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

DOI
https://doi.org/10.1002/cti2.1403
Journal volume & issue
Vol. 11, no. 8
pp. n/a – n/a

Abstract

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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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