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SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma

BACKGROUND: Asthma patients potentially have impaired adaptive immunity to virus infection. The levels of SARS-CoV-2-specific adaptive immunity between COVID-19 survivors with and without asthma are presently unclear. METHODS: COVID-19 survivors (patients with asthma n=11, with allergies n=8, and CO...

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Autores principales: Chen, Li, Yue, Junqing, Zhang, Shengding, Bai, Wenxue, Qin, Lu, Zhang, Cong, Wu, Bihao, Li, Moxuan, Xu, Shuyun, Jiang, Qing, Yang, Lin, Xu, Qingxiu, Zhu, Rongfei, Xie, Min, Gong, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339657/
https://www.ncbi.nlm.nih.gov/pubmed/35924252
http://dx.doi.org/10.3389/fimmu.2022.947724
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author Chen, Li
Yue, Junqing
Zhang, Shengding
Bai, Wenxue
Qin, Lu
Zhang, Cong
Wu, Bihao
Li, Moxuan
Xu, Shuyun
Jiang, Qing
Yang, Lin
Xu, Qingxiu
Zhu, Rongfei
Xie, Min
Gong, Rui
author_facet Chen, Li
Yue, Junqing
Zhang, Shengding
Bai, Wenxue
Qin, Lu
Zhang, Cong
Wu, Bihao
Li, Moxuan
Xu, Shuyun
Jiang, Qing
Yang, Lin
Xu, Qingxiu
Zhu, Rongfei
Xie, Min
Gong, Rui
author_sort Chen, Li
collection PubMed
description BACKGROUND: Asthma patients potentially have impaired adaptive immunity to virus infection. The levels of SARS-CoV-2-specific adaptive immunity between COVID-19 survivors with and without asthma are presently unclear. METHODS: COVID-19 survivors (patients with asthma n=11, with allergies n=8, and COVID-19 only n=17) and non-COVID-19 individuals (asthmatic patients n=10 and healthy controls n=9) were included. The COVID-19 patients were followed up at about 8 months and 16 months after discharge. The clinical characteristics, lymphocyte subsets, memory T cells, and humoral immunity including SARS-CoV-2 specific antibodies, SARS-CoV-2 pseudotyped virus neutralization assay, and memory B cells were analyzed in these subjects. RESULTS: The strength of virus-specific T cell response in COVID-19 survivors was positively correlated with the percentage of blood eosinophils and Treg cells (r=0.4007, p=0.0188; and r=0.4435, p=0.0086 respectively) at 8-month follow-up. There were no statistical differences in the levels of SARS-CoV-2-specific T cell response between the COVID-19 survivors with, and without, asthma. Compared to those without asthma, the COVID-19 with asthma survivors had higher levels of SARS-CoV-2-specific neutralizing antibodies (NAbs) at the 8-month follow-up (p<0.05). Moreover, the level of NAbs in COVID-19 survivors was positively correlated with the percentage of Treg and cTfh2 cells (r=0.5037, p=0.002; and r=0.4846, p=0.0141), and negatively correlated with the percentage of Th1 and Th17 cells (r=-0.5701, p=0.0003; and r=-0.3656, p=0.0308), the ratio of Th1/Th2, Th17/Treg, and cTfh1/cTfh2 cell (r=-0.5356, r=-0.5947, r=-0.4485; all p<0.05). The decay rate of NAbs in the COVID-19 survivors with asthma was not significantly different from that of those without asthma at 16-month follow-up. CONCLUSION: The level of SARS-CoV-2-specific NAbs in COVID-19 survivors with asthma was higher than that of those without asthma at 8-month follow-up. The SARS-CoV-2-specific T cell immunity was associated with blood eosinophils and Treg percentages. The SARS-CoV-2-specific humoral immunity was closely associated with cTfh2/cTfh1 imbalance and Treg/Th17 ratio. According to the findings, asthmatic patients in COVID-19 convalescent period may benefit from an enhanced specific humoral immunity, which associates with skewed Th2/Th1 and Treg/Th17 immune.
