Clinical & Translational Immunology (Jan 2022)
Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine
- Yun Shan Goh,
- Siew‐Wai Fong,
- Angeline Rouers,
- Zi Wei Chang,
- Matthew Zirui Tay,
- Jean‐Marc Chavatte,
- Nicole Ziyi Zhuo,
- Pei Xiang Hor,
- Chiew Yee Loh,
- Yuling Huang,
- Joel Xu En Wong,
- Yong Jie Tan,
- Daniel Rui Xiang Lim,
- Bei Wang,
- Eve Zi Xian Ngoh,
- Siti Nazihah Mohd Salleh,
- Raphael Tze Chuen Lee,
- Surinder Pada,
- Louisa Jin Sun,
- Desmond Luan Seng Ong,
- Jyoti Somani,
- Eng Sing Lee,
- NCID Study Group,
- COVID‐19 Study Group,
- Sebastian Maurer‐Stroh,
- Cheng‐I Wang,
- Yee‐Sin Leo,
- Raymond TP Lin,
- Ee Chee Ren,
- David C Lye,
- Barnaby Edward Young,
- Poh Lian Lim,
- Lisa FP Ng,
- Laurent Renia
Affiliations
- Yun Shan Goh
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Siew‐Wai Fong
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Angeline Rouers
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Zi Wei Chang
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Matthew Zirui Tay
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Jean‐Marc Chavatte
- National Public Health Laboratory National Centre for Infectious Diseases Singapore City Singapore
- Nicole Ziyi Zhuo
- Singapore Immunology Network, Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Pei Xiang Hor
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Chiew Yee Loh
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Yuling Huang
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Joel Xu En Wong
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Yong Jie Tan
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Daniel Rui Xiang Lim
- National Public Health Laboratory National Centre for Infectious Diseases Singapore City Singapore
- Bei Wang
- Singapore Immunology Network, Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Eve Zi Xian Ngoh
- Singapore Immunology Network, Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Siti Nazihah Mohd Salleh
- Singapore Immunology Network, Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Raphael Tze Chuen Lee
- Bioinformatics Institute, A*STAR Singapore City Singapore
- Surinder Pada
- Ng Teng Fong General Hospital Singapore City Singapore
- Louisa Jin Sun
- Infectious Diseases Alexandra Hospital Singapore City Singapore
- Desmond Luan Seng Ong
- National University Polyclinic Singapore City Singapore
- Jyoti Somani
- Division of Infectious Diseases, Department of Medicine, National University Hospital National University Health System Singapore City Singapore
- Eng Sing Lee
- National Healthcare Group Polyclinics Singapore City Singapore
- NCID Study Group
- National Centre for Infectious Diseases (NCID) Singapore City Singapore
- COVID‐19 Study Group
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Sebastian Maurer‐Stroh
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Cheng‐I Wang
- Singapore Immunology Network, Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Yee‐Sin Leo
- Lee Kong Chian School of Medicine Nanyang Technological University Singapore City Singapore
- Raymond TP Lin
- National Public Health Laboratory National Centre for Infectious Diseases Singapore City Singapore
- Ee Chee Ren
- Singapore Immunology Network, Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- David C Lye
- Lee Kong Chian School of Medicine Nanyang Technological University Singapore City Singapore
- Barnaby Edward Young
- Lee Kong Chian School of Medicine Nanyang Technological University Singapore City Singapore
- Poh Lian Lim
- Lee Kong Chian School of Medicine Nanyang Technological University Singapore City Singapore
- Lisa FP Ng
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- Laurent Renia
- A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science Technology and Research (A*STAR) Singapore City Singapore
- DOI
- https://doi.org/10.1002/cti2.1403
- Journal volume & issue
-
Vol. 11,
no. 8
pp. n/a – n/a
Abstract
Abstract 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.
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