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PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2
The rapid development of safe and effective vaccines against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is a necessary response to coronavirus outbreak. Here, we developed PRAK-03202, the world's first triple antigen virus-like particle vaccine candidate, by cloning and transf...
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/PMC8487870/ https://www.ncbi.nlm.nih.gov/pubmed/34632131 http://dx.doi.org/10.1016/j.heliyon.2021.e08124 |
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author | Mazumder, Saumyabrata Rastogi, Ruchir Undale, Avinash Arora, Kajal Arora, Nupur Mehrotra Pratim, Biswa Kumar, Dilip Joseph, Abyson Mali, Bhupesh Arya, Vidya Bhushan Kalyanaraman, Sriganesh Mukherjee, Abhishek Gupta, Aditi Potdar, Swaroop Roy, Sourav Singha Parashar, Deepak Paliwal, Jeny Singh, Sudhir Kumar Naqvi, Aelia Srivastava, Apoorva Singh, Manglesh Kumar Kumar, Devanand Bansal, Sarthi Rautray, Satabdi Saini, Manish Jain, Kshipra Gupta, Reeshu Kundu, Prabuddha Kumar |
author_facet | Mazumder, Saumyabrata Rastogi, Ruchir Undale, Avinash Arora, Kajal Arora, Nupur Mehrotra Pratim, Biswa Kumar, Dilip Joseph, Abyson Mali, Bhupesh Arya, Vidya Bhushan Kalyanaraman, Sriganesh Mukherjee, Abhishek Gupta, Aditi Potdar, Swaroop Roy, Sourav Singha Parashar, Deepak Paliwal, Jeny Singh, Sudhir Kumar Naqvi, Aelia Srivastava, Apoorva Singh, Manglesh Kumar Kumar, Devanand Bansal, Sarthi Rautray, Satabdi Saini, Manish Jain, Kshipra Gupta, Reeshu Kundu, Prabuddha Kumar |
author_sort | Mazumder, Saumyabrata |
collection | PubMed |
description | The rapid development of safe and effective vaccines against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is a necessary response to coronavirus outbreak. Here, we developed PRAK-03202, the world's first triple antigen virus-like particle vaccine candidate, by cloning and transforming SARS-CoV-2 gene segments into a highly characterized S. cerevisiae-based D-Crypt™ platform, which induced SARS CoV-2 specific neutralizing antibodies in BALB/c mice. Immunization using three different doses of PRAK-03202 induced an antigen-specific (spike, envelope, and membrane proteins) humoral response and neutralizing potential. Peripheral blood mononuclear cells from convalescent patients showed lymphocyte proliferation and elevated interferon levels suggestive of epitope conservation and induction of T helper 1-biased cellular immune response when exposed to PRAK-03202. These data support further clinical development and testing of PRAK-03202 for use in humans. |
format | Online Article Text |
id | pubmed-8487870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-84878702021-10-04 PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2 Mazumder, Saumyabrata Rastogi, Ruchir Undale, Avinash Arora, Kajal Arora, Nupur Mehrotra Pratim, Biswa Kumar, Dilip Joseph, Abyson Mali, Bhupesh Arya, Vidya Bhushan Kalyanaraman, Sriganesh Mukherjee, Abhishek Gupta, Aditi Potdar, Swaroop Roy, Sourav Singha Parashar, Deepak Paliwal, Jeny Singh, Sudhir Kumar Naqvi, Aelia Srivastava, Apoorva Singh, Manglesh Kumar Kumar, Devanand Bansal, Sarthi Rautray, Satabdi Saini, Manish Jain, Kshipra Gupta, Reeshu Kundu, Prabuddha Kumar Heliyon Research Article The rapid development of safe and effective vaccines against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is a necessary response to coronavirus outbreak. Here, we developed PRAK-03202, the world's first triple antigen virus-like particle vaccine candidate, by cloning and transforming SARS-CoV-2 gene segments into a highly characterized S. cerevisiae-based D-Crypt™ platform, which induced SARS CoV-2 specific neutralizing antibodies in BALB/c mice. Immunization using three different doses of PRAK-03202 induced an antigen-specific (spike, envelope, and membrane proteins) humoral response and neutralizing potential. Peripheral blood mononuclear cells from convalescent patients showed lymphocyte proliferation and elevated interferon levels suggestive of epitope conservation and induction of T helper 1-biased cellular immune response when exposed to PRAK-03202. These data support further clinical development and testing of PRAK-03202 for use in humans. Elsevier 2021-10-04 /pmc/articles/PMC8487870/ /pubmed/34632131 http://dx.doi.org/10.1016/j.heliyon.2021.e08124 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Mazumder, Saumyabrata Rastogi, Ruchir Undale, Avinash Arora, Kajal Arora, Nupur Mehrotra Pratim, Biswa Kumar, Dilip Joseph, Abyson Mali, Bhupesh Arya, Vidya Bhushan Kalyanaraman, Sriganesh Mukherjee, Abhishek Gupta, Aditi Potdar, Swaroop Roy, Sourav Singha Parashar, Deepak Paliwal, Jeny Singh, Sudhir Kumar Naqvi, Aelia Srivastava, Apoorva Singh, Manglesh Kumar Kumar, Devanand Bansal, Sarthi Rautray, Satabdi Saini, Manish Jain, Kshipra Gupta, Reeshu Kundu, Prabuddha Kumar PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2 |
title | PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2 |
title_full | PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2 |
title_fullStr | PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2 |
title_full_unstemmed | PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2 |
title_short | PRAK-03202: A triple antigen virus-like particle vaccine candidate against SARS CoV-2 |
title_sort | prak-03202: a triple antigen virus-like particle vaccine candidate against sars cov-2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487870/ https://www.ncbi.nlm.nih.gov/pubmed/34632131 http://dx.doi.org/10.1016/j.heliyon.2021.e08124 |
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