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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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Published in: | Molecular biotechnology 2024-02, Vol.66 (2), p.222-232 |
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creator | Artarini, Anita Hadianti, Tia Giri-Rachman, Ernawati Arifin Tan, Marselina Irasonia Safitri, Intan A. Hidayat, Nurhamidah A. Retnoningrum, Debbie S. Natalia, Dessy |
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. |
doi_str_mv | 10.1007/s12033-023-00749-4 |
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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.</description><identifier>ISSN: 1073-6085</identifier><identifier>EISSN: 1559-0305</identifier><identifier>DOI: 10.1007/s12033-023-00749-4</identifier><identifier>PMID: 37076664</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adenoviridae - genetics ; Adenovirus ; Adenoviruses ; Animals ; Antibodies, Viral ; Biochemistry ; Biological Techniques ; Biotechnology ; Cell Biology ; Chemistry ; Chemistry and Materials Science ; COVID-19 ; COVID-19 vaccines ; COVID-19 Vaccines - genetics ; Enzyme-linked immunosorbent assay ; Gene expression ; Genomes ; Glycoproteins ; Human Genetics ; Humans ; Immunogenicity ; Immunoglobulin G ; In vivo methods and tests ; Indonesia ; Mice ; Original Paper ; Pandemics ; Pandemics - prevention & control ; Protein Science ; SARS-CoV-2 - genetics ; Severe acute respiratory syndrome coronavirus 2 ; Transgenes ; Vaccines ; Viral diseases ; γ-Interferon</subject><ispartof>Molecular biotechnology, 2024-02, Vol.66 (2), p.222-232</ispartof><rights>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.</rights><rights>2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>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.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c426t-96475d5edfb1e9fa996620a4e9892c041c87c99d7e18dc8cc12de63792f0cbb93</cites><orcidid>0000-0003-0597-4317 ; 0000-0001-8228-1149 ; 0000-0002-0235-7973 ; 0000-0001-9938-8663 ; 0000-0002-1661-9073</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37076664$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Artarini, Anita</creatorcontrib><creatorcontrib>Hadianti, Tia</creatorcontrib><creatorcontrib>Giri-Rachman, Ernawati Arifin</creatorcontrib><creatorcontrib>Tan, Marselina Irasonia</creatorcontrib><creatorcontrib>Safitri, Intan A.</creatorcontrib><creatorcontrib>Hidayat, Nurhamidah A.</creatorcontrib><creatorcontrib>Retnoningrum, Debbie S.</creatorcontrib><creatorcontrib>Natalia, Dessy</creatorcontrib><title>Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia</title><title>Molecular biotechnology</title><addtitle>Mol Biotechnol</addtitle><addtitle>Mol Biotechnol</addtitle><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.</description><subject>Adenoviridae - genetics</subject><subject>Adenovirus</subject><subject>Adenoviruses</subject><subject>Animals</subject><subject>Antibodies, Viral</subject><subject>Biochemistry</subject><subject>Biological Techniques</subject><subject>Biotechnology</subject><subject>Cell Biology</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>COVID-19</subject><subject>COVID-19 vaccines</subject><subject>COVID-19 Vaccines - genetics</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Glycoproteins</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Immunogenicity</subject><subject>Immunoglobulin G</subject><subject>In vivo methods and tests</subject><subject>Indonesia</subject><subject>Mice</subject><subject>Original Paper</subject><subject>Pandemics</subject><subject>Pandemics - prevention & control</subject><subject>Protein Science</subject><subject>SARS-CoV-2 - genetics</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Transgenes</subject><subject>Vaccines</subject><subject>Viral diseases</subject><subject>γ-Interferon</subject><issn>1073-6085</issn><issn>1559-0305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kctuVDEMhiMEohd4ARboSGzYBJz7yQq1QymVKrEBtlEm8SmpziRDMmck3p7AlHJZsLDiyJ9_2_oJecbgFQMwrxvjIAQF3gOMtFQ-IMdMKUtBgHrYczCCahjVETlp7RaAMyXFY3IkDBittTwml29xj3PZbjDvhjINZxFz2ae6NHruG8Zh1X-RMjt89iGkjMPK55ii3-GQ8nCVY8nYkn9CHk1-bvj07j0ln95dfFy9p9cfLq9WZ9c0SK531GppVFQYpzVDO3lrtebgJdrR8gCShdEEa6NBNsYwhsB4RC2M5ROE9dqKU_LmoLtd1huMoa9d_ey2NW18_eaKT-7vSk5f3E3ZOwaMKWF0V3h5p1DL1wXbzm1SCzjPPmNZmuMjCKvFKFRHX_yD3pal5n6f45YZyQHY2Cl-oEItrVWc7rdh4H4Y5Q5GuW6U-2mUk73p-Z933Lf8cqYD4gC0Xso3WH_P_o_sd8HlnXo</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Artarini, Anita</creator><creator>Hadianti, Tia</creator><creator>Giri-Rachman, Ernawati Arifin</creator><creator>Tan, Marselina Irasonia</creator><creator>Safitri, Intan A.</creator><creator>Hidayat, Nurhamidah A.</creator><creator>Retnoningrum, Debbie S.</creator><creator>Natalia, Dessy</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0597-4317</orcidid><orcidid>https://orcid.org/0000-0001-8228-1149</orcidid><orcidid>https://orcid.org/0000-0002-0235-7973</orcidid><orcidid>https://orcid.org/0000-0001-9938-8663</orcidid><orcidid>https://orcid.org/0000-0002-1661-9073</orcidid></search><sort><creationdate>20240201</creationdate><title>Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia</title><author>Artarini, Anita ; 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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.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>37076664</pmid><doi>10.1007/s12033-023-00749-4</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-0597-4317</orcidid><orcidid>https://orcid.org/0000-0001-8228-1149</orcidid><orcidid>https://orcid.org/0000-0002-0235-7973</orcidid><orcidid>https://orcid.org/0000-0001-9938-8663</orcidid><orcidid>https://orcid.org/0000-0002-1661-9073</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenoviridae - genetics Adenovirus Adenoviruses Animals Antibodies, Viral Biochemistry Biological Techniques Biotechnology Cell Biology Chemistry Chemistry and Materials Science COVID-19 COVID-19 vaccines COVID-19 Vaccines - genetics Enzyme-linked immunosorbent assay Gene expression Genomes Glycoproteins Human Genetics Humans Immunogenicity Immunoglobulin G In vivo methods and tests Indonesia Mice Original Paper Pandemics Pandemics - prevention & control Protein Science SARS-CoV-2 - genetics Severe acute respiratory syndrome coronavirus 2 Transgenes Vaccines Viral diseases γ-Interferon |
title | Development of Adenovirus-Based Covid-19 Vaccine Candidate in Indonesia |
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