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Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study

Background: SARS-CoV-2 enters the body through inhalation or self-inoculation to mucosal surfaces. The kinetics of the ocular and nasal mucosal-specific-immunoglobulin A(IgA) responses remain under-studied. Methods: Conjunctival fluid (CF, n = 140) and nasal epithelial lining fluid (NELF, n = 424) o...

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Autores principales: Chan, Renee W. Y., Chan, Kate C. C., Lui, Grace C. Y., Tsun, Joseph G. S., Chan, Kathy Y. Y., Yip, Jasmine S. K., Liu, Shaojun, Yu, Michelle W. L., Ng, Rita W. Y., Chong, Kelvin K. L., Wang, Maggie H., Chan, Paul K. S., Li, Albert M., Lam, Hugh Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026526/
https://www.ncbi.nlm.nih.gov/pubmed/35456072
http://dx.doi.org/10.3390/pathogens11040397
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author Chan, Renee W. Y.
Chan, Kate C. C.
Lui, Grace C. Y.
Tsun, Joseph G. S.
Chan, Kathy Y. Y.
Yip, Jasmine S. K.
Liu, Shaojun
Yu, Michelle W. L.
Ng, Rita W. Y.
Chong, Kelvin K. L.
Wang, Maggie H.
Chan, Paul K. S.
Li, Albert M.
Lam, Hugh Simon
author_facet Chan, Renee W. Y.
Chan, Kate C. C.
Lui, Grace C. Y.
Tsun, Joseph G. S.
Chan, Kathy Y. Y.
Yip, Jasmine S. K.
Liu, Shaojun
Yu, Michelle W. L.
Ng, Rita W. Y.
Chong, Kelvin K. L.
Wang, Maggie H.
Chan, Paul K. S.
Li, Albert M.
Lam, Hugh Simon
author_sort Chan, Renee W. Y.
collection PubMed
description Background: SARS-CoV-2 enters the body through inhalation or self-inoculation to mucosal surfaces. The kinetics of the ocular and nasal mucosal-specific-immunoglobulin A(IgA) responses remain under-studied. Methods: Conjunctival fluid (CF, n = 140) and nasal epithelial lining fluid (NELF, n = 424) obtained by paper strips and plasma (n = 153) were collected longitudinally from SARS-CoV-2 paediatric (n = 34) and adult (n = 47) patients. The SARS-CoV-2 spike protein 1(S1)-specific mucosal antibody levels in COVID-19 patients, from hospital admission to six months post-diagnosis, were assessed. Results: The mucosal antibody was IgA-predominant. In the NELF of asymptomatic paediatric patients, S1-specific IgA was induced as early as the first four days post-diagnosis. Their plasma S1-specific IgG levels were higher than in symptomatic patients in the second week after diagnosis. The IgA and IgG levels correlated positively with the surrogate neutralization readout. The detectable NELF “receptor-blocking” S1-specific IgA in the first week after diagnosis correlated with a rapid decline in viral load. Conclusions: Early and intense nasal S1-specific IgA levels link to a rapid decrease in viral load. Our results provide insights into the role of mucosal immunity in SARS-CoV-2 exposure and protection. There may be a role of NELF IgA in the screening and diagnosis of SARS-CoV-2 infection.
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spelling pubmed-90265262022-04-23 Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study Chan, Renee W. Y. Chan, Kate C. C. Lui, Grace C. Y. Tsun, Joseph G. S. Chan, Kathy Y. Y. Yip, Jasmine S. K. Liu, Shaojun Yu, Michelle W. L. Ng, Rita W. Y. Chong, Kelvin K. L. Wang, Maggie H. Chan, Paul K. S. Li, Albert M. Lam, Hugh Simon Pathogens Article Background: SARS-CoV-2 enters the body through inhalation or self-inoculation to mucosal surfaces. The kinetics of the ocular and nasal mucosal-specific-immunoglobulin A(IgA) responses remain under-studied. Methods: Conjunctival fluid (CF, n = 140) and nasal epithelial lining fluid (NELF, n = 424) obtained by paper strips and plasma (n = 153) were collected longitudinally from SARS-CoV-2 paediatric (n = 34) and adult (n = 47) patients. The SARS-CoV-2 spike protein 1(S1)-specific mucosal antibody levels in COVID-19 patients, from hospital admission to six months post-diagnosis, were assessed. Results: The mucosal antibody was IgA-predominant. In the NELF of asymptomatic paediatric patients, S1-specific IgA was induced as early as the first four days post-diagnosis. Their plasma S1-specific IgG levels were higher than in symptomatic patients in the second week after diagnosis. The IgA and IgG levels correlated positively with the surrogate neutralization readout. The detectable NELF “receptor-blocking” S1-specific IgA in the first week after diagnosis correlated with a rapid decline in viral load. Conclusions: Early and intense nasal S1-specific IgA levels link to a rapid decrease in viral load. Our results provide insights into the role of mucosal immunity in SARS-CoV-2 exposure and protection. There may be a role of NELF IgA in the screening and diagnosis of SARS-CoV-2 infection. MDPI 2022-03-24 /pmc/articles/PMC9026526/ /pubmed/35456072 http://dx.doi.org/10.3390/pathogens11040397 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chan, Renee W. Y.
Chan, Kate C. C.
Lui, Grace C. Y.
Tsun, Joseph G. S.
Chan, Kathy Y. Y.
Yip, Jasmine S. K.
Liu, Shaojun
Yu, Michelle W. L.
Ng, Rita W. Y.
Chong, Kelvin K. L.
Wang, Maggie H.
Chan, Paul K. S.
Li, Albert M.
Lam, Hugh Simon
Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study
title Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study
title_full Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study
title_fullStr Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study
title_full_unstemmed Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study
title_short Mucosal Antibody Response to SARS-CoV-2 in Paediatric and Adult Patients: A Longitudinal Study
title_sort mucosal antibody response to sars-cov-2 in paediatric and adult patients: a longitudinal study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026526/
https://www.ncbi.nlm.nih.gov/pubmed/35456072
http://dx.doi.org/10.3390/pathogens11040397
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