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Neutralizing Immunity Induced Against the Omicron BA.1 and BA.2 Variants in Vaccine Breakthrough Infections
- Brazer, Noah;
- Morris, Mary Kate;
- Servellita, Venice;
- Anglin, Khamal;
- Saldhi, Prachi;
- Garcia-Knight, Miguel;
- Bethancourt, Sutana;
- Sotomayor-Gonzalez, Alicia;
- Wang, Baolin;
- Foresythe, Abiodun;
- Nguyen, Jenny;
- Gliwa, Amelia S;
- Pineda-Ramirez, Jesus;
- Sanchez, Ruth Diaz;
- Zhang, Yueyuan;
- Ott, Melanie;
- Wadford, Debra A;
- Andino, Raul;
- Kelly, J Daniel;
- Hanson, Carl;
- Chiu, Charles Y
- et al.
Published Web Location
https://doi.org/10.1093/infdis/jiac384Abstract
Background
As of early 2022, the Omicron variants are the predominant circulating lineages globally. Understanding neutralizing antibody responses against Omicron BA.1 and BA.2 after vaccine breakthrough infections will provide insights into BA.2 infectivity and susceptibility to subsequent reinfection.Methods
Live virus neutralization assays were used to study immunity against Delta and Omicron BA.1 and BA.2 variants in samples from 86 individuals, 24 unvaccinated (27.9%) and 62 vaccinated (72.1%), who were infected with Delta (n = 42, 48.8%) or BA.1 (n = 44, 51.2%). Among the 62 vaccinated individuals, 39 were unboosted (62.9%), whereas 23 were boosted (37.1%).Results
In unvaccinated infections, neutralizing antibodies (nAbs) against the three variants were weak or undetectable, except against Delta for Delta-infected individuals. Both Delta and BA.1 breakthrough infections resulted in strong nAb responses against ancestral wild-type and Delta lineages, but moderate nAb responses against BA.1 and BA.2, with similar titers between unboosted and boosted individuals. Antibody titers against BA.2 were generally higher than those against BA.1 in breakthrough infections.Conclusions
These results underscore the decreased immunogenicity of BA.1 compared to BA.2, insufficient neutralizing immunity against BA.2 in unvaccinated individuals, and moderate to strong neutralizing immunity induced against BA.2 in Delta and BA.1 breakthrough infections.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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