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Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients

This study monitored the long-term immune response to severe acute respiratory syndrome coronavirus (SARS-CoV)-2 infection in patients who had recovered from coronavirus disease (COVID)-19. Anti-nucleocapsid immunoglobulin G (anti-N IgG) titer in serum samples collected at a single (N = 302) or mult...

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Autores principales: Chansaenroj, Jira, Yorsaeng, Ritthideach, Posuwan, Nawarat, Puenpa, Jiratchaya, Wanlapakorn, Nasamon, Sudhinaraset, Natthinee, Sripramote, Manit, Chalongviriyalert, Piti, Jirajariyavej, Supunee, Kiatpanabhikul, Phatharaporn, Saiyarin, Jatuporn, Soudon, Chulikorn, Thienfaidee, Orawan, Palakawong Na Ayuthaya, Thitisan, Brukesawan, Chantapat, Chirathaworn, Chintana, Intharasongkroh, Duangnapa, Chaiwanichsiri, Dootchai, Issarasongkhram, Mila, Kitphati, Rungrueng, Mungaomklang, Anek, Nagavajara, Pijaya, Poovorawan, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636620/
https://www.ncbi.nlm.nih.gov/pubmed/34853374
http://dx.doi.org/10.1038/s41598-021-02659-4
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author Chansaenroj, Jira
Yorsaeng, Ritthideach
Posuwan, Nawarat
Puenpa, Jiratchaya
Wanlapakorn, Nasamon
Sudhinaraset, Natthinee
Sripramote, Manit
Chalongviriyalert, Piti
Jirajariyavej, Supunee
Kiatpanabhikul, Phatharaporn
Saiyarin, Jatuporn
Soudon, Chulikorn
Thienfaidee, Orawan
Palakawong Na Ayuthaya, Thitisan
Brukesawan, Chantapat
Chirathaworn, Chintana
Intharasongkroh, Duangnapa
Chaiwanichsiri, Dootchai
Issarasongkhram, Mila
Kitphati, Rungrueng
Mungaomklang, Anek
Nagavajara, Pijaya
Poovorawan, Yong
author_facet Chansaenroj, Jira
Yorsaeng, Ritthideach
Posuwan, Nawarat
Puenpa, Jiratchaya
Wanlapakorn, Nasamon
Sudhinaraset, Natthinee
Sripramote, Manit
Chalongviriyalert, Piti
Jirajariyavej, Supunee
Kiatpanabhikul, Phatharaporn
Saiyarin, Jatuporn
Soudon, Chulikorn
Thienfaidee, Orawan
Palakawong Na Ayuthaya, Thitisan
Brukesawan, Chantapat
Chirathaworn, Chintana
Intharasongkroh, Duangnapa
Chaiwanichsiri, Dootchai
Issarasongkhram, Mila
Kitphati, Rungrueng
Mungaomklang, Anek
Nagavajara, Pijaya
Poovorawan, Yong
author_sort Chansaenroj, Jira
collection PubMed
description This study monitored the long-term immune response to severe acute respiratory syndrome coronavirus (SARS-CoV)-2 infection in patients who had recovered from coronavirus disease (COVID)-19. Anti-nucleocapsid immunoglobulin G (anti-N IgG) titer in serum samples collected at a single (N = 302) or multiple time points (N = 229) 3–12 months after COVID-19 symptom onset or SARS-CoV-2 detection in respiratory specimens was measured by semiquantitative chemiluminescent microparticle immunoassay. The 531 patients (966 specimens) were classified according to the presence or absence of pneumonia symptoms. Anti N IgG was detected in 87.5% of patients (328/375) at 3 months, 38.6% (93/241) at 6 months, 23.7% (49/207) at 9 months, and 26.6% (38/143) at 12 months. The anti-N IgG seropositivity rate was significantly lower at 6, 9, and 12 months than at 3 months (P < 0.01) and was higher in the pneumonia group than in the non-pneumonia/asymptomatic group at 6 months (P < 0.01), 9 months (P = 0.04), and 12 months (P = 0.04). The rate started to decline 6–12 months after symptom onset. Anti-N IgG sample/cutoff index was positively correlated with age (r = 0.192, P < 0.01) but negatively correlated with interval between symptom onset and blood sampling (r =  − 0.567, P < 0.01). These findings can guide vaccine strategies in recovered COVID-19 patients.