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spelling pubmed-93396572022-08-02 SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma Chen, Li Yue, Junqing Zhang, Shengding Bai, Wenxue Qin, Lu Zhang, Cong Wu, Bihao Li, Moxuan Xu, Shuyun Jiang, Qing Yang, Lin Xu, Qingxiu Zhu, Rongfei Xie, Min Gong, Rui Front Immunol Immunology BACKGROUND: Asthma patients potentially have impaired adaptive immunity to virus infection. The levels of SARS-CoV-2-specific adaptive immunity between COVID-19 survivors with and without asthma are presently unclear. METHODS: COVID-19 survivors (patients with asthma n=11, with allergies n=8, and COVID-19 only n=17) and non-COVID-19 individuals (asthmatic patients n=10 and healthy controls n=9) were included. The COVID-19 patients were followed up at about 8 months and 16 months after discharge. The clinical characteristics, lymphocyte subsets, memory T cells, and humoral immunity including SARS-CoV-2 specific antibodies, SARS-CoV-2 pseudotyped virus neutralization assay, and memory B cells were analyzed in these subjects. RESULTS: The strength of virus-specific T cell response in COVID-19 survivors was positively correlated with the percentage of blood eosinophils and Treg cells (r=0.4007, p=0.0188; and r=0.4435, p=0.0086 respectively) at 8-month follow-up. There were no statistical differences in the levels of SARS-CoV-2-specific T cell response between the COVID-19 survivors with, and without, asthma. Compared to those without asthma, the COVID-19 with asthma survivors had higher levels of SARS-CoV-2-specific neutralizing antibodies (NAbs) at the 8-month follow-up (p<0.05). Moreover, the level of NAbs in COVID-19 survivors was positively correlated with the percentage of Treg and cTfh2 cells (r=0.5037, p=0.002; and r=0.4846, p=0.0141), and negatively correlated with the percentage of Th1 and Th17 cells (r=-0.5701, p=0.0003; and r=-0.3656, p=0.0308), the ratio of Th1/Th2, Th17/Treg, and cTfh1/cTfh2 cell (r=-0.5356, r=-0.5947, r=-0.4485; all p<0.05). The decay rate of NAbs in the COVID-19 survivors with asthma was not significantly different from that of those without asthma at 16-month follow-up. CONCLUSION: The level of SARS-CoV-2-specific NAbs in COVID-19 survivors with asthma was higher than that of those without asthma at 8-month follow-up. The SARS-CoV-2-specific T cell immunity was associated with blood eosinophils and Treg percentages. The SARS-CoV-2-specific humoral immunity was closely associated with cTfh2/cTfh1 imbalance and Treg/Th17 ratio. According to the findings, asthmatic patients in COVID-19 convalescent period may benefit from an enhanced specific humoral immunity, which associates with skewed Th2/Th1 and Treg/Th17 immune. Frontiers Media S.A. 2022-07-18 /pmc/articles/PMC9339657/ /pubmed/35924252 http://dx.doi.org/10.3389/fimmu.2022.947724 Text en Copyright © 2022 Chen, Yue, Zhang, Bai, Qin, Zhang, Wu, Li, Xu, Jiang, Yang, Xu, Zhu, Xie and Gong https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Li
Yue, Junqing
Zhang, Shengding
Bai, Wenxue
Qin, Lu
Zhang, Cong
Wu, Bihao
Li, Moxuan
Xu, Shuyun
Jiang, Qing
Yang, Lin
Xu, Qingxiu
Zhu, Rongfei
Xie, Min
Gong, Rui
SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma
title SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma
title_full SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma
title_fullStr SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma
title_full_unstemmed SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma
title_short SARS-CoV-2-Specific Adaptive Immunity in COVID-19 Survivors With Asthma
title_sort sars-cov-2-specific adaptive immunity in covid-19 survivors with asthma
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339657/
https://www.ncbi.nlm.nih.gov/pubmed/35924252
http://dx.doi.org/10.3389/fimmu.2022.947724
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