Please use this identifier to cite or link to this item: https://doi.org/10.1002/cti2.1403
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dc.titleHeterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine
dc.contributor.authorGoh, Yun Shan
dc.contributor.authorFong, Siew-Wai
dc.contributor.authorRouers, Angeline
dc.contributor.authorChang, Zi Wei
dc.contributor.authorTay, Matthew Zirui
dc.contributor.authorChavatte, Jean-Marc
dc.contributor.authorZhuo, Nicole Ziyi
dc.contributor.authorHor, Pei Xiang
dc.contributor.authorLoh, Chiew Yee
dc.contributor.authorHuang, Yuling
dc.contributor.authorWong, Joel Xu En
dc.contributor.authorTan, Yong Jie
dc.contributor.authorLim, Daniel Rui Xiang
dc.contributor.authorWang, Bei
dc.contributor.authorNgoh, Eve Zi Xian
dc.contributor.authorSalleh, Siti Nazihah Mohd
dc.contributor.authorLee, Raphael Tze Chuen
dc.contributor.authorPada, Surinder
dc.contributor.authorSun, Louisa Jin
dc.contributor.authorOng, Desmond Luan Seng
dc.contributor.authorSomani, Jyoti
dc.contributor.authorLee, Eng Sing
dc.contributor.authorMaurer-Stroh, Sebastian
dc.contributor.authorWang, Cheng-I
dc.contributor.authorLeo, Yee-Sin
dc.contributor.authorLin, Raymond TP
dc.contributor.authorRen, Ee Chee
dc.contributor.authorLye, David C
dc.contributor.authorYoung, Barnaby Edward
dc.contributor.authorLim, Poh Lian
dc.contributor.authorNg, Lisa FP
dc.contributor.authorRenia, Laurent
dc.date.accessioned2022-11-21T09:18:39Z
dc.date.available2022-11-21T09:18:39Z
dc.date.issued2022-01-01
dc.identifier.citationGoh, 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 (2022-01-01). Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine. CLINICAL & TRANSLATIONAL IMMUNOLOGY 11 (8). ScholarBank@NUS Repository. https://doi.org/10.1002/cti2.1403
dc.identifier.issn2050-0068
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/234734
dc.description.abstractObjective: 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.
dc.language.isoen
dc.publisherWILEY
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectImmunology
dc.subjectAllergic
dc.subjectAntibodies
dc.subjectB cells
dc.subjectCoronaVac
dc.subjectCOVID-19
dc.subjectDelta
dc.subjectOmicron
dc.subjectS protein
dc.subjectSARS-CoV-2
dc.subjectT cells
dc.subjectBNT162B2
dc.subjectIMMUNOGENICITY
dc.typeArticle
dc.date.updated2022-11-19T06:37:27Z
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.contributor.departmentSURGERY
dc.contributor.departmentORTHOPAEDIC SURGERY
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.contributor.departmentDEAN'S OFFICE (SSH SCH OF PUBLIC HEALTH)
dc.contributor.departmentMEDICINE
dc.description.doi10.1002/cti2.1403
dc.description.sourcetitleCLINICAL & TRANSLATIONAL IMMUNOLOGY
dc.description.volume11
dc.description.issue8
dc.published.statePublished
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