Dynamic Antibody Response and Hybrid Immunity Following Multiple COVID-19 Vaccine Doses and Infection: A Case Study
This case study highlights the dynamic nature of the antibody response to SARS-CoV-2 in a vulnerable subject aged 70 years between 2021 and 2023. This individual had been vaccinated with six doses of the ancestral (Wuhan-Hu-1) COVID-19 vaccine and had a breakthrough infection 126 days after receivin...
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Published in | Curēus (Palo Alto, CA) Vol. 15; no. 9; p. e45531 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Palo Alto
Springer Nature B.V
19.09.2023
Cureus |
Subjects | |
Online Access | Get full text |
ISSN | 2168-8184 2168-8184 |
DOI | 10.7759/cureus.45531 |
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Abstract | This case study highlights the dynamic nature of the antibody response to SARS-CoV-2 in a vulnerable subject aged 70 years between 2021 and 2023. This individual had been vaccinated with six doses of the ancestral (Wuhan-Hu-1) COVID-19 vaccine and had a breakthrough infection 126 days after receiving Covovax™ (CO) as the sixth dose. The serostatus for total immunoglobulin specific to the receptor binding domain (total RBD Ig) changed from negative to positive following a two-dose CoronaVac (CV) vaccination, indicating a successful immune response. Booster doses, including AZD1222 (AZ), half-dose BNT162b2 (PF), and CO, increased the total RBD Ig levels, except for CV. The individual experienced a breakthrough infection by the Omicron BA.5 variant, leading to a substantial surge in total RBD Ig to over 105 U/mL. This generated sustained and extended antibody persistence, with the half-life of total RBD Ig lasting approximately 103.6 days. Furthermore, it has been observed that this breakthrough infection generated the highest neutralizing antibodies against BA.5, followed by XBB.1.5, BQ.1.1, and BA.2.75, respectively. |
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AbstractList | This case study highlights the dynamic nature of the antibody response to SARS-CoV-2 in a vulnerable subject aged 70 years between 2021 and 2023. This individual had been vaccinated with six doses of the ancestral (Wuhan-Hu-1) COVID-19 vaccine and had a breakthrough infection 126 days after receiving Covovax™ (CO) as the sixth dose. The serostatus for total immunoglobulin specific to the receptor binding domain (total RBD Ig) changed from negative to positive following a two-dose CoronaVac (CV) vaccination, indicating a successful immune response. Booster doses, including AZD1222 (AZ), half-dose BNT162b2 (PF), and CO, increased the total RBD Ig levels, except for CV. The individual experienced a breakthrough infection by the Omicron BA.5 variant, leading to a substantial surge in total RBD Ig to over 105 U/mL. This generated sustained and extended antibody persistence, with the half-life of total RBD Ig lasting approximately 103.6 days. Furthermore, it has been observed that this breakthrough infection generated the highest neutralizing antibodies against BA.5, followed by XBB.1.5, BQ.1.1, and BA.2.75, respectively. This case study highlights the dynamic nature of the antibody response to SARS-CoV-2 in a vulnerable subject aged 70 years between 2021 and 2023. This individual had been vaccinated with six doses of the ancestral (Wuhan-Hu-1) COVID-19 vaccine and had a breakthrough infection 126 days after receiving Covovax™- (CO) as the sixth dose. The serostatus for total immunoglobulin specific to the receptor binding domain (total RBD Ig) changed from negative to positive following a two-dose CoronaVac (CV) vaccination, indicating a successful immune response. Booster doses, including AZD1222 (AZ), half-dose BNT162b2 (PF), and CO, increased the total RBD Ig levels, except for CV. The individual experienced a breakthrough infection by the Omicron BA.5 variant, leading to a substantial surge in total RBD Ig to over 105 U/mL. This generated sustained and extended antibody persistence, with the half-life of total RBD Ig lasting approximately 103.6 days. Furthermore, it has been observed that this breakthrough infection generated the highest neutralizing antibodies against BA.5, followed by XBB.1.5, BQ.1.1, and BA.2.75, respectively.This case study highlights the dynamic nature of the antibody response to SARS-CoV-2 in a vulnerable subject aged 70 years