Journal: The Lancet Regional Health: Western Pacific
Article Title: Immunogenicity and safety of heterologous immunisation with Ad5-nCOV in healthy adults aged 60 years and older primed with an inactivated SARS-CoV-2 vaccine (CoronaVac): a phase 4, randomised, observer-blind, non-inferiority trial
doi: 10.1016/j.lanwpc.2023.100829
Figure Lengend Snippet: Serum neutralising activities against SARS-CoV2 wild-type and variants of concern (beta, delta and omicron) before and after boosting, measured by ACE2-binding assay. Neutralising capacity measured by ACE2-binding assay in serum of participants who had received heterologous Convidecia and homologous CoronaVac immunisation at day 0 (a) and day 14 (b). Inhibition of ACE2 binding was measured against the wide-type, beta, delta, and omicron Spike proteins. Horizontal bars show the median, and error bars indicate interquartile range (IQR). Group A, primed with two doses of CoronaVac and given one dose of Convidecia (n = 50); Group B, primed with two doses of CoronaVac and given one dose of CoronaVac (n = 50); ACE2, angiotensin-converting enzyme 2.
Article Snippet: Additionally, we used the Spike- ACE2 binding inhibition assay (Meso Scale Discovery (MSD) platform) to test the functional neuralization capacity in samples from the first 100 participants in the three-dose regimen (50 each from the homologous and heterologous boost cohorts) as a post-hoc measurement for cross-reaction of beta (B.1.351), delta (B.1.617.2), and omicron subvariants (BA.2, BA.3, BA.4 and BA.5).
Techniques: Binding Assay, Inhibition