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Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients

BACKGROUND: A third mRNA vaccine booster is recommended to improve immunity against SARS-CoV-2 in kidney transplant recipients (KTRs). However, the immunity against SARS-CoV-2 Ancestral strain and Delta and Omicron variants elicited by the third dose of inactivated booster vaccine in KTRs remains un...

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Autores principales: Zhang, Lei, Yang, Jiaqing, Lai, Changchun, Wan, Li, Xiong, Shilong, Kong, Weiya, Liu, Zijian, Yu, Pei, Chen, Mingxiao, Mai, Weikang, Khan, Shahzad Akbar, Deng, Min, Chen, Lu, Lei, Yu, Zhou, Qiang, Yu, Nan, Li, Pingchao, Chen, Zheng, Ji, Tianxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868555/
https://www.ncbi.nlm.nih.gov/pubmed/36700230
http://dx.doi.org/10.3389/fimmu.2022.1042784
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author Zhang, Lei
Yang, Jiaqing
Lai, Changchun
Wan, Li
Xiong, Shilong
Kong, Weiya
Liu, Zijian
Yu, Pei
Chen, Mingxiao
Mai, Weikang
Khan, Shahzad Akbar
Deng, Min
Chen, Lu
Lei, Yu
Zhou, Qiang
Yu, Nan
Li, Pingchao
Chen, Zheng
Ji, Tianxing
author_facet Zhang, Lei
Yang, Jiaqing
Lai, Changchun
Wan, Li
Xiong, Shilong
Kong, Weiya
Liu, Zijian
Yu, Pei
Chen, Mingxiao
Mai, Weikang
Khan, Shahzad Akbar
Deng, Min
Chen, Lu
Lei, Yu
Zhou, Qiang
Yu, Nan
Li, Pingchao
Chen, Zheng
Ji, Tianxing
author_sort Zhang, Lei
collection PubMed
description BACKGROUND: A third mRNA vaccine booster is recommended to improve immunity against SARS-CoV-2 in kidney transplant recipients (KTRs). However, the immunity against SARS-CoV-2 Ancestral strain and Delta and Omicron variants elicited by the third dose of inactivated booster vaccine in KTRs remains unknown. METHODS: The blood parameters related to blood cells count, hepatic function, kidney function, heart injury and immunity were explored clinically from laboratory examinations. SARS-CoV-2 specific antibody IgG titer was detected using an enzyme-linked immunosorbent assay. Cellular immunity was analyzed using interferon-γ enzyme-linked immunospot assay. RESULTS: The results showed that there were no severe adverse effects and apparent changes of clinical laboratory biomarkers in KTRs and healthy volunteers (HVs) after homologous inactivated vaccine booster. A third dose of inactivated vaccine booster significantly increased anti-Ancestral-spike-trimer-IgG and anti-Ancestral-receptor binding domain (RBD)-IgG titers in KTRs and HVs compared with the second vaccination. However, the anti-Delta-RBD-IgG and anti-Omicron-RBD-IgG titers were significantly lower than anti-Ancestral-RBD-IgG titer in KTRs and HVs after the third dose. Notably, only 25.6% (10/39) and 10.3% (4/39) of KTRs had seropositivity for anti-Delta-RBD-IgG and anti-Omicron-RBD-IgG after booster, which were significantly lower than HVs (anti-Delta-RBD-IgG: 100%, anti-Omicron-RBD-IgG: 77.8%). Ancestral strain nucleocapsid protein and spike specific T cell frequency after booster was not significantly increased in KTRs compared with the second dose, significantly lower than that in HVs. Moreover, 33.3% (12/36), 14.3% (3/21) and 14.3% (3/21) of KTRs were positive for the Ancestral strain and Delta and Omicron spike-specific T cells, which were significantly lower than HVs (Ancestral: 80.8%, Delta: 53.8%, and Omicron: 57.7%). CONCLUSIONS: A third dose of inactivated booster vaccine may significantly increase humoral immunity against the Ancestral strain in KTRs, while humoral and cellular immunity against the Delta and Omicron variants were still poor in KTRs.
