CD86, and Major Histocompatibility Complex (MHC) class II as well as increased secretion proinflammatory cytokines Interleukin (IL)-6, Interferon (IFN)-γ, Tumor Necrosis Factor (TNF)-α, and IL-10. Next, we investigated the in vivo effect of rSIP in the absence or presence of ovalbumin (OVA) on antigen-specific antibody secretion in C57BL/6 mice. Immunization with rSIP plus OVA showed that anti-OVA IgG2a and IgG1a increased significantly compared with OVA alone in C57BL/6 mice. Also, the immunization of rSIP plus OVA generates increased serum cytokines levels characterized by IL-12p70, IL-10, IL-4, and IFN-γ. Interestingly, we observed that rSIP stimulate Toll Like Receptor (TLR)2 and TLR4, individually expressed by Human embryonic kidney (HEK) 293-derived TLR reporter cells. These findings suggest that rSIP is a new potential protein TLR agonist adjuvant and may be employed in the development of new vaccines.Keywords
This publication has 35 references indexed in Scilit:
- Immunostimulation by Synthetic Lipopeptide-Based Vaccine Candidates: Structure-Activity RelationshipsFrontiers in Immunology, 2013
- Synthetic Toll Like Receptor-4 (TLR-4) Agonist Peptides as a Novel Class of AdjuvantsPLOS ONE, 2012
- Toll-like Receptors and Their Crosstalk with Other Innate Receptors in Infection and ImmunityImmunity, 2011
- Programmed cell death of dendritic cells in immune regulationImmunological Reviews, 2010
- 34kDa MOMP of Shigella flexneri promotes TLR2 mediated macrophage activation with the engagement of NF-κB and p38 MAP kinase signalingMolecular Immunology, 2010
- The PorB porin from commensal Neisseria lactamica induces Th1 and Th2 immune responses to ovalbumin in mice and is a potential immune adjuvantVaccine, 2008
- The adaptor molecule TIRAP provides signalling specificity for Toll-like receptorsNature, 2002
- Adjuvants of ImmunityJournal of Experimental Medicine, 2002
- Toll-like Receptor 2 (TLR2) and TLR4 Differentially Activate Human Dendritic CellsJournal of Biological Chemistry, 2001
- TH1 and TH2 Cells: Different Patterns of Lymphokine Secretion Lead to Different Functional PropertiesAnnual Review of Immunology, 1989