Fig. 3: Antibody responses to the cAd3-Ebola vaccines followed similar dose-dependence and kinetics in the Trial US and Trial UG participants. | npj Vaccines

Fig. 3: Antibody responses to the cAd3-Ebola vaccines followed similar dose-dependence and kinetics in the Trial US and Trial UG participants.

From: Heterologous cAd3-Ebola and MVA-EbolaZ vaccines are safe and immunogenic in US and Uganda phase 1/1b trials

Fig. 3

Baseline-subtracted antibody titers following cAd3-EBOZ or cAd3-EBO vaccination in the US and UG trial participants as assessed by Ebola Zaire GP ELISA. Data expressed as EC90 titers. In (a, b) titers from weeks 4, 24 and 48 post-cAd3 Ebola vaccination are shown as dot plots overlaid with a line at the geometric mean titer (GMT). Titers were compared between groups from the same country and at the same time using Wilcoxon rank-sum test. Statistical significance is noted as follows: α: significant difference from EBOZ Low, β: Significant difference from EBOZ High, γ: Significant difference from EBO Low, λ: Significant difference from all Low, ζ: Significant difference from all EBOZ, π: significant difference from all Low and EBO High, ω: Significant difference from all non-DNA-primed. The n participants for each comparison and the p values are listed in Supplementary Tables 6 and 7. Results from (a, c) are from a previous clinical trial (NCT02231866), and the results have been partially reported28,32. Low n participants in (a) at week 48 are due to recruitment of participants into the subsequent Trial US to receive MVA vaccine (NCT02408913). In (c, d), durability of the vaccine-induced antibody titers are expressed as GMTs. Throughout figure, error bars indicate 95% CIs.

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