Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Digital do Instituto Evandro Chagas (Patuá) |
Texto Completo: | https://patua.iec.gov.br/handle/iec/6822 |
Resumo: | The first case of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), in Brazil was diagnosed on February 26, 2020. Due to the important epidemiological impact of COVID-19, the present study aimed to analyze the specificity of IgG antibody responses to the S1, S2 and N proteins of SARS-CoV-2 in different COVID-19 clinical profiles. This study enrolled 136 individuals who were diagnosed with or without COVID-19 based on clinical findings and laboratory results and classified as asymptomatic or as having mild, moderate or severe disease. Data collection was performed through a semistructured questionnaire to obtain demographic information and main clinical manifestations. IgG antibody responses to the S1 and S2 subunits of the spike (S) protein and the nucleocapsid (N) protein were evaluated using an enzyme-linked immunosorbent assay (ELISA) according to the manufacturer’s instructions. The results showed that among the participants, 87.5% (119/136) exhibited IgG responses to the S1 subunit and 88.25% (120/136) to N. Conversely, only 14.44% of the subjects (21/136) displayed S2 subunit responses. When analyzing the IgG antibody response while considering the different proteins of the virus, patients with severe disease had significantly higher antibody responses to N and S1 than asymptomatic individuals (p ≤ 0.0001), whereas most of the participants had low antibody titers against the S2 subunit. In addition, individuals with long COVID-19 showed a greater IgG response profile than those with symptomatology of a short duration. Based on the results of this study, it is concluded that levels of IgG antibodies may be related to the clinical evolution of COVID-19, with high levels of IgG antibodies against S1 and N in severe cases and in individuals with long COVID-19. |
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Soares, Sinei RamosTorres, Maria Karoliny da SilvaLima, Sandra SouzaSarges, Kevin Matheus Lima deSantos, Erika Ferreira dosBritto, Mioni Thieli Figueiredo Magalhães deSilva, Andréa Luciana Soares daLeite, Mauro de MeiraCosta, Flávia Póvoa daCantanhede, Marcos Henrique DamascenoSilva, Rosilene daVeríssimo, Adriana de Oliveira LameiraVallinoto, Izaura Maria Vieira CayresFeitosa, Rosimar Neris MartinsQuaresma, Juarez Antônio SimõesChaves, Tânia do Socorro SouzaViana, Giselle Maria RachidFalcão, Luiz Fábio MagnoSantos, Eduardo José Melo dosVallinoto, Antonio Carlos RosárioSilva, Andréa Nazaré Monteiro Rangel da2023-05-15T17:46:43Z2023-05-15T17:46:43Z2023SOARES, Sinei Ramos et al. Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles. Viruses, v. 15, n. 4, p. 1-12, 2023. DOI: https://doi.org/10.3390/v15040898. Disponível em: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141342/pdf/viruses-15-00898.pdf1999-4915https://patua.iec.gov.br/handle/iec/682210.3390/v15040898The first case of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), in Brazil was diagnosed on February 26, 2020. Due to the important epidemiological impact of COVID-19, the present study aimed to analyze the specificity of IgG antibody responses to the S1, S2 and N proteins of SARS-CoV-2 in different COVID-19 clinical profiles. This study enrolled 136 individuals who were diagnosed with or without COVID-19 based on clinical findings and laboratory results and classified as asymptomatic or as having mild, moderate or severe disease. Data collection was performed through a semistructured questionnaire to obtain demographic information and main clinical manifestations. IgG antibody responses to the S1 and S2 subunits of the spike (S) protein and the nucleocapsid (N) protein were evaluated using an enzyme-linked immunosorbent assay (ELISA) according to the manufacturer’s instructions. The results showed that among the participants, 87.5% (119/136) exhibited IgG responses to the S1 subunit and 88.25% (120/136) to N. Conversely, only 14.44% of the subjects (21/136) displayed S2 subunit responses. When analyzing the IgG antibody response while considering the different proteins of the virus, patients with severe disease had significantly higher antibody responses to N and S1 than asymptomatic individuals (p ≤ 0.0001), whereas most of the participants had low antibody titers against the S2 subunit. In addition, individuals with long COVID-19 showed a greater IgG response profile than those with symptomatology of a short duration. Based on the results of this study, it is concluded that levels of IgG antibodies may be related to the clinical evolution of COVID-19, with high levels of IgG antibodies against S1 and N in severe cases and in individuals with long COVID-19.National Council for Scientific and Technological Development (CNPQ #401235/2020-3; #302935/2021-5), Fundação Amazônia de Amparo a Estudos e Pesquisa do Pará (FAPESPA #005/2020 and #006/2020) and Secretaria de Ciência, Tecnologia e Educação Superior, Profissional e Tecnológica (SECTET #09/2021)Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Virologia. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Virologia. Belém, PA, Brazil / Universidade Federal do Pará. Programa de Pós-Graduação em Biologia de Agentes Infecciosos e Parasitários. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Virologia. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Hospital Adventista de Belém. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Virologia. Belém, PA, Brazil / Universidade Federal do Pará. Programa de Pós-Graduação em Biologia de Agentes Infecciosos e Parasitários. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Virologia. Belém, PA, Brazil / Universidade Federal do Pará. Programa de Pós-Graduação em Biologia de Agentes Infecciosos e Parasitários. Belém, PA, Brazil.Universidade Federal do Pará. Programa de Pós-Graduação em Biologia de Agentes Infecciosos e Parasitários. Belém, PA, Brazil / Universidade do Estado do Pará. Centro de Ciências Biológicas e da Saúde. Belém, PA, Brazil.Ministério da Saúde. Secretaria de Vigilância em Saúde e Ambiente. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Universidade Federal do Pará. Programa de Pós-Graduação em Biologia de Agentes Infecciosos e Parasitários. Belém, PA, Brazil / Ministério da Saúde. Secretaria de Vigilância em Saúde e Ambiente. Instituto Evandro Chagas. Ananindeua, PA, Brasil.Universidade do Estado do Pará. Centro de Ciências Biológicas e da Saúde. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Genética de Doenças Complexas. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Virologia. Belém, PA, Brazil.Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Virologia. Belém, PA, Brazil / Universidade Federal do Pará. Programa de Pós-Graduação em Biologia de Agentes Infecciosos e Parasitários. 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dc.title.pt_BR.fl_str_mv |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles |
title |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles |
spellingShingle |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles Soares, Sinei Ramos COVID-19 / imunologia SARS-CoV-2 / imunologia Anticorpos / imunologia Receptores de IgG / imunologia Imunidade Humoral |
title_short |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles |
title_full |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles |
title_fullStr |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles |
title_full_unstemmed |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles |
title_sort |
Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles |
author |
Soares, Sinei Ramos |
author_facet |
Soares, Sinei Ramos Torres, Maria Karoliny da Silva Lima, Sandra Souza Sarges, Kevin Matheus Lima de Santos, Erika Ferreira dos Britto, Mioni Thieli Figueiredo Magalhães de Silva, Andréa Luciana Soares da Leite, Mauro de Meira Costa, Flávia Póvoa da Cantanhede, Marcos Henrique Damasceno Silva, Rosilene da Veríssimo, Adriana de Oliveira Lameira Vallinoto, Izaura Maria Vieira Cayres Feitosa, Rosimar Neris Martins Quaresma, Juarez Antônio Simões Chaves, Tânia do Socorro Souza Viana, Giselle Maria Rachid Falcão, Luiz Fábio Magno Santos, Eduardo José Melo dos Vallinoto, Antonio Carlos Rosário Silva, Andréa Nazaré Monteiro Rangel da |
author_role |
author |
author2 |
Torres, Maria Karoliny da Silva Lima, Sandra Souza Sarges, Kevin Matheus Lima de Santos, Erika Ferreira dos Britto, Mioni Thieli Figueiredo Magalhães de Silva, Andréa Luciana Soares da Leite, Mauro de Meira Costa, Flávia Póvoa da Cantanhede, Marcos Henrique Damasceno Silva, Rosilene da Veríssimo, Adriana de Oliveira Lameira Vallinoto, Izaura Maria Vieira Cayres Feitosa, Rosimar Neris Martins Quaresma, Juarez Antônio Simões Chaves, Tânia do Socorro Souza Viana, Giselle Maria Rachid Falcão, Luiz Fábio Magno Santos, Eduardo José Melo dos Vallinoto, Antonio Carlos Rosário Silva, Andréa Nazaré Monteiro Rangel da |
author2_role |
author author author author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Soares, Sinei Ramos Torres, Maria Karoliny da Silva Lima, Sandra Souza Sarges, Kevin Matheus Lima de Santos, Erika Ferreira dos Britto, Mioni Thieli Figueiredo Magalhães de Silva, Andréa Luciana Soares da Leite, Mauro de Meira Costa, Flávia Póvoa da Cantanhede, Marcos Henrique Damasceno Silva, Rosilene da Veríssimo, Adriana de Oliveira Lameira Vallinoto, Izaura Maria Vieira Cayres Feitosa, Rosimar Neris Martins Quaresma, Juarez Antônio Simões Chaves, Tânia do Socorro Souza Viana, Giselle Maria Rachid Falcão, Luiz Fábio Magno Santos, Eduardo José Melo dos Vallinoto, Antonio Carlos Rosário Silva, Andréa Nazaré Monteiro Rangel da |
dc.subject.decsPrimary.pt_BR.fl_str_mv |
COVID-19 / imunologia SARS-CoV-2 / imunologia Anticorpos / imunologia Receptores de IgG / imunologia Imunidade Humoral |
topic |
COVID-19 / imunologia SARS-CoV-2 / imunologia Anticorpos / imunologia Receptores de IgG / imunologia Imunidade Humoral |
description |
The first case of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), in Brazil was diagnosed on February 26, 2020. Due to the important epidemiological impact of COVID-19, the present study aimed to analyze the specificity of IgG antibody responses to the S1, S2 and N proteins of SARS-CoV-2 in different COVID-19 clinical profiles. This study enrolled 136 individuals who were diagnosed with or without COVID-19 based on clinical findings and laboratory results and classified as asymptomatic or as having mild, moderate or severe disease. Data collection was performed through a semistructured questionnaire to obtain demographic information and main clinical manifestations. IgG antibody responses to the S1 and S2 subunits of the spike (S) protein and the nucleocapsid (N) protein were evaluated using an enzyme-linked immunosorbent assay (ELISA) according to the manufacturer’s instructions. The results showed that among the participants, 87.5% (119/136) exhibited IgG responses to the S1 subunit and 88.25% (120/136) to N. Conversely, only 14.44% of the subjects (21/136) displayed S2 subunit responses. When analyzing the IgG antibody response while considering the different proteins of the virus, patients with severe disease had significantly higher antibody responses to N and S1 than asymptomatic individuals (p ≤ 0.0001), whereas most of the participants had low antibody titers against the S2 subunit. In addition, individuals with long COVID-19 showed a greater IgG response profile than those with symptomatology of a short duration. Based on the results of this study, it is concluded that levels of IgG antibodies may be related to the clinical evolution of COVID-19, with high levels of IgG antibodies against S1 and N in severe cases and in individuals with long COVID-19. |
publishDate |
2023 |
dc.date.accessioned.fl_str_mv |
2023-05-15T17:46:43Z |
dc.date.available.fl_str_mv |
2023-05-15T17:46:43Z |
dc.date.issued.fl_str_mv |
2023 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
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publishedVersion |
dc.identifier.citation.fl_str_mv |
SOARES, Sinei Ramos et al. Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles. Viruses, v. 15, n. 4, p. 1-12, 2023. DOI: https://doi.org/10.3390/v15040898. Disponível em: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141342/pdf/viruses-15-00898.pdf |
dc.identifier.uri.fl_str_mv |
https://patua.iec.gov.br/handle/iec/6822 |
dc.identifier.issn.-.fl_str_mv |
1999-4915 |
dc.identifier.doi.pt_BR.fl_str_mv |
10.3390/v15040898 |
identifier_str_mv |
SOARES, Sinei Ramos et al. Antibody response to the SARS-CoV-2 spike and nucleocapsid proteins in patients with different COVID-19 clinical profiles. Viruses, v. 15, n. 4, p. 1-12, 2023. DOI: https://doi.org/10.3390/v15040898. Disponível em: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141342/pdf/viruses-15-00898.pdf 1999-4915 10.3390/v15040898 |
url |
https://patua.iec.gov.br/handle/iec/6822 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
MDPI |
publisher.none.fl_str_mv |
MDPI |
dc.source.none.fl_str_mv |
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Repositório Digital do Instituto Evandro Chagas (Patuá) - Instituto Evandro Chagas (IEC) |
repository.mail.fl_str_mv |
clariceneta@iec.gov.br || Biblioteca@iec.gov.br |
_version_ |
1809190059303239680 |