Surface Immunogenic Protein of Streptococcus Group B is an Agonist of Toll-Like Receptors 2 and 4 and a Potential Immune Adjuvant
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2020Metadata
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Díaz Dinamarca, Diego A.
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Surface Immunogenic Protein of Streptococcus Group B is an Agonist of Toll-Like Receptors 2 and 4 and a Potential Immune Adjuvant
Author
- Díaz Dinamarca, Diego A.;
- Manzo, Ricardo A.;
- Soto, Daniel A.;
- Avendaño Valenzuela, María José;
- Bastías, Diego N.;
- Soto, Paulina I.;
- Escobar, Daniel F.;
- Vásquez Sáez, Valeria;
- Carrión, Flavio;
- Pizarro Ortega, Magdalena S.;
- Wilson Moya, Christian A. M.;
- Berríos, Julio;
- Kalergis, Alexis M.;
- Vásquez, Abel E.;
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)-gamma, Tumor Necrosis Factor (TNF)-alpha, 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-gamma. 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.
Patrocinador
FONDEF D10i1202
Millennium Institute on Immunology and Immunotherapy P09/016-F
Instituto de Salud Publica de Chile (Institute of Public Health in Santiago, Chile)
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Artículo de publicación ISI Artículo de publicación SCOPUS
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Vaccines (2020), 8(1), 29
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