Publications

Detailed Information

A Synthetic Tul4 and FopA Peptide Cocktail of Francisella tularensis Induces Humoral and Cell-Mediated Immune Responses in Mice

DC Field Value Language
dc.contributor.authorOh, Hanseul-
dc.contributor.authorKim, C-Yoon-
dc.contributor.authorKim, Chang-Hwan-
dc.contributor.authorHur, Gyeung-Haeng-
dc.contributor.authorPark, Jae-Hak-
dc.date.accessioned2023-07-07T07:59:17Z-
dc.date.available2023-07-07T07:59:17Z-
dc.date.created2018-09-10-
dc.date.created2018-09-10-
dc.date.issued2016-09-
dc.identifier.citationJournal of Microbiology and Biotechnology, Vol.26 No.9, pp.1613-1619-
dc.identifier.issn1017-7825-
dc.identifier.urihttps://hdl.handle.net/10371/194771-
dc.description.abstractFrancisella tularensis is a highly virulent pathogen of humans and other mammals. Moreover, F. tularensis has been designated a category A biothreat agent, and there is growing interest in the development of a protective vaccine. In the present study, we determine the in vitro and in vivo immune responses of a subunit vaccine composed of recombinant peptides Tul4 and FopA from epitopes of the F. tularensis outer membrane proteins. The recombinant peptides with adjuvant CpG induced robust immunophenotypic change of dendritic cell (DC) maturation and secretion of inflammatory cytokines (IL-6, IL-12). In addition, the matured DCs enabled ex vivo proliferation of naive splenocytes in a mixed lymphocyte reaction. Lastly, we determined the in vivo immune response by assessment of antibody production in C57BL/6 mice. Total IgG levels were produced after immunization and peaked in 6 weeks, and moreover, Tul4-specific IgG was confirmed in the mice receiving peptides with or without CpG. Based on these results, we concluded that the recombinant peptides Tul4 and FopA have immunogenicity and could be a safe subunit vaccine candidate approach against F. tularensis.-
dc.language영어-
dc.publisher한국미생물·생명공학회-
dc.titleA Synthetic Tul4 and FopA Peptide Cocktail of Francisella tularensis Induces Humoral and Cell-Mediated Immune Responses in Mice-
dc.typeArticle-
dc.identifier.doi10.4014/jmb.1602.02022-
dc.citation.journaltitleJournal of Microbiology and Biotechnology-
dc.identifier.wosid000385018300014-
dc.identifier.scopusid2-s2.0-84989163855-
dc.citation.endpage1619-
dc.citation.number9-
dc.citation.startpage1613-
dc.citation.volume26-
dc.identifier.kciidART002147197-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorPark, Jae-Hak-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusDENDRITIC CELLS-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusTULAREMIA-
dc.subject.keywordPlusIL-6-
dc.subject.keywordAuthorFrancisella tularensis-
dc.subject.keywordAuthorTul4-
dc.subject.keywordAuthorFopA-
dc.subject.keywordAuthorsubunit vaccine-
dc.subject.keywordAuthorimmune response-
Appears in Collections:
Files in This Item:
There are no files associated with this item.

Related Researcher

  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Laboratory Animal Medicine, Toxicologic Pathology

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share