Ad26.COV2.S breakthrough infections induce high titers of neutralizing antibodies against Omicron and other SARS-CoV-2 variants of concern.

Ad26.COV2.S 突破性感染可诱导产生针对 Omicron 和其他令人担忧的 SARS-CoV-2 变种的高滴度中和抗体

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作者:Kitchin Dale, Richardson Simone I, van der Mescht Mieke A, Motlou Thopisang, Mzindle Nonkululeko, Moyo-Gwete Thandeka, Makhado Zanele, Ayres Frances, Manamela Nelia P, Spencer Holly, Lambson Bronwen, Oosthuysen Brent, Kaldine Haajira, du Pisanie Marizane, Mennen Mathilda, Skelem Sango, Williams Noleen, Ntusi Ntobeko A B, Burgers Wendy A, Gray Glenda G, Bekker Linda-Gail, Boswell Michael T, Rossouw Theresa M, Ueckermann Veronica, Moore Penny L
The Janssen (Johnson & Johnson) Ad26.COV2.S non-replicating viral vector vaccine has been widely deployed for COVID-19 vaccination programs in resource-limited settings. Here we confirm that neutralizing and binding antibody responses to Ad26.COV2.S vaccination are stable for 6 months post-vaccination, when tested against multiple SARS-CoV-2 variants. Secondly, using longitudinal samples from individuals who experienced clinically mild breakthrough infections 4 to 5 months after vaccination, we show dramatically boosted binding antibodies, Fc effector function, and neutralization. These high titer responses are of similar magnitude to humoral immune responses measured in convalescent donors who had been hospitalized with severe illness, and are cross-reactive against diverse SARS-CoV-2 variants, including the neutralization-resistant Omicron (B.1.1.529) variant that currently dominates global infections, as well as SARS-CoV-1. These data have implications for population immunity in areas where the Ad26.COV2.S vaccine has been widely deployed, but where ongoing infections continue to occur at high levels.

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