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Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization

BACKGROUND: The immunogenicity of booster inactivated COVID‐19 vaccines in patients with type 2 diabetes mellitus (T2DM) has remained unclear. Our study aims to investigate the antibody response to inactivated COVID‐19 vaccine following booster vaccination in patients with T2DM. METHODS: A total of...

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Autores principales: Li, Haolong, Wang, Yao, Li, Xiaomeng, Wang, Siyu, Feng, Xinxin, Xiao, Xinhua, Li, Yongzhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667667/
https://www.ncbi.nlm.nih.gov/pubmed/37518861
http://dx.doi.org/10.1111/1753-0407.13448
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author Li, Haolong
Wang, Yao
Li, Xiaomeng
Wang, Siyu
Feng, Xinxin
Xiao, Xinhua
Li, Yongzhe
author_facet Li, Haolong
Wang, Yao
Li, Xiaomeng
Wang, Siyu
Feng, Xinxin
Xiao, Xinhua
Li, Yongzhe
author_sort Li, Haolong
collection PubMed
description BACKGROUND: The immunogenicity of booster inactivated COVID‐19 vaccines in patients with type 2 diabetes mellitus (T2DM) has remained unclear. Our study aims to investigate the antibody response to inactivated COVID‐19 vaccine following booster vaccination in patients with T2DM. METHODS: A total of 201 patients with T2DM and 102 healthy controls (HCs) were enrolled. The levels of anti‐SARS‐CoV‐2 total antibodies, anti‐receptor‐binding domain (RBD)‐specific IgG, neutralizing antibody (NAb) toward SARS‐CoV‐2 wild type (WT), and NAb toward SARS‐CoV‐2 Omicron BA.4/5 subvariant were measured to evaluate the vaccine‐induced immunological responses. RESULTS: The titers of anti‐RBD‐specific IgG (p = 0.018) and inhibition rates of NAb toward WT (p = 0.007) were significantly decreased in patients with T2DM compared to HCs after booster vaccination for more than 6 months. Both HCs and patients with T2DM showed poor resistance against BA.4/5 due to the detected inhibition rates being lower than the positive threshold. The levels of anti‐RBD‐specific IgG were positively associated with the proportions of CD3(+)CD4(−)CD8(−) T cells (p = 0.045), and patients with T2DM who had anti‐RBD‐specific IgG positivity showed higher proportions of CD3(+)CD4(−)CD8(−) T cells compared to those negative (p = 0.005). CONCLUSIONS: Patients with T2DM showed impaired antibody responses after booster vaccination for more than 6 months. Decreased anti‐BA.4/5 responses give rise to the possibility of breakthrough infections for both patients with T2DM and HCs.
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spelling pubmed-106676672023-07-30 Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization Li, Haolong Wang, Yao Li, Xiaomeng Wang, Siyu Feng, Xinxin Xiao, Xinhua Li, Yongzhe J Diabetes Editor's Recommendations BACKGROUND: The immunogenicity of booster inactivated COVID‐19 vaccines in patients with type 2 diabetes mellitus (T2DM) has remained unclear. Our study aims to investigate the antibody response to inactivated COVID‐19 vaccine following booster vaccination in patients with T2DM. METHODS: A total of 201 patients with T2DM and 102 healthy controls (HCs) were enrolled. The levels of anti‐SARS‐CoV‐2 total antibodies, anti‐receptor‐binding domain (RBD)‐specific IgG, neutralizing antibody (NAb) toward SARS‐CoV‐2 wild type (WT), and NAb toward SARS‐CoV‐2 Omicron BA.4/5 subvariant were measured to evaluate the vaccine‐induced immunological responses. RESULTS: The titers of anti‐RBD‐specific IgG (p = 0.018) and inhibition rates of NAb toward WT (p = 0.007) were significantly decreased in patients with T2DM compared to HCs after booster vaccination for more than 6 months. Both HCs and patients with T2DM showed poor resistance against BA.4/5 due to the detected inhibition rates being lower than the positive threshold. The levels of anti‐RBD‐specific IgG were positively associated with the proportions of CD3(+)CD4(−)CD8(−) T cells (p = 0.045), and patients with T2DM who had anti‐RBD‐specific IgG positivity showed higher proportions of CD3(+)CD4(−)CD8(−) T cells compared to those negative (p = 0.005). CONCLUSIONS: Patients with T2DM showed impaired antibody responses after booster vaccination for more than 6 months. Decreased anti‐BA.4/5 responses give rise to the possibility of breakthrough infections for both patients with T2DM and HCs. Wiley Publishing Asia Pty Ltd 2023-07-30 /pmc/articles/PMC10667667/ /pubmed/37518861 http://dx.doi.org/10.1111/1753-0407.13448 Text en © 2023 The Authors. Journal of Diabetes published by Ruijin Hospital, Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Editor's Recommendations
Li, Haolong
Wang, Yao
Li, Xiaomeng
Wang, Siyu
Feng, Xinxin
Xiao, Xinhua
Li, Yongzhe
Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization
title Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization
title_full Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization
title_fullStr Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization
title_full_unstemmed Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization
title_short Antibody response to inactivated COVID‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization
title_sort antibody response to inactivated covid‐19 vaccine in patients with type 2 diabetes mellitus after the booster immunization
topic Editor's Recommendations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667667/
https://www.ncbi.nlm.nih.gov/pubmed/37518861
http://dx.doi.org/10.1111/1753-0407.13448
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