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Authordc.contributor.authorDíaz Dinamarca, Diego A. 
Authordc.contributor.authorManzo, Ricardo A. 
Authordc.contributor.authorSoto, Daniel A. 
Authordc.contributor.authorAvendaño Valenzuela, María José 
Authordc.contributor.authorBastías, Diego N. 
Authordc.contributor.authorSoto, Paulina I. 
Authordc.contributor.authorEscobar, Daniel F. 
Authordc.contributor.authorVásquez Sáez, Valeria 
Authordc.contributor.authorCarrión, Flavio 
Authordc.contributor.authorPizarro Ortega, Magdalena S. 
Authordc.contributor.authorWilson Moya, Christian A. M. 
Authordc.contributor.authorBerríos, Julio 
Authordc.contributor.authorKalergis, Alexis M. 
Authordc.contributor.authorVásquez, Abel E. 
Admission datedc.date.accessioned2020-06-04T21:44:08Z
Available datedc.date.available2020-06-04T21:44:08Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationVaccines (2020), 8(1), 29es_ES
Identifierdc.identifier.other10.3390/vaccines8010029
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/175262
Abstractdc.description.abstractVaccine-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.es_ES
Patrocinadordc.description.sponsorshipFONDEF D10i1202 Millennium Institute on Immunology and Immunotherapy P09/016-F Instituto de Salud Publica de Chile (Institute of Public Health in Santiago, Chile)es_ES
Publisherdc.publisherMDPIes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceVaccineses_ES
Keywordsdc.subjectSurface immunogenic proteines_ES
Keywordsdc.subjectGroup B Streptococcuses_ES
Keywordsdc.subjectTRL2 and TLR4 agonistes_ES
Keywordsdc.subjectAdjuvant proteines_ES
Títulodc.titleSurface Immunogenic Protein of Streptococcus Group B is an Agonist of Toll-Like Receptors 2 and 4 and a Potential Immune Adjuvantes_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorctces_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile