Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages
ABSTRACT: Background: The COVID-19 pandemic remains a global health problem. As in other viral infections, the humoral immune response against SARS-CoV-2 is thought to be crucial for controlling the infection. However, the dynamic of B cells in the clinical spectrum of this disease is still controve...
- Autores:
-
Mendez Cortina, Yorjagis
Rodriguez Perea, Ana Lucía
Chvatal Medina, Mateo
Lopera, Tulio Jose
Alvarez Mesa, Natalia
Rodas Marín, Jan Karlo
Moncada, Diana Carolina
Rugeles López, Maria Teresa
Velilla, Paula Andrea
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2022
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/33233
- Acceso en línea:
- https://hdl.handle.net/10495/33233
https://www.frontiersin.org/articles/10.3389/fimmu.2022.1007068/full
- Palabra clave:
- Coronavirus Infections
Infecciones por Coronavirus
B-Lymphocytes
Linfocitos B
Antibodies, Neutralizing
Anticuerpos Neutralizantes
Severity of Illness Index
Índice de Severidad de la Enfermedad
Memory B Cells
Células B de Memoria
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages |
| title |
Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages |
| spellingShingle |
Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages Coronavirus Infections Infecciones por Coronavirus B-Lymphocytes Linfocitos B Antibodies, Neutralizing Anticuerpos Neutralizantes Severity of Illness Index Índice de Severidad de la Enfermedad Memory B Cells Células B de Memoria |
| title_short |
Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages |
| title_full |
Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages |
| title_fullStr |
Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages |
| title_full_unstemmed |
Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages |
| title_sort |
Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical Stages |
| dc.creator.fl_str_mv |
Mendez Cortina, Yorjagis Rodriguez Perea, Ana Lucía Chvatal Medina, Mateo Lopera, Tulio Jose Alvarez Mesa, Natalia Rodas Marín, Jan Karlo Moncada, Diana Carolina Rugeles López, Maria Teresa Velilla, Paula Andrea |
| dc.contributor.author.none.fl_str_mv |
Mendez Cortina, Yorjagis Rodriguez Perea, Ana Lucía Chvatal Medina, Mateo Lopera, Tulio Jose Alvarez Mesa, Natalia Rodas Marín, Jan Karlo Moncada, Diana Carolina Rugeles López, Maria Teresa Velilla, Paula Andrea |
| dc.contributor.researchgroup.spa.fl_str_mv |
Inmunovirología |
| dc.subject.decs.none.fl_str_mv |
Coronavirus Infections Infecciones por Coronavirus B-Lymphocytes Linfocitos B Antibodies, Neutralizing Anticuerpos Neutralizantes Severity of Illness Index Índice de Severidad de la Enfermedad Memory B Cells Células B de Memoria |
| topic |
Coronavirus Infections Infecciones por Coronavirus B-Lymphocytes Linfocitos B Antibodies, Neutralizing Anticuerpos Neutralizantes Severity of Illness Index Índice de Severidad de la Enfermedad Memory B Cells Células B de Memoria |
| description |
ABSTRACT: Background: The COVID-19 pandemic remains a global health problem. As in other viral infections, the humoral immune response against SARS-CoV-2 is thought to be crucial for controlling the infection. However, the dynamic of B cells in the clinical spectrum of this disease is still controversial. This study aimed to characterize B cell subsets and neutralizing responses in COVID-19 patients according to disease severity through a one-month follow-up. Methods: A cohort of 71 individuals with SARS-CoV-2 infection confirmed by RT-PCR were recruited and classified into four groups: i) asymptomatic; ii) symptomatic outpatients; iii) hospitalized in ward, and iv) intensive care unit patients (ICU). Samples were taken at days 0 (inclusion to the study), 7 and 30. B cell subsets and neutralizing antibodies were assessed using multiparametric flow cytometry and plaque reduction neutralization, respectively. Results: Older age, male gender and body mass index over 25 were common factors among hospitalized and ICU patients, compared to those with milder clinical presentations. In addition, those requiring hospitalization had more comorbidities. A significant increase in the frequencies of CD19+ cells at day 0 was observed in hospitalized and ICU patients compared to asymptomatic and symptomatic groups. Likewise, the frequency of plasmablasts was significantly increased at the first sample in the ICU group compared to the asymptomatic group, but then waned over time. The frequency of naïve B cells decreased at days 7 and 30 compared to day 0 in hospitalized and ICU patients. The neutralizing antibody titers were higher as the severity of COVID-19 increased; in asymptomatic individuals, it was strongly correlated with the percentage of IgM+ switched memory B cells, and a moderate correlation was found with plasmablasts. Conclusion: The humoral immune response is variable among SARS-CoV-2 infected people depending on the severity and time of clinical evolution. In severe COVID-19 patients, a higher plasmablast frequency and neutralizing antibody response were observed, suggesting that, despite having a robust humoral immunity, this response could be late, having a low impact on disease outcome. |
| publishDate |
2022 |
| dc.date.issued.none.fl_str_mv |
2022 |
| dc.date.accessioned.none.fl_str_mv |
2023-01-25T17:05:24Z |
| dc.date.available.none.fl_str_mv |
2023-01-25T17:05:24Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
| dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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publishedVersion |
| dc.identifier.citation.spa.fl_str_mv |
Mendez-Cortina Y, Rodriguez-Perea AL, Chvatal-Medina M, Lopera TJ, Alvarez-Mesa N, Rodas-Marín JK, Moncada DC, Rugeles MT and Velilla PA (2022) Dynamics of humoral immune response in SARS-CoV-2 infected individuals with different clinical stages. Front. Immunol. 13:1007068. doi: 10.3389/fimmu.2022.100706 |
| dc.identifier.issn.none.fl_str_mv |
1664-3224 |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/33233 |
| dc.identifier.doi.none.fl_str_mv |
10.3389/fimmu.2022.1007068 |
| dc.identifier.url.spa.fl_str_mv |
https://www.frontiersin.org/articles/10.3389/fimmu.2022.1007068/full |
| identifier_str_mv |
Mendez-Cortina Y, Rodriguez-Perea AL, Chvatal-Medina M, Lopera TJ, Alvarez-Mesa N, Rodas-Marín JK, Moncada DC, Rugeles MT and Velilla PA (2022) Dynamics of humoral immune response in SARS-CoV-2 infected individuals with different clinical stages. Front. Immunol. 13:1007068. doi: 10.3389/fimmu.2022.100706 1664-3224 10.3389/fimmu.2022.1007068 |
| url |
https://hdl.handle.net/10495/33233 https://www.frontiersin.org/articles/10.3389/fimmu.2022.1007068/full |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Front. Immunol. |
| dc.relation.citationendpage.spa.fl_str_mv |
15 |
| dc.relation.citationstartpage.spa.fl_str_mv |
1 |
| dc.relation.citationvolume.spa.fl_str_mv |
13 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Frontiers in Immunology |
| dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by/2.5/co/ |
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https://creativecommons.org/licenses/by/4.0/ |
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info:eu-repo/semantics/openAccess |
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Frontiers Research Foundation |
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Switzerland, Suiza |
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Mendez Cortina, YorjagisRodriguez Perea, Ana LucíaChvatal Medina, MateoLopera, Tulio JoseAlvarez Mesa, NataliaRodas Marín, Jan KarloMoncada, Diana CarolinaRugeles López, Maria TeresaVelilla, Paula AndreaInmunovirología2023-01-25T17:05:24Z2023-01-25T17:05:24Z2022Mendez-Cortina Y, Rodriguez-Perea AL, Chvatal-Medina M, Lopera TJ, Alvarez-Mesa N, Rodas-Marín JK, Moncada DC, Rugeles MT and Velilla PA (2022) Dynamics of humoral immune response in SARS-CoV-2 infected individuals with different clinical stages. Front. Immunol. 13:1007068. doi: 10.3389/fimmu.2022.1007061664-3224https://hdl.handle.net/10495/3323310.3389/fimmu.2022.1007068https://www.frontiersin.org/articles/10.3389/fimmu.2022.1007068/fullABSTRACT: Background: The COVID-19 pandemic remains a global health problem. As in other viral infections, the humoral immune response against SARS-CoV-2 is thought to be crucial for controlling the infection. However, the dynamic of B cells in the clinical spectrum of this disease is still controversial. This study aimed to characterize B cell subsets and neutralizing responses in COVID-19 patients according to disease severity through a one-month follow-up. Methods: A cohort of 71 individuals with SARS-CoV-2 infection confirmed by RT-PCR were recruited and classified into four groups: i) asymptomatic; ii) symptomatic outpatients; iii) hospitalized in ward, and iv) intensive care unit patients (ICU). Samples were taken at days 0 (inclusion to the study), 7 and 30. B cell subsets and neutralizing antibodies were assessed using multiparametric flow cytometry and plaque reduction neutralization, respectively. Results: Older age, male gender and body mass index over 25 were common factors among hospitalized and ICU patients, compared to those with milder clinical presentations. In addition, those requiring hospitalization had more comorbidities. A significant increase in the frequencies of CD19+ cells at day 0 was observed in hospitalized and ICU patients compared to asymptomatic and symptomatic groups. Likewise, the frequency of plasmablasts was significantly increased at the first sample in the ICU group compared to the asymptomatic group, but then waned over time. The frequency of naïve B cells decreased at days 7 and 30 compared to day 0 in hospitalized and ICU patients. The neutralizing antibody titers were higher as the severity of COVID-19 increased; in asymptomatic individuals, it was strongly correlated with the percentage of IgM+ switched memory B cells, and a moderate correlation was found with plasmablasts. Conclusion: The humoral immune response is variable among SARS-CoV-2 infected people depending on the severity and time of clinical evolution. In severe COVID-19 patients, a higher plasmablast frequency and neutralizing antibody response were observed, suggesting that, despite having a robust humoral immunity, this response could be late, having a low impact on disease outcome.COL001244415application/pdfengFrontiers Research FoundationSwitzerland, Suizahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Dynamics of Humoral Immune Response in SARS-CoV-2 Infected Individuals with different Clinical StagesArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionCoronavirus InfectionsInfecciones por CoronavirusB-LymphocytesLinfocitos BAntibodies, NeutralizingAnticuerpos NeutralizantesSeverity of Illness IndexÍndice de Severidad de la EnfermedadMemory B CellsCélulas B de MemoriaFront. 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