Evaluating the immunogenicity of gold nanoparticles conjugated RBD with Freund's adjuvant as a potential vaccine against SARS-CoV-2

and Introduction: SARS-CoV-2 is currently considered as the most challenging issue in the field of health and medicine by causing a global pandemic. Vaccines are counted as a promising candidate to terminate this deadly pandemic. Various structural proteins in SARS-CoV-2 have recently drawn attentio...

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Veröffentlicht in:Microbial pathogenesis 2022-09, Vol.170, p.105687-105687, Article 105687
Hauptverfasser: Moshref Javadi, Mahtab, Taghdisi Hosseinzadeh, Mozhgan, Soleimani, Neda, Rommasi, Foad
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container_start_page 105687
container_title Microbial pathogenesis
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creator Moshref Javadi, Mahtab
Taghdisi Hosseinzadeh, Mozhgan
Soleimani, Neda
Rommasi, Foad
description and Introduction: SARS-CoV-2 is currently considered as the most challenging issue in the field of health and medicine by causing a global pandemic. Vaccines are counted as a promising candidate to terminate this deadly pandemic. Various structural proteins in SARS-CoV-2 have recently drawn attention to be utilized as candidate vaccines to stimulate immune responses against COVID-19. In current study, the RBD protein was cloned and expressed in E. coli host. Then, the expressed RBD protein was purified and its characterizations were evaluated through various methods. Gold nanoparticles, which were utilized as a carrier for candidate Nano-vaccine, were synthesized via oxidation-reduction reaction. While Gold NPs-conjugated RBD was injected into the second treatment group, in the first candidate vaccine, RBD was injected into the first treatment group solely. Complete and Incomplete Freud's Adjuvant were also utilized for both treatment groups to enhance the immune responses against RBD antigen. Immunizations were repeated 2 times in 14-day intervals to boost the immune system of BALB/c mice. The humoral and cell-mediated immune responses were examined through immune and cytokine assays. Our outcomes demonstrate that strong short-term humoral immunity (IgM) was induced in both the first and second treatment group, while long-term humoral responses (IgG) were only observed in the second treatment group. While stronger short- and long-term humoral (IgM and IgG, respectively) were observed in the second treatment group, particular cytokines production (TNF-ɑ and IFN-γ) as a marker of cell-mediated responses were significantly higher in the first treatment group. Our study results show the high potentiality of RBD protein as an appropriate stimulating antigen in vaccine synthesis and testifies RBD-based candidate vaccines to control the COVID-19 pandemic. Our outcomes also recommend that Nano-vaccines can be more suitable candidates when stronger long-term immune responses matter. •As one critical in medical fields, SARS-CoV-2 has drawn scientists’ attention to find efficient solutions to cope with it.•Traditional vaccine manufacturing technologies are typically accompanied by some unignorably drawbacks.•Nanoparticles, particularly gold nanoparticles (GNPs), can strongly activate immune system against different pathogens.•The application of Nano vaccines utilizing novel nanoparticles like GNPs, can eliminate the cons of other types of vaccines.•In this research,
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Our outcomes also recommend that Nano-vaccines can be more suitable candidates when stronger long-term immune responses matter. •As one critical in medical fields, SARS-CoV-2 has drawn scientists’ attention to find efficient solutions to cope with it.•Traditional vaccine manufacturing technologies are typically accompanied by some unignorably drawbacks.•Nanoparticles, particularly gold nanoparticles (GNPs), can strongly activate immune system against different pathogens.•The application of Nano vaccines utilizing novel nanoparticles like GNPs, can eliminate the cons of other types of vaccines.•In this research, the outcomes prove the higher efficacy of Nano vaccines compared to a protein subunit vaccine.</description><identifier>ISSN: 0882-4010</identifier><identifier>ISSN: 1096-1208</identifier><identifier>EISSN: 1096-1208</identifier><identifier>DOI: 10.1016/j.micpath.2022.105687</identifier><identifier>PMID: 35917987</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adjuvants, Immunologic ; Animals ; Antibodies, Neutralizing ; Antibodies, Viral ; COVID-19 - prevention &amp; control ; COVID-19 vaccine ; COVID-19 Vaccines ; Escherichia coli - genetics ; Freund's Adjuvant ; Gold ; Gold nanoparticles ; Humans ; Immunogenic proteins ; Immunogenicity, Vaccine ; Immunoglobulin G ; Immunoglobulin M ; Metal Nanoparticles ; Mice ; Mice, Inbred BALB C ; Nano-vaccines ; Pandemics ; RBD protein ; SARS-CoV-2 ; Viral Vaccines</subject><ispartof>Microbial pathogenesis, 2022-09, Vol.170, p.105687-105687, Article 105687</ispartof><rights>2022 Elsevier Ltd</rights><rights>Copyright © 2022 Elsevier Ltd. 