Repository of Research and Investigative Information

Repository of Research and Investigative Information

Baqiyatallah University of Medical Sciences

EspA-loaded mesoporous silica nanoparticles can efficiently protect animal model against enterohaemorrhagic E-coli O157: H7

(2018) EspA-loaded mesoporous silica nanoparticles can efficiently protect animal model against enterohaemorrhagic E-coli O157: H7. Artificial Cells Nanomedicine and Biotechnology. S1067-S1075. ISSN 2169-1401

[img] Text
EspA-loaded mesoporous silica nanoparticles can efficiently protect animal model against enterohaemorrhagic E. coli O157H7.pdf

Download (2MB)

Official URL: http://apps.webofknowledge.com/InboundService.do?F...

Abstract

In the present study, the application of mesoporous silica nanoparticles (MSNPs) loaded with recombinant EspA protein, an immunogen of enterohaemorrhagic E. coli, was investigated in the case of BALB/c mice immunization against the bacterium. MSNPs of 96.9 +/- 15.9 nm in diameter were synthesized using template removing method. The immunization of mice was carried out orally and subcutaneously. Significant immune responses to the antigen were observed for the immunized mice when rEspA-loaded MSNPs were administered in both routes in comparison to that of the antigen formulated using a well-known adjuvant, i.e. Freund's. According to the titretitre of serum IL-4, the most potent humoral responses were observed when the mice were immunized subcutaneously with antigen-loaded MSNPs (244, 36 and 14 ng/dL of IL-4 in the serum of mice immunized subcutaneously or orally by antigen-loaded MSNPs, and subcutaneously by Freund's adjuvant formulated-antigen, respectively). However, the difference in serum IgG and serum IgA was not significant in mice subcutaneously immunized with antigen-loaded MSNPs and mice immunized with Freund's adjuvant formulated-antigen. Finally, the immunized mice were challenged orally by enterohaemorrhagic E. coli cells. The amount of bacterial shedding was significantly reduced in faecesfaeces of the animals immunized by antigen-loaded MSNPs in both subcutaneous and oral routes.

Item Type: Article
Keywords: Mesoporous silica nanoparticles p vaccine delivery enterohaemorrhagic E. coli recombinant vaccine drug-delivery b-cell vaccine responses antigen size membrane adjuvant design mice Biotechnology & Applied Microbiology Engineering Materials Science
Divisions:
Page Range: S1067-S1075
Journal or Publication Title: Artificial Cells Nanomedicine and Biotechnology
Journal Index: ISI
Volume: 46
Identification Number: https://doi.org/10.1080/21691401.2018.1529676
ISSN: 2169-1401
Depositing User: مهندس مهدی شریفی
URI: http://eprints.bmsu.ac.ir/id/eprint/3922

Actions (login required)

View Item View Item