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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Veröffentlicht in:PloS one 2022-08, Vol.17 (8), p.e0269823-e0269823
Hauptverfasser: 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
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container_start_page e0269823
container_title PloS one
container_volume 17
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
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Edition</collection><collection>ProQuest Central China</collection><collection>Engineering 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 &gt;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>
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1932-6203
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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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