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Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine
OBJECTIVE: Despite the high vaccine efficacy of mRNA COVID‐19 vaccines, there are individuals who developed excessive reactogenic and/or allergic responses after the first mRNA dose and were considered ineligible for further mRNA doses. CoronaVac, an inactivated SARS‐CoV‐2 vaccine, is recommended in...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9398778/ https://www.ncbi.nlm.nih.gov/pubmed/36016852 http://dx.doi.org/10.1002/cti2.1403 |
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author | Goh, Yun Shan Fong, Siew‐Wai Rouers, Angeline Chang, Zi Wei Tay, Matthew Zirui Chavatte, Jean‐Marc Zhuo, Nicole Ziyi Hor, Pei Xiang Loh, Chiew Yee Huang, Yuling Wong, Joel Xu En Tan, Yong Jie Lim, Daniel Rui Xiang Wang, Bei Ngoh, Eve Zi Xian Salleh, Siti Nazihah Mohd Lee, Raphael Tze Chuen Pada, Surinder Sun, Louisa Jin Ong, Desmond Luan Seng Somani, Jyoti Lee, Eng Sing Maurer‐Stroh, Sebastian Wang, Cheng‐I Leo, Yee‐Sin Lin, Raymond TP Ren, Ee Chee Lye, David C Young, Barnaby Edward Lim, Poh Lian Ng, Lisa FP Renia, Laurent |
author_facet | Goh, Yun Shan Fong, Siew‐Wai Rouers, Angeline Chang, Zi Wei Tay, Matthew Zirui Chavatte, Jean‐Marc Zhuo, Nicole Ziyi Hor, Pei Xiang Loh, Chiew Yee Huang, Yuling Wong, Joel Xu En Tan, Yong Jie Lim, Daniel Rui Xiang Wang, Bei Ngoh, Eve Zi Xian Salleh, Siti Nazihah Mohd Lee, Raphael Tze Chuen Pada, Surinder Sun, Louisa Jin Ong, Desmond Luan Seng Somani, Jyoti Lee, Eng Sing Maurer‐Stroh, Sebastian Wang, Cheng‐I Leo, Yee‐Sin Lin, Raymond TP Ren, Ee Chee Lye, David C Young, Barnaby Edward Lim, Poh Lian Ng, Lisa FP Renia, Laurent |
author_sort | Goh, Yun Shan |
collection | PubMed |
description | OBJECTIVE: Despite the high vaccine efficacy of mRNA COVID‐19 vaccines, there are individuals who developed excessive reactogenic and/or allergic responses after the first mRNA dose and were considered ineligible for further mRNA doses. CoronaVac, an inactivated SARS‐CoV‐2 vaccine, is recommended in Singapore as an alternative. METHODS: Individuals, ineligible for further mRNA vaccines (BNT162b2 or mRNA‐1273) because of excessive reactive responses to prime mRNA vaccination, were recruited and offered two doses of CoronaVac as booster vaccination 38–224 days post their mRNA vaccine dose. Individuals who did not develop any excessive reactive responses after the prime mRNA vaccination were also recruited and given another mRNA vaccine as booster vaccination. Blood samples were collected at days 0, 21 and 90 post first CoronaVac dose and mRNA dose, respectively, for analysis. RESULTS: We showed that two CoronaVac booster doses induced specific immunity in these mRNA vaccine‐primed individuals. Although the spike‐specific antibody response was lower, their memory B cell response against the receptor‐binding domain (RBD) of the spike protein was similar, compared with individuals who received two BNT162b2 injections. The spike‐specific memory T cell response also increased following CoronaVac booster doses. However, specific immunity against the Omicron variant was low, similar to individuals with two BNT162b2 doses. CONCLUSION: Our findings showed that while mRNA vaccine‐primed individuals can opt for two subsequent doses of CoronaVac, an additional dose may be necessary to achieve protection, especially against newly emerging immune escape variants such as Omicron. |
format | Online Article Text |
