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Journal: Dose-dependent serological profiling of AdCLD-CoV19-1 vaccine in adults. (Pubmed Central) - Jan 28, 2025 Using a systems serology approach, we demonstrated significant dose-dependent differences in the humoral immune responses induced by the AdCLD-CoV19-1 chimeric adenovirus-based severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine, particularly against the SARS-CoV-2 spike 2 domain. These findings highlight the importance of assessing not only neutralizing antibody titers but also the quality and functionality of antibody responses when evaluating vaccine efficacy.
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Preclinical, Journal: Boosting with variant-matched adenovirus-based vaccines promotes neutralizing antibody responses against SARS-CoV-2 Omicron sublineages in mice. (Pubmed Central) - Mar 4, 2024 Previously, we developed AdCLD-CoV19-1, a non-replicating recombinant adenoviral vector that encodes the receptor binding domain of the spike protein of the ancestral SARS-CoV-2 strain...Of note, boosting with a vaccine targeting the BA.1 or BA.2 Omicron subvariant was most effective in neutralization against the pseudo-virus of BA.2.75 strain, whereas BA.4.1/5-adapted booster shots were most effective in neutralization against BQ.1, BQ1.1, and BF.7. Therefore, it is imperative to develop a vaccination strategy that can cover the unique spike mutations of currently circulating Omicron subvariants to prevent the next wave of COVID-19.
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Journal: Strategy to develop broadly effective multivalent COVID-19 vaccines against emerging variants based on Ad5/35 platform. (Pubmed Central) - Mar 1, 2024 We developed bivalent vaccine AdCLD-CoV19-1 BA.5/BA.2.75 and trivalent vaccines AdCLD-CoV19-1 XBB/BN.1/BQ.1.1 and AdCLD-CoV19-1 XBB.1.5/BN.1/BQ.1.1 using an Ad5/35 platform-based non-replicating recombinant adenoviral vector...We found that the BA.5/BA.2.75 bivalent and the XBB/BN.1/BQ.1.1 and XBB.1.5/BN.1/BQ.1.1 trivalent vaccines exhibited improved cross-neutralization ability compared to their respective monovalent vaccines. These data suggest that the developed multivalent vaccines enhance immunity against circulating Omicron subvariants and effectively elicit neutralizing antibodies across a broad spectrum of SARS-CoV-2 variants.
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Enrollment change, Trial completion date, Trial termination, Trial primary completion date: Safety and Immunogenicity of COVID-19 Vaccine, AdCLD-CoV19-1 (clinicaltrials.gov) - Jun 22, 2023 P2b, N=4, Terminated, Active, not recruiting --> Completed N=200 --> 4 | Trial completion date: May 2024 --> Nov 2022 | Not yet recruiting --> Terminated | Trial primary completion date: May 2024 --> Nov 2022; Study early terminated based on the sponsor(manufacture)'s decision
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