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dc.contributor.authorAligholipour Farzani, Touraj
dc.contributor.authorFöldes, Katalin
dc.contributor.authorErgünay, Koray
dc.contributor.authorGurdal, Hakan
dc.contributor.authorBastug, Aliye
dc.contributor.authorOzkul, Aykut
dc.date.accessioned2021-06-03T06:03:34Z
dc.date.available2021-06-03T06:03:34Z
dc.date.issued2019
dc.identifier.issn2076-393X
dc.identifier.urihttp://dx.doi.org/10.3390/vaccines7030115
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789841/
dc.identifier.urihttp://hdl.handle.net/11655/24199
dc.description.abstractDevelopment of new vaccine platforms against viral diseases is considered urgent. In recent years, mRNA constructs have attracted great interest in this field due to unique advantages over conventional gene transfer platforms. In the present study, we developed a new naked conventional mRNA vaccine expressing the non-optimized small (S) segment of the Ank-2 strain of Crimean-Congo Hemorrhagic Fever virus (CCHFV). We then analyzed its single and booster dose immunogenicity and protection potential in the challenge assay in two mice models, including IFNα/β/γR−/− and C57BL/6. The results obtained from the immunological assays, namely IL-4 and IFN-gamma ELISPOT, intracellular IFN-gamma staining, in-house sandwich ELISA, and survival data, demonstrated that our construct elicited the production of anti-nucleocapsid (N) specific immune responses in both mice models. A 100% protection rate was only obtained in the booster dose group of IFNα/β/γR−/− mice, indicating that this platform needs further optimization in future studies. In conclusion, we assessed a novel approach in CCHFV vaccination by introducing a conventional mRNA platform which can be considered in future experiments as an efficient and safe way to battle this disease.
dc.language.isoen
dc.relation.isversionof10.3390/vaccines7030115
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleImmunological Analysis Of A Cchfv Mrna Vaccine Candidate In Mouse Models
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalVaccines
dc.contributor.departmentTıbbi Mikrobiyoloji
dc.identifier.volume7
dc.identifier.issue3
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus


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Attribution 4.0 United States
Except where otherwise noted, this item's license is described as Attribution 4.0 United States