id | pubmed-9398778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93987782022-08-24 Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine Goh, Yun Shan Fong, Siew‐Wai Rouers, Angeline Chang, Zi Wei Tay, Matthew Zirui Chavatte, Jean‐Marc Zhuo, Nicole Ziyi Hor, Pei Xiang Loh, Chiew Yee Huang, Yuling Wong, Joel Xu En Tan, Yong Jie Lim, Daniel Rui Xiang Wang, Bei Ngoh, Eve Zi Xian Salleh, Siti Nazihah Mohd Lee, Raphael Tze Chuen Pada, Surinder Sun, Louisa Jin Ong, Desmond Luan Seng Somani, Jyoti Lee, Eng Sing Maurer‐Stroh, Sebastian Wang, Cheng‐I Leo, Yee‐Sin Lin, Raymond TP Ren, Ee Chee Lye, David C Young, Barnaby Edward Lim, Poh Lian Ng, Lisa FP Renia, Laurent Clin Transl Immunology Original Articles OBJECTIVE: Despite the high vaccine efficacy of mRNA COVID‐19 vaccines, there are individuals who developed excessive reactogenic and/or allergic responses after the first mRNA dose and were considered ineligible for further mRNA doses. CoronaVac, an inactivated SARS‐CoV‐2 vaccine, is recommended in Singapore as an alternative. METHODS: Individuals, ineligible for further mRNA vaccines (BNT162b2 or mRNA‐1273) because of excessive reactive responses to prime mRNA vaccination, were recruited and offered two doses of CoronaVac as booster vaccination 38–224 days post their mRNA vaccine dose. Individuals who did not develop any excessive reactive responses after the prime mRNA vaccination were also recruited and given another mRNA vaccine as booster vaccination. Blood samples were collected at days 0, 21 and 90 post first CoronaVac dose and mRNA dose, respectively, for analysis. RESULTS: We showed that two CoronaVac booster doses induced specific immunity in these mRNA vaccine‐primed individuals. Although the spike‐specific antibody response was lower, their memory B cell response against the receptor‐binding domain (RBD) of the spike protein was similar, compared with individuals who received two BNT162b2 injections. The spike‐specific memory T cell response also increased following CoronaVac booster doses. However, specific immunity against the Omicron variant was low, similar to individuals with two BNT162b2 doses. CONCLUSION: Our findings showed that while mRNA vaccine‐primed individuals can opt for two subsequent doses of CoronaVac, an additional dose may be necessary to achieve protection, especially against newly emerging immune escape variants such as Omicron. John Wiley and Sons Inc. 2022-08-23 /pmc/articles/PMC9398778/ /pubmed/36016852 http://dx.doi.org/10.1002/cti2.1403 Text en © 2022 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Goh, Yun Shan Fong, Siew‐Wai Rouers, Angeline Chang, Zi Wei Tay, Matthew Zirui Chavatte, Jean‐Marc Zhuo, Nicole Ziyi Hor, Pei Xiang Loh, Chiew Yee Huang, Yuling Wong, Joel Xu En Tan, Yong Jie Lim, Daniel Rui Xiang Wang, Bei Ngoh, Eve Zi Xian Salleh, Siti Nazihah Mohd Lee, Raphael Tze Chuen Pada, Surinder Sun, Louisa Jin Ong, Desmond Luan Seng Somani, Jyoti Lee, Eng Sing Maurer‐Stroh, Sebastian Wang, Cheng‐I Leo, Yee‐Sin Lin, Raymond TP Ren, Ee Chee Lye, David C Young, Barnaby Edward Lim, Poh Lian Ng, Lisa FP Renia, Laurent Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine |
title | Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine |
title_full | Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine |
title_fullStr | Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine |
title_full_unstemmed | Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine |
title_short | Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine |
title_sort | heterologous booster vaccination with coronavac following prime vaccination with mrna vaccine |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9398778/ https://www.ncbi.nlm.nih.gov/pubmed/36016852 http://dx.doi.org/10.1002/cti2.1403 |
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