Squalene in oil-based adjuvant improves the immunogenicity of SARS-CoV-2 RBD and confirms safety in animal models
COVID-19 pandemic has accelerated the development of vaccines against its etiologic agent, SARS-CoV-2. However, the emergence of new variants of the virus lead to the generation of new alternatives to improve the current sub-unit vaccines in development. In the present report, the immunogenicity of...
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creator | Choque-Guevara, Ricardo Poma-Acevedo, Astrid Montesinos-Millán, Ricardo Rios-Matos, Dora Gutiérrez-Manchay, Kristel Montalvan-Avalos, Angela Quiñones-Garcia, Stefany Cauti-Mendoza, Maria de Grecia Agurto-Arteaga, Andres Ramirez-Ortiz, Ingrid Criollo-Orozco, Manuel Huaccachi-Gonzales, Edison Romero, Yomara K Perez-Martinez, Norma Isasi-Rivas, Gisela Sernaque-Aguilar, Yacory Villanueva-Pérez, Doris Ygnacio, Freddy Vallejos-Sánchez, Katherine Fernández-Sánchez, Manolo Guevara-Sarmiento, Luis A Fernández-Díaz, Manolo Zimic, Mirko |
description | COVID-19 pandemic has accelerated the development of vaccines against its etiologic agent, SARS-CoV-2. However, the emergence of new variants of the virus lead to the generation of new alternatives to improve the current sub-unit vaccines in development. In the present report, the immunogenicity of the Spike RBD of SARS-CoV-2 formulated with an oil-in-water emulsion and a water-in-oil emulsion with squalene was evaluated in mice and hamsters. The RBD protein was expressed in insect cells and purified by chromatography until >95% purity. The protein was shown to have the appropriate folding as determined by ELISA and flow cytometry binding assays to its receptor, as well as by its detection by hamster immune anti-S1 sera under non-reducing conditions. In immunization assays, although the cellular immune response elicited by both adjuvants were similar, the formulation based in water-in-oil emulsion and squalene generated an earlier humoral response as determined by ELISA. Similarly, this formulation was able to stimulate neutralizing antibodies in hamsters. The vaccine candidate was shown to be safe, as demonstrated by the histopathological analysis in lungs, liver and kidney. These results have shown the potential of this formulation vaccine to be evaluated in a challenge against SARS-CoV-2 and determine its ability to confer protection. |
doi_str_mv | 10.1371/journal.pone.0269823 |
format | Article |
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However, the emergence of new variants of the virus lead to the generation of new alternatives to improve the current sub-unit vaccines in development. In the present report, the immunogenicity of the Spike RBD of SARS-CoV-2 formulated with an oil-in-water emulsion and a water-in-oil emulsion with squalene was evaluated in mice and hamsters. The RBD protein was expressed in insect cells and purified by chromatography until >95% purity. The protein was shown to have the appropriate folding as determined by ELISA and flow cytometry binding assays to its receptor, as well as by its detection by hamster immune anti-S1 sera under non-reducing conditions. In immunization assays, although the cellular immune response elicited by both adjuvants were similar, the formulation based in water-in-oil emulsion and squalene generated an earlier humoral response as determined by ELISA. Similarly, this formulation was able to stimulate neutralizing antibodies in hamsters. The vaccine candidate was shown to be safe, as demonstrated by the histopathological analysis in lungs, liver and kidney. These results have shown the potential of this formulation vaccine to be evaluated in a challenge against SARS-CoV-2 and determine its ability to confer protection.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0269823</identifier><identifier>PMID: 35998134</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Adjuvants ; Animal models ; Animals ; Antibodies ; Antigens ; Biology and Life Sciences ; Chromatography ; COVID-19 ; Enzyme-linked immunosorbent assay ; Flow cytometry ; Hamsters ; Health aspects ; Immune response ; Immune response (cell-mediated) ; Immune response (humoral) ; Immune system ; Immunization ; Immunogenetics ; Immunogenicity ; Infections ; Insect cells ; Insects ; Kidneys ; Laboratories ; Medicine and Health Sciences ; Methods ; Oil ; Pandemics ; Protein folding ; Proteins ; Research and Analysis Methods ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Squalene ; Vaccines ; Viral diseases ; Viruses</subject><ispartof>PloS one, 2022-08, Vol.17 (8), p.e0269823-e0269823</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Choque-Guevara et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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However, the emergence of new variants of the virus lead to the generation of new alternatives to improve the current sub-unit vaccines in development. In the present report, the immunogenicity of the Spike RBD of SARS-CoV-2 formulated with an oil-in-water emulsion and a water-in-oil emulsion with squalene was evaluated in mice and hamsters. The RBD protein was expressed in insect cells and purified by chromatography until >95% purity. The protein was shown to have the appropriate folding as determined by ELISA and flow cytometry binding assays to its receptor, as well as by its detection by hamster immune anti-S1 sera under non-reducing conditions. In immunization assays, although the cellular immune response elicited by both adjuvants were similar, the formulation based in water-in-oil emulsion and squalene generated an earlier humoral response as determined by ELISA. Similarly, this formulation was able to stimulate neutralizing antibodies in hamsters. The vaccine candidate was shown to be safe, as demonstrated by the histopathological analysis in lungs, liver and kidney. These results have shown the potential of this formulation vaccine to be evaluated in a challenge against SARS-CoV-2 and determine its ability to confer protection.