Figures & data
Table 1. Age and sex of QIV and ATIV cohorts.
Figure 1. Baseline antibody levels. In (A) individual profiles of HAI antibody responses at day 0 against Wt H1 and modified viruses H1-ΔSb, H1-ΔSa, H1-ΔCb and H1-ΔCa1 and H1-ΔCa2 is represented. GMT value is marked in each column. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (B) SPR before vaccination was calculated as the percentage of patients that achieved HAI titres ≥ 1/40 for each virus and compared to the respective Wt H1 for each cohort. The two-tailed P-value was calculated with the McNemar’s test with the continuity correction; *P < .05, **P < .01, ***P < .001, ****P < .0001.
![Figure 1. Baseline antibody levels. In (A) individual profiles of HAI antibody responses at day 0 against Wt H1 and modified viruses H1-ΔSb, H1-ΔSa, H1-ΔCb and H1-ΔCa1 and H1-ΔCa2 is represented. GMT value is marked in each column. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (B) SPR before vaccination was calculated as the percentage of patients that achieved HAI titres ≥ 1/40 for each virus and compared to the respective Wt H1 for each cohort. The two-tailed P-value was calculated with the McNemar’s test with the continuity correction; *P < .05, **P < .01, ***P < .001, ****P < .0001.](/cms/asset/60fa9c9c-cc9c-455c-9e76-8f74262fe155/temi_a_2135460_f0001_oc.jpg)
Figure 2. Response to vaccination. In (A) individual profiles of HAI antibody responses at day 28 against Wt H1 and modified viruses H1-ΔSb, H1-ΔSa, H1-ΔCb and H1-ΔCa1 and H1-ΔCa2 is represented. GMT value is marked in each column. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (B) SPR after vaccination was calculated as the percentage of patients that achieved HAI titres ≥ 1/40 for each virus and compared to the respective Wt H1 for each cohort. The two-tailed P-value was calculated with the McNemar’s test with the continuity correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (C) Fold induction of HAI titres or GMT increase (calculated as “GMTpost/GMTpre”) is represented of modified viruses H1-ΔSb, H1-ΔSa, H1-ΔCb and H1-ΔCa1 and H1-ΔCa2 compared to the Wt H1 in each cohort. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (D) SCR was calculated as percentage of patients who reached a four-fold-induction for each virus and compared to its respective Wt H1 for each cohort. The two-tailed P-value was calculated with the McNemar’s test with the continuity correction; *P < .05, **P < .01, ***P < .001, ****P < .0001.
![Figure 2. Response to vaccination. In (A) individual profiles of HAI antibody responses at day 28 against Wt H1 and modified viruses H1-ΔSb, H1-ΔSa, H1-ΔCb and H1-ΔCa1 and H1-ΔCa2 is represented. GMT value is marked in each column. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (B) SPR after vaccination was calculated as the percentage of patients that achieved HAI titres ≥ 1/40 for each virus and compared to the respective Wt H1 for each cohort. The two-tailed P-value was calculated with the McNemar’s test with the continuity correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (C) Fold induction of HAI titres or GMT increase (calculated as “GMTpost/GMTpre”) is represented of modified viruses H1-ΔSb, H1-ΔSa, H1-ΔCb and H1-ΔCa1 and H1-ΔCa2 compared to the Wt H1 in each cohort. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (D) SCR was calculated as percentage of patients who reached a four-fold-induction for each virus and compared to its respective Wt H1 for each cohort. The two-tailed P-value was calculated with the McNemar’s test with the continuity correction; *P < .05, **P < .01, ***P < .001, ****P < .0001.](/cms/asset/b0670319-d70d-43f5-8b8f-3c4d7f7a64e6/temi_a_2135460_f0002_oc.jpg)
Table 2. Vaccination responses in the QIV and ATIV cohorts.
Figure 3. In (A) Fold Induction Rate ((FI mutant virus/FI Wt H1) × 100) of each virus is represented and compared to the Wt, which is 100%, in both cohorts. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (B) Dominance index of HAI titres before and after vaccination with QIV and ATIV vaccines is represented.
![Figure 3. In (A) Fold Induction Rate ((FI mutant virus/FI Wt H1) × 100) of each virus is represented and compared to the Wt, which is 100%, in both cohorts. P-values were determined with the repeated measures one-way Bonferroni’s ANOVA for multiple comparisons test with the Geisser–Greenhouse correction; *P < .05, **P < .01, ***P < .001, ****P < .0001. In (B) Dominance index of HAI titres before and after vaccination with QIV and ATIV vaccines is represented.](/cms/asset/8b57edc3-a0c9-49f9-9465-60ec04a516fd/temi_a_2135460_f0003_oc.jpg)
Supplemental Material
Download MS Word (2 MB)Data availability statement
The data that support the findings of this study are available from the corresponding authors, T.A. and A.G-S. upon reasonable request.