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COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents

BACKGROUND: Studies of anti‐SARS‐CoV‐2 humoral and adaptive response in COVID‐19 non‐vaccinated pediatric convalescents are controversial and further evidence from the pediatric population are needed. OBJECTIVES: To elucidate SARS‐CoV‐2 humoral and memory B‐ and T‐cells responses in pediatric conval...

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Autores principales: Gurevich, Michael, Zilkha‐Falb, Rina, Sonis, Polina, Magalashvili, David, Dolev, Mark, Mandel, Mathilda, Menascu, Shay, Achiron, Anat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827896/
https://www.ncbi.nlm.nih.gov/pubmed/36282137
http://dx.doi.org/10.1111/pai.13863
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author Gurevich, Michael
Zilkha‐Falb, Rina
Sonis, Polina
Magalashvili, David
Dolev, Mark
Mandel, Mathilda
Menascu, Shay
Achiron, Anat
author_facet Gurevich, Michael
Zilkha‐Falb, Rina
Sonis, Polina
Magalashvili, David
Dolev, Mark
Mandel, Mathilda
Menascu, Shay
Achiron, Anat
author_sort Gurevich, Michael
collection PubMed
description BACKGROUND: Studies of anti‐SARS‐CoV‐2 humoral and adaptive response in COVID‐19 non‐vaccinated pediatric convalescents are controversial and further evidence from the pediatric population are needed. OBJECTIVES: To elucidate SARS‐CoV‐2 humoral and memory B‐ and T‐cells responses in pediatric convalescents as compared with the adult. METHODS: Blood samples were obtained from 80 non‐vaccinated, IgG‐positive, COVID‐19 convalescents (age 8.0–61.0 years), 4.0 months from onset. Frequency of responders and magnitudes of SARS‐COV‐2 IgG, memory B‐cells (MBC) and IFNg‐ and IL2‐secreting memory T‐cells (MTC) in response to immuno‐dominant peptide pools in pediatric, young adults and middle‐aged adults with onset age 8–18 years (N = 20), 19–39 years (N = 30) and 40–61 years (N = 30), respectively, were analyzed. SARS‐CoV‐2 IgG were detected by ELISA (Euroimmun, Germany). MBC, IFNg‐, IL2‐ and IFNg+IL2‐secreting MTC (IFNg‐MTC, IL2‐MTC and IFNg+IL2‐MTC) were detected using FluoroSpot (Mabtech, Sweden). RESULTS: MBC level was lower in pediatric as compared with the middle‐aged adults (median 12.75 interquartile range [IQR] 4.27–33.7 and 32.0 IQR 6.0–124.2, respectively, p = .003). MBC level in young adults was lower than in middle‐aged adults (median 18.5 IQR 1.7–43.8 and 32.0 IQR 6.0–124.2, respectively, p = .006). The level of IL2‐MTC was lower in the pediatric group as compared with middle aged‐adults (median 2.1 IQR 0–16.9 and 28.6 IQR 11–49.6, respectively, p < .03) and in young adults lower than in middle‐aged adults (median 1.45 IQR 0–18.6 and 28.6 IQR 11–49.6, respectively, p = .02). In addition, the level of IFNg‐MTC was lower in pediatric as compared with young adults (median 4.25 IQR 0.0–15.0 and 20.9 IQR 0–75.2, respectively, p = .05). The level of IgG was comparable between pediatric and both young and middle‐aged adult groups (4.82 ± 2.95, 3.70 ± 2.65 and 4.9 ± 2.94, respectively, p > .34). CONCLUSION: Non‐vaccinated COVID‐19 pediatric convalescents have lower adaptive immune responses than adults sustaining the recommendation for vaccination of the pediatric population.
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spelling pubmed-98278962023-01-10 COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents Gurevich, Michael Zilkha‐Falb, Rina Sonis, Polina Magalashvili, David Dolev, Mark Mandel, Mathilda Menascu, Shay Achiron, Anat Pediatr Allergy Immunol Original Articles BACKGROUND: Studies of anti‐SARS‐CoV‐2 humoral and adaptive response in COVID‐19 non‐vaccinated pediatric convalescents are controversial and further evidence from the pediatric population are needed. OBJECTIVES: To elucidate SARS‐CoV‐2 humoral and memory B‐ and T‐cells responses in pediatric convalescents as compared with the adult. METHODS: Blood samples were obtained from 80 non‐vaccinated, IgG‐positive, COVID‐19 convalescents (age 8.0–61.0 years), 4.0 months from onset. Frequency of responders and magnitudes of SARS‐COV‐2 IgG, memory B‐cells (MBC) and IFNg‐ and IL2‐secreting memory T‐cells (MTC) in response to immuno‐dominant peptide pools in pediatric, young adults and middle‐aged adults with onset age 8–18 years (N = 20), 19–39 years (N = 30) and 40–61 years (N = 30), respectively, were analyzed. SARS‐CoV‐2 IgG were detected by ELISA (Euroimmun, Germany). MBC, IFNg‐, IL2‐ and IFNg+IL2‐secreting MTC (IFNg‐MTC, IL2‐MTC and IFNg+IL2‐MTC) were detected using FluoroSpot (Mabtech, Sweden). RESULTS: MBC level was lower in pediatric as compared with the middle‐aged adults (median 12.75 interquartile range [IQR] 4.27–33.7 and 32.0 IQR 6.0–124.2, respectively, p = .003). MBC level in young adults was lower than in middle‐aged adults (median 18.5 IQR 1.7–43.8 and 32.0 IQR 6.0–124.2, respectively, p = .006). The level of IL2‐MTC was lower in the pediatric group as compared with middle aged‐adults (median 2.1 IQR 0–16.9 and 28.6 IQR 11–49.6, respectively, p < .03) and in young adults lower than in middle‐aged adults (median 1.45 IQR 0–18.6 and 28.6 IQR 11–49.6, respectively, p = .02). In addition, the level of IFNg‐MTC was lower in pediatric as compared with young adults (median 4.25 IQR 0.0–15.0 and 20.9 IQR 0–75.2, respectively, p = .05). The level of IgG was comparable between pediatric and both young and middle‐aged adult groups (4.82 ± 2.95, 3.70 ± 2.65 and 4.9 ± 2.94, respectively, p > .34). CONCLUSION: Non‐vaccinated COVID‐19 pediatric convalescents have lower adaptive immune responses than adults sustaining the recommendation for vaccination of the pediatric population. John Wiley and Sons Inc. 2022-10-06 2022-10 /pmc/articles/PMC9827896/ /pubmed/36282137 http://dx.doi.org/10.1111/pai.13863 Text en © 2022 The Authors. Pediatric Allergy and Immunology published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Gurevich, Michael
Zilkha‐Falb, Rina
Sonis, Polina
Magalashvili, David
Dolev, Mark
Mandel, Mathilda
Menascu, Shay
Achiron, Anat
COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents
title COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents
title_full COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents
title_fullStr COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents
title_full_unstemmed COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents
title_short COVID‐19 Alpha Variant (B.1.1.7): Humoral, memory B and T cells in COVID‐19 pediatric convalescents
title_sort covid‐19 alpha variant (b.1.1.7): humoral, memory b and t cells in covid‐19 pediatric convalescents
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827896/
https://www.ncbi.nlm.nih.gov/pubmed/36282137
http://dx.doi.org/10.1111/pai.13863
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