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PRAK-03202: A triple antigen VLP vaccine candidate against SARS CoV-2
Abstract The rapid development of safe and effective vaccines against SARS CoV-2 is the need of the hour for the coronavirus outbreak. Here, we have developed PRAK-03202, the world’s first triple antigen VLP vaccine candidate in a highly characterized S. cerevisiae-based D-CryptTM platform, which in...
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creator | Mazumder, Saumyabrata Rastogi, Ruchir Undale, Avinash Arora, Kajal Nupur Mehrotra Arora Pratim, Biswa Kumar, Dilip Abyson, Joseph Mali, Bhupesh Arya, Vidya Bhushan Kalyanaraman, Sriganesh Mukherjee, Abhishek Gupta, Aditi Potdar, Swaroop Sourav Singha Roy Parashar, Deepak Paliwal, Jeny Singh, Sudhir Kumar Naqvi, Aelia Srivastava, Apoorva Singh, Manglesh Kumar Kumar, Devanand Bansal, Sarthi Rautray, Satabdi Singh, Indrajeet Fengade, Pankaj Kumar, Bibekanand Saini, Manish Jain, Kshipra Gupta, Reeshu Kundu, Prabuddha Kumar |
description | Abstract The rapid development of safe and effective vaccines against SARS CoV-2 is the need of the hour for the coronavirus outbreak. Here, we have developed PRAK-03202, the world’s first triple antigen VLP vaccine candidate in a highly characterized S. cerevisiae-based D-CryptTM platform, which induced SARS CoV-2 specific neutralizing antibodies in BALB/c mice. Immunizations using three different doses of PRAK-03202 induces antigen specific (Spike, envelope and membrane proteins) humoral response and neutralizing potential. PBMCs from convalescent patients, when exposed to PRAK-03202, showed lymphocyte proliferation and elevated IFN-γ levels suggestive of conservation of epitopes and induction of T helper 1 (Th1)–biased cellular immune responses. These data support the clinical development and testing of PRAK-03202 for use in humans. Competing Interest Statement The authors have declared no competing interest. |
doi_str_mv | 10.1101/2020.10.30.360115 |
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Here, we have developed PRAK-03202, the world’s first triple antigen VLP vaccine candidate in a highly characterized S. cerevisiae-based D-CryptTM platform, which induced SARS CoV-2 specific neutralizing antibodies in BALB/c mice. Immunizations using three different doses of PRAK-03202 induces antigen specific (Spike, envelope and membrane proteins) humoral response and neutralizing potential. PBMCs from convalescent patients, when exposed to PRAK-03202, showed lymphocyte proliferation and elevated IFN-γ levels suggestive of conservation of epitopes and induction of T helper 1 (Th1)–biased cellular immune responses. These data support the clinical development and testing of PRAK-03202 for use in humans. Competing Interest Statement The authors have declared no competing interest.</description><edition>1.1</edition><identifier>EISSN: 2692-8205</identifier><identifier>DOI: 10.1101/2020.10.30.360115</identifier><language>eng</language><publisher>Cold Spring Harbor: Cold Spring Harbor Laboratory Press</publisher><subject>Antigens ; Coronaviruses ; Epitopes ; Immune response ; Immune response (cell-mediated) ; Immune response (humoral) ; Immunization ; Immunology ; Lymphocytes T ; Membrane proteins ; Vaccines ; γ-Interferon</subject><ispartof>bioRxiv, 2020-10</ispartof><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (“the License”). 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Here, we have developed PRAK-03202, the world’s first triple antigen VLP vaccine candidate in a highly characterized S. cerevisiae-based D-CryptTM platform, which induced SARS CoV-2 specific neutralizing antibodies in BALB/c mice. Immunizations using three different doses of PRAK-03202 induces antigen specific (Spike, envelope and membrane proteins) humoral response and neutralizing potential. PBMCs from convalescent patients, when exposed to PRAK-03202, showed lymphocyte proliferation and elevated IFN-γ levels suggestive of conservation of epitopes and induction of T helper 1 (Th1)–biased cellular immune responses. These data support the clinical development and testing of PRAK-03202 for use in humans. 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Here, we have developed PRAK-03202, the world’s first triple antigen VLP vaccine candidate in a highly characterized S. cerevisiae-based D-CryptTM platform, which induced SARS CoV-2 specific neutralizing antibodies in BALB/c mice. Immunizations using three different doses of PRAK-03202 induces antigen specific (Spike, envelope and membrane proteins) humoral response and neutralizing potential. PBMCs from convalescent patients, when exposed to PRAK-03202, showed lymphocyte proliferation and elevated IFN-γ levels suggestive of conservation of epitopes and induction of T helper 1 (Th1)–biased cellular immune responses. These data support the clinical development and testing of PRAK-03202 for use in humans. 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source | Coronavirus Research Database |
subjects | Antigens Coronaviruses Epitopes Immune response Immune response (cell-mediated) Immune response (humoral) Immunization Immunology Lymphocytes T Membrane proteins Vaccines γ-Interferon |
title | PRAK-03202: A triple antigen VLP vaccine candidate against SARS CoV-2 |
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