| Literature DB >> 36182684 |
Hye Won Jeong1, Se-Mi Kim2, Min Kyung Jung3, Ji Yun Noh4, Ji-Seung Yoo2, Eun-Ha Kim5, Young-Il Kim2, Kwangmin Yu5, Seung-Gyu Jang6, Juryeon Gil5, Mark Anthony Casel6, Rollon Rare6, Jeong Ho Choi5, Hee-Sung Kim1, Jun Hyoung Kim7, Jihye Um8, Chaeyoon Kim3, Yeonjae Kim9, Bum Sik Chin9, Sungmin Jung10, Jun Yong Choi11, Kyoung-Ho Song12, Yong-Dae Kim13, Jun-Sun Park8, Joon Young Song14, Eui-Cheol Shin15, Young Ki Choi16.
Abstract
Omicron has become the globally dominant severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant, creating additional challenges due to its ability to evade neutralization. Here, we report that neutralizing antibodies against Omicron variants are undetected following COVID-19 infection with ancestral or past SARS-CoV-2 variant viruses or after two-dose mRNA vaccination. Compared with two-dose vaccination, a three-dose vaccination course induces broad neutralizing antibody responses with improved durability against different SARS-CoV-2 variants, although neutralizing antibody titers against Omicron remain low. Intriguingly, among individuals with three-dose vaccination, Omicron breakthrough infection substantially augments serum neutralizing activity against a broad spectrum of SARS-CoV-2 variants, including Omicron variants BA.1, BA.2, and BA.5. Additionally, after Omicron breakthrough infection, memory T cells respond to the spike proteins of both ancestral and Omicron SARS-CoV-2 by producing cytokines with polyfunctionality. These results suggest that Omicron breakthrough infection following three-dose mRNA vaccination induces pan-SARS-CoV-2 immunity that may protect against emerging SARS-CoV-2 variants of concern.Entities:
Keywords: D614G; Omicron BA.1; Omicron BA.2; SARS-CoV-2; T cell immune response; ancestral; breakthrough infection; cross-neutralization; mRNA vaccine; recovered patient; variants of concern
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Year: 2022 PMID: 36182684 PMCID: PMC9482837 DOI: 10.1016/j.xcrm.2022.100764
Source DB: PubMed Journal: Cell Rep Med ISSN: 2666-3791