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. 2021 May 28;12:635942. doi: 10.3389/fimmu.2021.635942

Table 3.

T cell immune dominance of SARS-CoV-2 proteins.

ID. ∑ SFU ORF3a N Nsp12 Nsp5 S (A & B) S-RBD M
dC1 191 10% 12% 13% 0% 40% 7% 18%
dC2 267 12% 25% 12% 0% 40% 2% 10%
dC3 230 10% 13% 3% 5% 50% 10% 10%
dC4 264 3% 21% 6% 3% 47% 7% 13%
dC5 216 1% 16% 0% 2% 49% 23% 9%
dC6 332 5% 31% 11% 2% 35% 4% 14%
dC7 253 12% 10% 9% 1% 51% 3% 15%
dC8 184 6% 21% 17% 1% 31% 16% 7%
dC9 81 0% 19% 0% 0% 24% 8% 49%
x¯ na 6% 18% 8% 2% 40% 9% 16%
σ na 4% 6% 6% 3% 9% 6% 12%
# Pept. na 66 102 231 74 315 53 53
x¯/(# Pept.) na 0.09% 0.18% 0.03% 0.03% 0.13% 0.17% 0.30%

The total SARS-CoV-2-specific T cell mass (∑SFU) was calculated by adding up for each SARS-CoV-2-recovered donor the numbers of SFU elicited by all SARS-CoV-2 peptide pools in that donor at 1.5 µg/mL (see the raw data in Supplementary Table 5 ). In the top panel, the percentage of T cells targeting each of the SARS-CoV-2 antigens is shown relative to the total clonal SARS-CoV-2-specific T cell mass in that individual, representing an immune dominance index. The superimposed heatmap specifies the affinity level of the respective T cell population, with the color code defined in Table 2 . The lower panel shows the mean percentage (x¯) and SD of this immunodominance index for the cohort. Addressing the hypothesis that T cell immune dominance of a SARS-CoV-2 antigen is related to its size, the number of peptides in each pool is shown (# Pept.) and the mean immune dominance index ( x¯ ) is normalized for the number of peptides ( x¯ /(# Pept).