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Our outcomes also recommend that Nano-vaccines can be more suitable candidates when stronger long-term immune responses matter. •As one critical in medical fields, SARS-CoV-2 has drawn scientists’ attention to find efficient solutions to cope with it.•Traditional vaccine manufacturing technologies are typically accompanied by some unignorably drawbacks.•Nanoparticles, particularly gold nanoparticles (GNPs), can strongly activate immune system against different pathogens.•The application of Nano vaccines utilizing novel nanoparticles like GNPs, can eliminate the cons of other types of vaccines.•In this research, the outcomes prove the higher efficacy of Nano vaccines compared to a protein subunit vaccine.</description><subject>Adjuvants, Immunologic</subject><subject>Animals</subject><subject>Antibodies, Neutralizing</subject><subject>Antibodies, Viral</subject><subject>COVID-19 - prevention &amp; control</subject><subject>COVID-19 vaccine</subject><subject>COVID-19 Vaccines</subject><subject>Escherichia coli - genetics</subject><subject>Freund's Adjuvant</subject><subject>Gold</subject><subject>Gold nanoparticles</subject><subject>Humans</subject><subject>Immunogenic proteins</subject><subject>Immunogenicity, Vaccine</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Metal Nanoparticles</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Nano-vaccines</subject><subject>Pandemics</subject><subject>RBD protein</subject><subject>SARS-CoV-2</subject><subject>Viral Vaccines</subject><issn>0882-4010</issn><issn>1096-1208</issn><issn>1096-1208</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhiMEotvCI4B8g0sW23Fi5wIqSwtIlZBa4GrN2pOso8Texk5Qz31xUu1SwYnTjGb--Wc0X5a9YnTNKKvedevBmT2k3ZpTzpdaWSn5JFsxWlc541Q9zVZUKZ4LyuhJdhpjRymtRVE_z06KsmayVnKV3V_M0E-QnG9J2iFxwzD50KJ3xqU7EhrSht4SDz7sYUzO9BiJCb6bWkhoyfXHT-SXSztyOeLk7ZtIwHbTDD4RWHKyDwl9ctCTGYxxHgm04HxM5Ob8-ibfhJ85f5E9a6CP-PIYz7IflxffN1_yq2-fv27Or3JT1DLlVmBphNiCrURBm0Y0WJWVkRaqktXSgEDOrGSFUJZvDVdSUagaVdAtU0LK4ix7f_DdT9sBrVkOG6HX-9ENMN7pAE7_2_Fup9sw67ooakb5YvD2aDCG2wlj0oOLBvsePIYpal7VspKFoGqRlgepGUOMIzaPaxjVDwB1p48A9QNAfQC4zL3--8bHqT_EFsGHgwCXT80ORx2NQ2_QuhFN0ja4_6z4DQLpsZA</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Moshref Javadi, Mahtab</creator><creator>Taghdisi Hosseinzadeh, Mozhgan</creator><creator>Soleimani, Neda</creator><creator>Rommasi, Foad</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7189-170X</orcidid></search><sort><creationdate>20220901</creationdate><title>Evaluating the immunogenicity of gold nanoparticles conjugated RBD with Freund's adjuvant as a potential vaccine against SARS-CoV-2</title><author>Moshref Javadi, Mahtab ; 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Vaccines are counted as a promising candidate to terminate this deadly pandemic. Various structural proteins in SARS-CoV-2 have recently drawn attention to be utilized as candidate vaccines to stimulate immune responses against COVID-19. In current study, the RBD protein was cloned and expressed in E. coli host. Then, the expressed RBD protein was purified and its characterizations were evaluated through various methods. Gold nanoparticles, which were utilized as a carrier for candidate Nano-vaccine, were synthesized via oxidation-reduction reaction. While Gold NPs-conjugated RBD was injected into the second treatment group, in the first candidate vaccine, RBD was injected into the first treatment group solely. Complete and Incomplete Freud's Adjuvant were also utilized for both treatment groups to enhance the immune responses against RBD antigen. Immunizations were repeated 2 times in 14-day intervals to boost the immune system of BALB/c mice. The humoral and cell-mediated immune responses were examined through immune and cytokine assays. Our outcomes demonstrate that strong short-term humoral immunity (IgM) was induced in both the first and second treatment group, while long-term humoral responses (IgG) were only observed in the second treatment group. While stronger short- and long-term humoral (IgM and IgG, respectively) were observed in the second treatment group, particular cytokines production (TNF-ɑ and IFN-γ) as a marker of cell-mediated responses were significantly higher in the first treatment group. Our study results show the high potentiality of RBD protein as an appropriate stimulating antigen in vaccine synthesis and testifies RBD-based candidate vaccines to control the COVID-19 pandemic. 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subjects Adjuvants, Immunologic
Animals
Antibodies, Neutralizing
Antibodies, Viral
COVID-19 - prevention & control
COVID-19 vaccine
COVID-19 Vaccines
Escherichia coli - genetics
Freund's Adjuvant
Gold
Gold nanoparticles
Humans
Immunogenic proteins
Immunogenicity, Vaccine
Immunoglobulin G
Immunoglobulin M
Metal Nanoparticles
Mice
Mice, Inbred BALB C
Nano-vaccines
Pandemics
RBD protein
SARS-CoV-2
Viral Vaccines
title Evaluating the immunogenicity of gold nanoparticles conjugated RBD with Freund's adjuvant as a potential vaccine against SARS-CoV-2
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