Ad26.COV2.S breakthrough infections induce high titers of neutralizing antibodies against Omicron and other SARS-CoV-2 variants of concern
0301 basic medicine
Ad26.COV2.S
COVID-19 Vaccines
Ad26COVS1
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
COVID-19
Viral Vaccines
Omicron (B.1.1.529) variant
Infections
Antibodies, Viral
Antibodies, Neutralizing
3. Good health
03 medical and health sciences
Report
Humans
Vaccine
DOI:
10.1016/j.xcrm.2022.100535
Publication Date:
2022-02-10T03:50:38Z
AUTHORS (25)
ABSTRACT
AbstractThe 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 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 severely ill, hospitalized donors, and are cross-reactive against diverse SARS-CoV-2 variants, including the extremely 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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