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Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation
We report the development and evaluation of safety and immunogenicity of a whole virion inactivated (WVI) SARS-CoV-2 vaccine (BBV152), adjuvanted with aluminum hydroxide gel (Algel), or TLR7/8 agonist chemisorbed Algel. We used a well-characterized SARS-CoV-2 strain and an established Vero cell plat...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944858/ https://www.ncbi.nlm.nih.gov/pubmed/33723528 http://dx.doi.org/10.1016/j.isci.2021.102298 |
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author | Ganneru, Brunda Jogdand, Harsh Daram, Vijaya Kumar Das, Dipankar Molugu, Narasimha Reddy Prasad, Sai D. Kannappa, Srinivas V. Ella, Krishna M. Ravikrishnan, Rajaram Awasthi, Amit Jose, Jomy Rao, Panduranga Kumar, Deepak Ella, Raches Abraham, Priya Yadav, Pragya D. Sapkal, Gajanan N. Shete-Aich, Anita Desphande, Gururaj Mohandas, Sreelekshmy Basu, Atanu Gupta, Nivedita Vadrevu, Krishna Mohan |
author_facet | Ganneru, Brunda Jogdand, Harsh Daram, Vijaya Kumar Das, Dipankar Molugu, Narasimha Reddy Prasad, Sai D. Kannappa, Srinivas V. Ella, Krishna M. Ravikrishnan, Rajaram Awasthi, Amit Jose, Jomy Rao, Panduranga Kumar, Deepak Ella, Raches Abraham, Priya Yadav, Pragya D. Sapkal, Gajanan N. Shete-Aich, Anita Desphande, Gururaj Mohandas, Sreelekshmy Basu, Atanu Gupta, Nivedita Vadrevu, Krishna Mohan |
author_sort | Ganneru, Brunda |
collection | PubMed |
description | We report the development and evaluation of safety and immunogenicity of a whole virion inactivated (WVI) SARS-CoV-2 vaccine (BBV152), adjuvanted with aluminum hydroxide gel (Algel), or TLR7/8 agonist chemisorbed Algel. We used a well-characterized SARS-CoV-2 strain and an established Vero cell platform to produce large-scale GMP-grade highly purified inactivated antigen. Product development and manufacturing process were carried out in a BSL-3 facility. Immunogenicity and safety were determined at two antigen concentrations (3μg and 6μg), with two different adjuvants, in mice, rats, and rabbits. Our results show that BBV152 vaccine formulations generated significantly high antigen-binding and neutralizing antibody titers (NAb), at both concentrations, in all three species with excellent safety profiles. The inactivated vaccine formulation contains TLR7/8 agonist adjuvant-induced Th1-biased antibody responses with elevated IgG2a/IgG1 ratio and increased levels of SARS-CoV-2-specific IFN-γ(+) CD4(+) T lymphocyte response. Our results support further development for phase I/II clinical trials in humans. |
format | Online Article Text |
id | pubmed-7944858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79448582021-03-11 Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation Ganneru, Brunda Jogdand, Harsh Daram, Vijaya Kumar Das, Dipankar Molugu, Narasimha Reddy Prasad, Sai D. Kannappa, Srinivas V. Ella, Krishna M. Ravikrishnan, Rajaram Awasthi, Amit Jose, Jomy Rao, Panduranga Kumar, Deepak Ella, Raches Abraham, Priya Yadav, Pragya D. Sapkal, Gajanan N. Shete-Aich, Anita Desphande, Gururaj Mohandas, Sreelekshmy Basu, Atanu Gupta, Nivedita Vadrevu, Krishna Mohan iScience Article We report the development and evaluation of safety and immunogenicity of a whole virion inactivated (WVI) SARS-CoV-2 vaccine (BBV152), adjuvanted with aluminum hydroxide gel (Algel), or TLR7/8 agonist chemisorbed Algel. We used a well-characterized SARS-CoV-2 strain and an established Vero cell platform to produce large-scale GMP-grade highly purified inactivated antigen. Product development and manufacturing process were carried out in a BSL-3 facility. Immunogenicity and safety were determined at two antigen concentrations (3μg and 6μg), with two different adjuvants, in mice, rats, and rabbits. Our results show that BBV152 vaccine formulations generated significantly high antigen-binding and neutralizing antibody titers (NAb), at both concentrations, in all three species with excellent safety profiles. The inactivated vaccine formulation contains TLR7/8 agonist adjuvant-induced Th1-biased antibody responses with elevated IgG2a/IgG1 ratio and increased levels of SARS-CoV-2-specific IFN-γ(+) CD4(+) T lymphocyte response. Our results support further development for phase I/II clinical trials in humans. Elsevier 2021-03-10 /pmc/articles/PMC7944858/ /pubmed/33723528 http://dx.doi.org/10.1016/j.isci.2021.102298 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ganneru, Brunda Jogdand, Harsh Daram, Vijaya Kumar Das, Dipankar Molugu, Narasimha Reddy Prasad, Sai D. Kannappa, Srinivas V. Ella, Krishna M. Ravikrishnan, Rajaram Awasthi, Amit Jose, Jomy Rao, Panduranga Kumar, Deepak Ella, Raches Abraham, Priya Yadav, Pragya D. Sapkal, Gajanan N. Shete-Aich, Anita Desphande, Gururaj Mohandas, Sreelekshmy Basu, Atanu Gupta, Nivedita Vadrevu, Krishna Mohan Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation |
title | Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation |
title_full | Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation |
title_fullStr | Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation |
title_full_unstemmed | Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation |
title_short | Th1 skewed immune response of whole virion inactivated SARS CoV 2 vaccine and its safety evaluation |
title_sort | th1 skewed immune response of whole virion inactivated sars cov 2 vaccine and its safety evaluation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944858/ https://www.ncbi.nlm.nih.gov/pubmed/33723528 http://dx.doi.org/10.1016/j.isci.2021.102298 |
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