between 2021 and 2023. This individual had been vaccinated with six doses of the ancestral (Wuhan-Hu-1) COVID-19 vaccine and had a breakthrough infection 126 days after receiving Covovax™- (CO) as the sixth dose. The serostatus for total immunoglobulin specific to the receptor binding domain (total RBD Ig) changed from negative to positive following a two-dose CoronaVac (CV) vaccination, indicating a successful immune response. Booster doses, including AZD1222 (AZ), half-dose BNT162b2 (PF), and CO, increased the total RBD Ig levels, except for CV. The individual experienced a breakthrough infection by the Omicron BA.5 variant, leading to a substantial surge in total RBD Ig to over 105 U/mL. This generated sustained and extended antibody persistence, with the half-life of total RBD Ig lasting approximately 103.6 days. Furthermore, it has been observed that this breakthrough infection generated the highest neutralizing antibodies against BA.5, followed by XBB.1.5, BQ.1.1, and BA.2.75, respectively. This case study highlights the dynamic nature of the antibody response to SARS-CoV-2 in a vulnerable subject aged 70 years between 2021 and 2023. This individual had been vaccinated with six doses of the ancestral (Wuhan-Hu-1) COVID-19 vaccine and had a breakthrough infection 126 days after receiving Covovax™ (CO) as the sixth dose. The serostatus for total immunoglobulin specific to the receptor binding domain (total RBD Ig) changed from negative to positive following a two-dose CoronaVac (CV) vaccination, indicating a successful immune response. Booster doses, including AZD1222 (AZ), half-dose BNT162b2 (PF), and CO, increased the total RBD Ig levels, except for CV. The individual experienced a breakthrough infection by the Omicron BA.5 variant, leading to a substantial surge in total RBD Ig to over 10 5 U/mL. This generated sustained and extended antibody persistence, with the half-life of total RBD Ig lasting approximately 103.6 days. Furthermore, it has been observed that this breakthrough infection generated the highest neutralizing antibodies against BA.5, followed by XBB.1.5, BQ.1.1, and BA.2.75, respectively. |
Author | Suntronwong, Nungruthai Wanlapakorn, Nasamon Duangchinda, Thaneeya Poovorawan, Yong Kanokudom, Sitthichai |
AuthorAffiliation | 1 Center of Excellence in Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok, THA 3 Center of Excellence In Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok, THA 2 Molecular Biology of Dengue and Flaviviruses Research Team, National Center for Genetic Engineering and Biotechnology (BIOTEC) National Science and Technology Development Agency, Pathum Thani, THA |
AuthorAffiliation_xml | – name: 3 Center of Excellence In Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok, THA – name: 1 Center of Excellence in Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok, THA – name: 2 Molecular Biology of Dengue and Flaviviruses Research Team, National Center for Genetic Engineering and Biotechnology (BIOTEC) National Science and Technology Development Agency, Pathum Thani, THA |
Author_xml | – sequence: 1 givenname: Sitthichai surname: Kanokudom fullname: Kanokudom, Sitthichai – sequence: 2 givenname: Nungruthai surname: Suntronwong fullname: Suntronwong, Nungruthai – sequence: 3 givenname: Thaneeya surname: Duangchinda fullname: Duangchinda, Thaneeya – sequence: 4 givenname: Nasamon surname: Wanlapakorn fullname: Wanlapakorn, Nasamon – sequence: 5 givenname: Yong surname: Poovorawan fullname: Poovorawan, Yong |
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Cites_doi | 10.1038/s41591-021-01540-1 10.1016/j.cell.2021.12.032 10.1038/s41586-022-04980-y 10.1001/jamanetworkopen.2022.31778 10.1056/NEJMoa2201688 10.1016/j.jinf.2022.04.018 10.1056/NEJMc2202542 10.1126/science.abn4947 10.1080/21645515.2022.2029111 10.3390/vaccines11071184 10.3390/vaccines10010086 10.1038/s41591-022-02138-x 10.1126/science.adc9127 10.1016/j.virusres.2021.198555 10.1172/JCI167955 10.1038/s41467-022-33550-z 10.1038/s41541-021-00369-6 10.1186/s12879-023-08272-2 |
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Copyright | Copyright © 2023, Kanokudom et al. This work is published under https://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Copyright © 2023, Kanokudom et al. Copyright © 2023, Kanokudom et al. 2023 Kanokudom et al. |
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