Cargando…
Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models
Development 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...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789841/ https://www.ncbi.nlm.nih.gov/pubmed/31527460 http://dx.doi.org/10.3390/vaccines7030115 |
_version_ | 1783458705731223552 |
---|---|
author | Aligholipour Farzani, Touraj Földes, Katalin Ergünay, Koray Gurdal, Hakan Bastug, Aliye Ozkul, Aykut |
author_facet | Aligholipour Farzani, Touraj Földes, Katalin Ergünay, Koray Gurdal, Hakan Bastug, Aliye Ozkul, Aykut |
author_sort | Aligholipour Farzani, Touraj |
collection | PubMed |
description | Development 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. |
format | Online Article Text |
id | pubmed-6789841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67898412019-10-16 Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models Aligholipour Farzani, Touraj Földes, Katalin Ergünay, Koray Gurdal, Hakan Bastug, Aliye Ozkul, Aykut Vaccines (Basel) Article Development 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. MDPI 2019-09-16 /pmc/articles/PMC6789841/ /pubmed/31527460 http://dx.doi.org/10.3390/vaccines7030115 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Aligholipour Farzani, Touraj Földes, Katalin Ergünay, Koray Gurdal, Hakan Bastug, Aliye Ozkul, Aykut Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models |
title | Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models |
title_full | Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models |
title_fullStr | Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models |
title_full_unstemmed | Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models |
title_short | Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models |
title_sort | immunological analysis of a cchfv mrna vaccine candidate in mouse models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789841/ https://www.ncbi.nlm.nih.gov/pubmed/31527460 http://dx.doi.org/10.3390/vaccines7030115 |
work_keys_str_mv | AT aligholipourfarzanitouraj immunologicalanalysisofacchfvmrnavaccinecandidateinmousemodels AT foldeskatalin immunologicalanalysisofacchfvmrnavaccinecandidateinmousemodels AT ergunaykoray immunologicalanalysisofacchfvmrnavaccinecandidateinmousemodels AT gurdalhakan immunologicalanalysisofacchfvmrnavaccinecandidateinmousemodels AT bastugaliye immunologicalanalysisofacchfvmrnavaccinecandidateinmousemodels AT ozkulaykut immunologicalanalysisofacchfvmrnavaccinecandidateinmousemodels |