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A Therapeutic Oral Vaccine Candidate against Propionibacterium acnes: Preparation and Immunological Evaluation of Nanoparticles Encapsulated Sialidase-CAMP Fusion Protein
Parvin, Zargham; Kowsar, Mansouri; Jafar, Amani; Jafar, Salimian; Ali, Ahmadi.
  • Parvin, Zargham; Islamic Azad University. Faculty of Advanced Sciences and Technology. Department of Molecular and Cellular Sciences. Tehran. IR
  • Kowsar, Mansouri; Baqiyatallah University of Medical Sciences. New Hearing Technologies Research Center. Tehran. IR
  • Jafar, Amani; Baqiyatallah University of Medical Sciences. Systems biology and poisonings institute. Molecular Biology Research Center. Tehran. IR
  • Jafar, Salimian; Baqiyatallah University of Medical Sciences. Systems biology and poisonings institute. Chemical Injuries Research Center. Tehran. IR
  • Ali, Ahmadi; Baqiyatallah University of Medical Sciences. Systems biology and poisonings institute. Molecular Biology Research Center. Tehran. IR
Braz. arch. biol. technol ; 63: e20190427, 2020. tab, graf
Article in English | LILACS | ID: biblio-1132174
ABSTRACT
Abstract Acne Vulgaris is a common skin disease caused by Propionibacterium acnes, an anaerobic microbiota of human skin that plays a vital role in the pathology of acne. The aim of this study was to prepare nanoparticles containing an acne recombinant protein and determine its ability as an oral acne vaccine in mice. The recombinant Sialidase-CAMP gene was expressed and purified in a prokaryotic host. The chitosan nanoparticles containing the recombinant protein were prepared, encapsulated, and administered by both oral and subcutaneous routes to Balb/c mice. Sera IgA and IgG and stool IgA titers were measured by ELISA, and the immunized mice were challenged against P. acnes. A 65 kDa recombinant protein was confirmed by SDS-PAGE and western blot. The size and zeta potential of nanoparticles were 80 nm and +18 mV, respectively. After oral immunization, the serum IgG and IgA titers were 13200 and 116, respectively, and the stool IgA titer was 18. In the subcutaneous route, the serum IgG titer was 151200. Immunized mice showed no inflammation in the ear of challenged mice. It is the first study that examines a chitosan-nanoparticulated acne fusion protein as an applicable acne vaccine candidate with appropriate immunogenicity potential. Further studies are required to validate the clinical usefulness of this vaccine candidate.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Propionibacterium acnes / Acne Vulgaris / Chitosan / Nanoparticles Limits: Animals Language: English Journal: Braz. arch. biol. technol Journal subject: Biology Year: 2020 Type: Article Affiliation country: Iran Institution/Affiliation country: Baqiyatallah University of Medical Sciences/IR / Islamic Azad University/IR

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Full text: Available Index: LILACS (Americas) Main subject: Propionibacterium acnes / Acne Vulgaris / Chitosan / Nanoparticles Limits: Animals Language: English Journal: Braz. arch. biol. technol Journal subject: Biology Year: 2020 Type: Article Affiliation country: Iran Institution/Affiliation country: Baqiyatallah University of Medical Sciences/IR / Islamic Azad University/IR