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. 2023 Mar 13;3(4):418–435. doi: 10.1038/s43587-023-00379-0

Fig. 4. Comparison of SARS-CoV-2 epitope-specific CD8 T cells between young and old vaccine recipients.

Fig. 4

a, Representative data for in vitro detection of epitope-specific CD8 T cells in the HLA-A2+ healthy donors before and after second doses (7 days and 50 days) of inactivated SARS-CoV-2 vaccine with tetramers prepared using SARS-CoV-2 epitopes. Variant strain IDs are the same as listed in Fig. 2a. Cells were stimulated for 16 hours before tetramer staining. The flow cytometry gating strategy is shown in Extended Data Fig. 4a. b, Comparison of epitope-specific CD8 T cells between HLA-A2+ healthy young and old donors, 7 days (top row) and 50 days (bottom row) after second doses of inactivated SARS-CoV-2 vaccine. Specific CD8 T cells were stained with tetramers prepared using ancestral and mutant SARS-CoV-2 epitope individually after 16-hour stimulation. Paired ancestral and mutant epitopes are listed adjacently on the x axis. Data are shown as mean ± s.d. n = 5 for S 269–277 and S P272L; otherwise, n = 45 in all the other tests for both the young and old groups. ****P < 0.0001, ***P < 0.001, **P < 0.01, *P < 0.05 and NS, not statistically significant (P ≥ 0.05), two-sided t-test. c, Overall statistics and comparison of SARS-CoV-2 epitope-specific CD8 T cells on the 7th and 50th days after the second dose in young and old recipients. d, Summary statistics of detection fold change of CD8 T cells specific to SARS-CoV-2 epitopes between 7 days and 50 days after the second dose. Data shown are mean ± s.d., n = 45 for both the young and old groups.