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spelling pubmed-86366202021-12-03 Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients Chansaenroj, Jira Yorsaeng, Ritthideach Posuwan, Nawarat Puenpa, Jiratchaya Wanlapakorn, Nasamon Sudhinaraset, Natthinee Sripramote, Manit Chalongviriyalert, Piti Jirajariyavej, Supunee Kiatpanabhikul, Phatharaporn Saiyarin, Jatuporn Soudon, Chulikorn Thienfaidee, Orawan Palakawong Na Ayuthaya, Thitisan Brukesawan, Chantapat Chirathaworn, Chintana Intharasongkroh, Duangnapa Chaiwanichsiri, Dootchai Issarasongkhram, Mila Kitphati, Rungrueng Mungaomklang, Anek Nagavajara, Pijaya Poovorawan, Yong Sci Rep Article This study monitored the long-term immune response to severe acute respiratory syndrome coronavirus (SARS-CoV)-2 infection in patients who had recovered from coronavirus disease (COVID)-19. Anti-nucleocapsid immunoglobulin G (anti-N IgG) titer in serum samples collected at a single (N = 302) or multiple time points (N = 229) 3–12 months after COVID-19 symptom onset or SARS-CoV-2 detection in respiratory specimens was measured by semiquantitative chemiluminescent microparticle immunoassay. The 531 patients (966 specimens) were classified according to the presence or absence of pneumonia symptoms. Anti N IgG was detected in 87.5% of patients (328/375) at 3 months, 38.6% (93/241) at 6 months, 23.7% (49/207) at 9 months, and 26.6% (38/143) at 12 months. The anti-N IgG seropositivity rate was significantly lower at 6, 9, and 12 months than at 3 months (P < 0.01) and was higher in the pneumonia group than in the non-pneumonia/asymptomatic group at 6 months (P < 0.01), 9 months (P = 0.04), and 12 months (P = 0.04). The rate started to decline 6–12 months after symptom onset. Anti-N IgG sample/cutoff index was positively correlated with age (r = 0.192, P < 0.01) but negatively correlated with interval between symptom onset and blood sampling (r =  − 0.567, P < 0.01). These findings can guide vaccine strategies in recovered COVID-19 patients. Nature Publishing Group UK 2021-12-01 /pmc/articles/PMC8636620/ /pubmed/34853374 http://dx.doi.org/10.1038/s41598-021-02659-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chansaenroj, Jira
Yorsaeng, Ritthideach
Posuwan, Nawarat
Puenpa, Jiratchaya
Wanlapakorn, Nasamon
Sudhinaraset, Natthinee
Sripramote, Manit
Chalongviriyalert, Piti
Jirajariyavej, Supunee
Kiatpanabhikul, Phatharaporn
Saiyarin, Jatuporn
Soudon, Chulikorn
Thienfaidee, Orawan
Palakawong Na Ayuthaya, Thitisan
Brukesawan, Chantapat
Chirathaworn, Chintana
Intharasongkroh, Duangnapa
Chaiwanichsiri, Dootchai
Issarasongkhram, Mila
Kitphati, Rungrueng
Mungaomklang, Anek
Nagavajara, Pijaya
Poovorawan, Yong
Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients
title Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients
title_full Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients
title_fullStr Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients
title_full_unstemmed Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients
title_short Long-term specific IgG response to SARS-CoV-2 nucleocapsid protein in recovered COVID-19 patients
title_sort long-term specific igg response to sars-cov-2 nucleocapsid protein in recovered covid-19 patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636620/
https://www.ncbi.nlm.nih.gov/pubmed/34853374
http://dx.doi.org/10.1038/s41598-021-02659-4
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