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. 2021 Aug 27;13(9):1708. doi: 10.3390/v13091708

Table 3.

Proteins and peptides utilized as recall antigens for ELISpot analysis of splenocytes obtained after delivery of MVA vaccines that encoded NP, M2 or M2e. p values were calculated by t-test, 2-tailed, equal variance. Influenza recall antigens were derived from proteins of H1N1 PR8 INFV A.

Statistical
Difference Compared to Medium
Recall Antigen Antigen MHC Class Spots Per 300,000 Cells
Medium None None 3 ± 2
p < 0.001 NP (H1N1) protein NP NA 1 98 ± 56
p < 0.001 TYQRTRALV peptide NP I 325 ± 126
p < 0.001 RLIQNSLTIERMVLS peptide NP II 53 ± 31
None M2 protein (H1N1 PR8) M2 NA 1 11 ± 17
None IAANIIGIL peptide 2 M2 I 7 ± 11
None IYRRFKYGL peptide 2 M2 I 3 ± 2
None LLTEVETPI peptide M2e I 7 ± 11
p < 0.001 VETPIRNEW peptide M2e I 38 ± 18
p < 0.001 SLLTEVETPIRNEWGCRCNGSSD peptide M2e II 26 ± 18
NA 3 SPGAAGWDL and VGPSNSPTF MVA I 666 ± 71

1 Not applicable, recall antigen was whole-molecule protein. 2 Peptides IAANIIGIL and IYRRFKYGL are within the internal domains of the M2 molecule, and are not found within the external M2e domain, therefore were not contained within the vaccines tested. These low and high scoring (respectively) epitope peptides [28] are negative controls. 3 Not applicable. MVA MHC class I peptides [29] were system suitability standards.