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spelling pubmed-98685552023-01-24 Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients Zhang, Lei Yang, Jiaqing Lai, Changchun Wan, Li Xiong, Shilong Kong, Weiya Liu, Zijian Yu, Pei Chen, Mingxiao Mai, Weikang Khan, Shahzad Akbar Deng, Min Chen, Lu Lei, Yu Zhou, Qiang Yu, Nan Li, Pingchao Chen, Zheng Ji, Tianxing Front Immunol Immunology BACKGROUND: A third mRNA vaccine booster is recommended to improve immunity against SARS-CoV-2 in kidney transplant recipients (KTRs). However, the immunity against SARS-CoV-2 Ancestral strain and Delta and Omicron variants elicited by the third dose of inactivated booster vaccine in KTRs remains unknown. METHODS: The blood parameters related to blood cells count, hepatic function, kidney function, heart injury and immunity were explored clinically from laboratory examinations. SARS-CoV-2 specific antibody IgG titer was detected using an enzyme-linked immunosorbent assay. Cellular immunity was analyzed using interferon-γ enzyme-linked immunospot assay. RESULTS: The results showed that there were no severe adverse effects and apparent changes of clinical laboratory biomarkers in KTRs and healthy volunteers (HVs) after homologous inactivated vaccine booster. A third dose of inactivated vaccine booster significantly increased anti-Ancestral-spike-trimer-IgG and anti-Ancestral-receptor binding domain (RBD)-IgG titers in KTRs and HVs compared with the second vaccination. However, the anti-Delta-RBD-IgG and anti-Omicron-RBD-IgG titers were significantly lower than anti-Ancestral-RBD-IgG titer in KTRs and HVs after the third dose. Notably, only 25.6% (10/39) and 10.3% (4/39) of KTRs had seropositivity for anti-Delta-RBD-IgG and anti-Omicron-RBD-IgG after booster, which were significantly lower than HVs (anti-Delta-RBD-IgG: 100%, anti-Omicron-RBD-IgG: 77.8%). Ancestral strain nucleocapsid protein and spike specific T cell frequency after booster was not significantly increased in KTRs compared with the second dose, significantly lower than that in HVs. Moreover, 33.3% (12/36), 14.3% (3/21) and 14.3% (3/21) of KTRs were positive for the Ancestral strain and Delta and Omicron spike-specific T cells, which were significantly lower than HVs (Ancestral: 80.8%, Delta: 53.8%, and Omicron: 57.7%). CONCLUSIONS: A third dose of inactivated booster vaccine may significantly increase humoral immunity against the Ancestral strain in KTRs, while humoral and cellular immunity against the Delta and Omicron variants were still poor in KTRs. Frontiers Media S.A. 2023-01-09 /pmc/articles/PMC9868555/ /pubmed/36700230 http://dx.doi.org/10.3389/fimmu.2022.1042784 Text en Copyright © 2023 Zhang, Yang, Lai, Wan, Xiong, Kong, Liu, Yu, Chen, Mai, Khan, Deng, Chen, Lei, Zhou, Yu, Li, Chen and Ji 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
Zhang, Lei
Yang, Jiaqing
Lai, Changchun
Wan, Li
Xiong, Shilong
Kong, Weiya
Liu, Zijian
Yu, Pei
Chen, Mingxiao
Mai, Weikang
Khan, Shahzad Akbar
Deng, Min
Chen, Lu
Lei, Yu
Zhou, Qiang
Yu, Nan
Li, Pingchao
Chen, Zheng
Ji, Tianxing
Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients
title Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients
title_full Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients
title_fullStr Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients
title_full_unstemmed Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients
title_short Immunity against Delta and Omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients
title_sort immunity against delta and omicron variants elicited by homologous inactivated vaccine booster in kidney transplant recipients
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868555/
https://www.ncbi.nlm.nih.gov/pubmed/36700230
http://dx.doi.org/10.3389/fimmu.2022.1042784
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