</description><subject>Adjuvants</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Biology and Life Sciences</subject><subject>Chromatography</subject><subject>COVID-19</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Flow cytometry</subject><subject>Hamsters</subject><subject>Health aspects</subject><subject>Immune response</subject><subject>Immune response (cell-mediated)</subject><subject>Immune response (humoral)</subject><subject>Immune system</subject><subject>Immunization</subject><subject>Immunogenetics</subject><subject>Immunogenicity</subject><subject>Infections</subject><subject>Insect cells</subject><subject>Insects</subject><subject>Kidneys</subject><subject>Laboratories</subject><subject>Medicine and Health 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Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choque-Guevara, Ricardo</au><au>Poma-Acevedo, Astrid</au><au>Montesinos-Millán, Ricardo</au><au>Rios-Matos, Dora</au><au>Gutiérrez-Manchay, Kristel</au><au>Montalvan-Avalos, Angela</au><au>Quiñones-Garcia, Stefany</au><au>Cauti-Mendoza, Maria de Grecia</au><au>Agurto-Arteaga, Andres</au><au>Ramirez-Ortiz, Ingrid</au><au>Criollo-Orozco, Manuel</au><au>Huaccachi-Gonzales, Edison</au><au>Romero, Yomara K</au><au>Perez-Martinez, Norma</au><au>Isasi-Rivas, Gisela</au><au>Sernaque-Aguilar, Yacory</au><au>Villanueva-Pérez, Doris</au><au>Ygnacio, Freddy</au><au>Vallejos-Sánchez, Katherine</au><au>Fernández-Sánchez, Manolo</au><au>Guevara-Sarmiento, Luis A</au><au>Fernández-Díaz, Manolo</au><au>Zimic, Mirko</au><au>Ho, Paulo Lee</au><aucorp>for the COVID-19 Working Group in Perú</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Squalene in oil-based adjuvant improves the immunogenicity of SARS-CoV-2 RBD and confirms safety in animal models</atitle><jtitle>PloS one</jtitle><date>2022-08-23</date><risdate>2022</risdate><volume>17</volume><issue>8</issue><spage>e0269823</spage><epage>e0269823</epage><pages>e0269823-e0269823</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>COVID-19 pandemic has accelerated the development of vaccines against its etiologic agent, SARS-CoV-2. However, the emergence of new variants of the virus lead to the generation of new alternatives to improve the current sub-unit vaccines in development. In the present report, the immunogenicity of the Spike RBD of SARS-CoV-2 formulated with an oil-in-water emulsion and a water-in-oil emulsion with squalene was evaluated in mice and hamsters. The RBD protein was expressed in insect cells and purified by chromatography until >95% purity. The protein was shown to have the appropriate folding as determined by ELISA and flow cytometry binding assays to its receptor, as well as by its detection by hamster immune anti-S1 sera under non-reducing conditions. In immunization assays, although the cellular immune response elicited by both adjuvants were similar, the formulation based in water-in-oil emulsion and squalene generated an earlier humoral response as determined by ELISA. Similarly, this formulation was able to stimulate neutralizing antibodies in hamsters. The vaccine candidate was shown to be safe, as demonstrated by the histopathological analysis in lungs, liver and kidney. These results have shown the potential of this formulation vaccine to be evaluated in a challenge against SARS-CoV-2 and determine its ability to confer protection.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>35998134</pmid><doi>10.1371/journal.pone.0269823</doi><tpages>e0269823</tpages><orcidid>https://orcid.org/0000-0002-7203-8847</orcidid><orcidid>https://orcid.org/0000-0002-9814-3821</orcidid><orcidid>https://orcid.org/0000-0002-6881-8234</orcidid><orcidid>https://orcid.org/0000-0002-2434-5244</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2022-08, Vol.17 (8), p.e0269823-e0269823 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2705695274 |
source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Adjuvants Animal models Animals Antibodies Antigens Biology and Life Sciences Chromatography COVID-19 Enzyme-linked immunosorbent assay Flow cytometry Hamsters Health aspects Immune response Immune response (cell-mediated) Immune response (humoral) Immune system Immunization Immunogenetics Immunogenicity Infections Insect cells Insects Kidneys Laboratories Medicine and Health Sciences Methods Oil Pandemics Protein folding Proteins Research and Analysis Methods Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Squalene Vaccines Viral diseases Viruses |
title | Squalene in oil-based adjuvant improves the immunogenicity of SARS-CoV-2 RBD and confirms safety in animal models |
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