Surface Immunogenic Protein of Streptococcus Group B is an Agonist of Toll-Like Receptors 2 and 4 and a Potential Immune Adjuvant

被引:7
作者
Diaz-Dinamarca, Diego A. [1 ,2 ]
Manzo, Ricardo A. [1 ]
Soto, Daniel A. [1 ]
Jose Avendano-Valenzuela, Maria [1 ,2 ]
Bastias, Diego N. [1 ,2 ,3 ]
Soto, Paulina, I [1 ]
Escobar, Daniel F. [1 ]
Vasquez-Saez, Valeria [1 ]
Carrion, Flavio [4 ]
Pizarro-Ortega, Magdalena S. [2 ]
Wilson, Christian A. M. [5 ]
Berrios, Julio [6 ]
Kalergis, Alexis M. [2 ,7 ]
Vasquez, Abel E. [1 ,3 ,8 ]
机构
[1] Inst Salud Publ Chile, Secc Biotecnol, Santiago 7780050, Chile
[2] Pontificia Univ Catolica Chile, Fac Ciencias Biol, Millenium Inst Immunol & Immunotherapy, Dept Genet Mol & Microbiol, Santiago 8320000, Chile
[3] Univ Santo Tomas, Fac Ciencias, Escuela Biotecnol, Santiago 8320000, Chile
[4] Clin Alemana Univ Desarrollo, Fac Med, Programa Inmunol Traslac, Santiago 8320000, Chile
[5] Univ Chile, Fac Ciencias Quim & Farmaceut, Dept Bioquim & Biol Mol, Santiago 8320000, Chile
[6] Pontificia Univ Catolica Valparaiso, Escuela Ingn Bioquim, Valparaiso 2340000, Chile
[7] Pontificia Univ Catolica Chile, Fac Med, Dept Endocrinol, Santiago 8320000, Chile
[8] Univ San Sebastian, Fac Ciencia, Santiago 8320000, Chile
关键词
surface immunogenic protein; group B Streptococcus; TRL2 and TLR4 agonist; adjuvant protein; DENDRITIC CELLS; RESPONSES; TLR2; PROMOTES; KINASE; TH1;
D O I
10.3390/vaccines8010029
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:13
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