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Vaccine . Low neutralization of SARS-CoV-2 Omicron BA.5.2.48 and XBB.1 sub-variants in response to breakthrough infection by booster

tetano

Editor, Senior Moderator
Vaccine


. 2024 May 6:S0264-410X(24)00532-2.
doi: 10.1016/j.vaccine.2024.04.093. Online ahead of print. Low neutralization of SARS-CoV-2 Omicron BA.5.2.48 and XBB.1 sub-variants in response to breakthrough infection by booster

Jianhua Li[SUP] 1 [/SUP], Liming Gong[SUP] 1 [/SUP], Jiaxuan Li[SUP] 2 [/SUP], Zhenyu Gong[SUP] 1 [/SUP], Xiaoxiao Wang[SUP] 1 [/SUP], Hao Yan[SUP] 1 [/SUP], Yanjun Zhang[SUP] 3 [/SUP], Haiyan Mao[SUP] 4 [/SUP], Keda Chen[SUP] 5 [/SUP]



Affiliations
Abstract

To assess the levels of and neutralizing antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its mutants in serum samples from patients with breakthrough infection. Sixty-four patients with breakthrough infections were recruited for this cross-sectional study. All samples were used to neutralizing antibodies (nAbs) against SARS-CoV-2 and its mutants using a focused reduction neutralization assay. A total of 512 serum samples were obtained from unvaccinated patients who received one dose of vaccine (n = 12), received two doses of vaccine (n = 15), and received three doses of vaccine (n = 37). The geometric mean titer (GMT) of neutralizing antibodies against the Omicron subvariant was significantly lower (GMT 66.8 and 56.1) compared to the original strain, regardless of whether two or three doses of vaccine were administered. This result highlights that sera from breakthrough infections induce broad neutralization, but Omicron XBB.1.16 exhibits high immune evasion potential.

Keywords: Breakthrough infection; COVID-19; Cross-neutralization; Omicron; Pandemic; SARS-CoV-2; Vaccination.

 
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