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Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia

Covid-19 pandemic has struck worldwide by end of 2019 and the use of various vaccine platforms was one of the main strategies to end this. To meet the needs for vaccine technology equality among many countries, we developed adenovirus-based Covid-19 vaccine candidate in Indonesia. SARS-CoV-2 Spike g...

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Autores principales: Artarini, Anita, Hadianti, Tia, Giri-Rachman, Ernawati Arifin, Tan, Marselina Irasonia, Safitri, Intan A., Hidayat, Nurhamidah A., Retnoningrum, Debbie S., Natalia, Dessy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115376/
https://www.ncbi.nlm.nih.gov/pubmed/37076664
http://dx.doi.org/10.1007/s12033-023-00749-4
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author Artarini, Anita
Hadianti, Tia
Giri-Rachman, Ernawati Arifin
Tan, Marselina Irasonia
Safitri, Intan A.
Hidayat, Nurhamidah A.
Retnoningrum, Debbie S.
Natalia, Dessy
author_facet Artarini, Anita
Hadianti, Tia
Giri-Rachman, Ernawati Arifin
Tan, Marselina Irasonia
Safitri, Intan A.
Hidayat, Nurhamidah A.
Retnoningrum, Debbie S.
Natalia, Dessy
author_sort Artarini, Anita
collection PubMed
description Covid-19 pandemic has struck worldwide by end of 2019 and the use of various vaccine platforms was one of the main strategies to end this. To meet the needs for vaccine technology equality among many countries, we developed adenovirus-based Covid-19 vaccine candidate in Indonesia. SARS-CoV-2 Spike gene (S) was constructed into pAdEasy vector. The recombinant serotype 5 Adenovirus (AdV_S) genome was transfected into AD293 cells to produce recombinant adenovirus. Characterization using PCR confirmed the presence of spike gene. Transgene expression analysis showed the expression of S protein in AdV_S infected AD293 and A549 cells. Optimization of viral production showed the highest titer was obtained at MOI of 0.1 and 1 at 4 days. The in vivo study was performed by injecting Balb/c mice with 3.5 × 10(7) ifu of purified adenovirus. The result showed that S1-specific IgG was increased up to 56 days after single-dose administration of AdV_S. Interestingly, significant increase of S1 glycoprotein-specific IFN-γ ELISpot was observed in AdV_S treated Balb/c mice. In conclusion, the AdV_S vaccine candidate was successfully produced at laboratory scale, immunogenic, and did not cause severe inflammation in Balb/c mice. This study serves as initial step towards manufacturing of adenovirus-based vaccine in Indonesia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12033-023-00749-4.
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spelling pubmed-101153762023-04-20 Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia Artarini, Anita Hadianti, Tia Giri-Rachman, Ernawati Arifin Tan, Marselina Irasonia Safitri, Intan A. Hidayat, Nurhamidah A. Retnoningrum, Debbie S. Natalia, Dessy Mol Biotechnol Original Paper Covid-19 pandemic has struck worldwide by end of 2019 and the use of various vaccine platforms was one of the main strategies to end this. To meet the needs for vaccine technology equality among many countries, we developed adenovirus-based Covid-19 vaccine candidate in Indonesia. SARS-CoV-2 Spike gene (S) was constructed into pAdEasy vector. The recombinant serotype 5 Adenovirus (AdV_S) genome was transfected into AD293 cells to produce recombinant adenovirus. Characterization using PCR confirmed the presence of spike gene. Transgene expression analysis showed the expression of S protein in AdV_S infected AD293 and A549 cells. Optimization of viral production showed the highest titer was obtained at MOI of 0.1 and 1 at 4 days. The in vivo study was performed by injecting Balb/c mice with 3.5 × 10(7) ifu of purified adenovirus. The result showed that S1-specific IgG was increased up to 56 days after single-dose administration of AdV_S. Interestingly, significant increase of S1 glycoprotein-specific IFN-γ ELISpot was observed in AdV_S treated Balb/c mice. In conclusion, the AdV_S vaccine candidate was successfully produced at laboratory scale, immunogenic, and did not cause severe inflammation in Balb/c mice. This study serves as initial step towards manufacturing of adenovirus-based vaccine in Indonesia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12033-023-00749-4. Springer US 2023-04-19 /pmc/articles/PMC10115376/ /pubmed/37076664 http://dx.doi.org/10.1007/s12033-023-00749-4 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Paper
Artarini, Anita
Hadianti, Tia
Giri-Rachman, Ernawati Arifin
Tan, Marselina Irasonia
Safitri, Intan A.
Hidayat, Nurhamidah A.
Retnoningrum, Debbie S.
Natalia, Dessy
Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia
title Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia
title_full Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia
title_fullStr Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia
title_full_unstemmed Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia
title_short Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia
title_sort development of adenovirus-based covid-19 vaccine candidate in indonesia
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115376/
https://www.ncbi.nlm.nih.gov/pubmed/37076664
http://dx.doi.org/10.1007/s12033-023-00749-4
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