<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Goh YS</submitter><funding>Agency for Science, Technology and Research</funding><pagination>e1403</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9398778</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(8)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>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.&lt;h4>Methods&lt;/h4>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 </pubmed_abstract><journal>Clinical &amp; translational immunology</journal><pubmed_title>Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine.</pubmed_title><pmcid>PMC9398778</pmcid><funding_grant_id>H/20/04/g1/006</funding_grant_id><funding_grant_id>ACCL/19‐GAP064‐R20H‐H</funding_grant_id><pubmed_authors>Lye DC</pubmed_authors><pubmed_authors>Wong JXE</pubmed_authors><pubmed_authors>Wang CI</pubmed_authors><pubmed_authors>Salleh SNM</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Lim PL</pubmed_authors><pubmed_authors>Zhuo NZ</pubmed_authors><pubmed_authors>Pada S</pubmed_authors><pubmed_authors>NCID Study Group</pubmed_authors><pubmed_authors>Lim DRX</pubmed_authors><pubmed_authors>Ren EC</pubmed_authors><pubmed_authors>Ong DLS</pubmed_authors><pubmed_authors>Lee ES</pubmed_authors><pubmed_authors>Rouers A</pubmed_authors><pubmed_authors>Ng LF</pubmed_authors><pubmed_authors>Lee RTC</pubmed_authors><pubmed_authors>Tay MZ</pubmed_authors><pubmed_authors>Ngoh EZX</pubmed_authors><pubmed_authors>Renia L</pubmed_authors><pubmed_authors>Somani J</pubmed_authors><pubmed_authors>Young BE</pubmed_authors><pubmed_authors>Chavatte JM</pubmed_authors><pubmed_authors>Loh CY</pubmed_authors><pubmed_authors>Goh YS</pubmed_authors><pubmed_authors>Hor PX</pubmed_authors><pubmed_authors>Tan YJ</pubmed_authors><pubmed_authors>Chang ZW</pubmed_authors><pubmed_authors>COVID‐19 Study Group</pubmed_authors><pubmed_authors>Maurer-Stroh S</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Leo YS</pubmed_authors><pubmed_authors>Sun LJ</pubmed_authors><pubmed_authors>Fong SW</pubmed_authors><pubmed_authors>Lin RT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heterologous booster vaccination with CoronaVac following prime vaccination with mRNA vaccine.</name><description>&lt;h4>Objective&lt;/h4>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.&lt;h4>Methods&lt;/h4>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 </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-26T19:43:21.825Z</modification><creation>2024-11-14T03:43:51.006Z</creation></dates><accession>S-EPMC9398778</accession><cross_references><pubmed>36016852</pubmed><doi>10.1002/cti2.1403</doi></cross_references></HashMap>