Design and generation of mRNAs encoding conserved regions of SARS-CoV-2 ORF1ab for T cell-mediated immune activation: supplementary materials

Aim: To generate mRNAs encoding conserved regions within SARS-CoV-2 ORF1ab which can induce strong

T-cell responses to overcome the immune invasion of newly emergent variants. Methods:We selected two

conserved regions with a high density of T-cell epitopes using immunoinformatics for mRNA synthesis. The

ability of testing mRNAs to activate T cells for IFN-γ production was examined by an ELISpot assay and

flow cytometry. Results: Two synthesized mRNAs were successfully translated in MDA-MB-231 cells and

had comparable potency to the spike mRNA to induce CD4+ and CD8+ T-cell responses in PBMCs in 29 out

of 34 participants. Conclusion: This study provides a proof-of-concept for the use of SARS-CoV-2 conserved

regions to develop booster vaccines capable of eliciting T-cell-mediated immunity.