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Enhanced antibody responses in fully vaccinated individuals against pan-SARS-CoV-2 variants following Omicron breakthrough infection

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Title
Enhanced antibody responses in fully vaccinated individuals against pan-SARS-CoV-2 variants following Omicron breakthrough infection
Author(s)
Jeong, Hye Won; Se-Mi Kim; Min Kyung Jung; Noh, Ji Yun; Ji-Seung Yoo; Kim, Eun-Ha; Young-Il Kim; Yu, Kwangmin; Seung-Gyu Jang; Gil, Juryeon; Mark Anthony Casel; Rollon Rare; Choi, Jeong Ho; Kim, Hee-Sung; Kim, Jun Hyoung; Um, Jihye; Chaeyoon Kim; Kim, Yeonjae; Chin, Bum Sik; Jung, Sungmin; Choi, Jun Yong; Song, Kyoung-Ho; Kim, Yong-Dae; Park, Jun-Sun; Song, Joon Young; Eui-Cheol Shin; Young Ki Choi
Publication Date
2022-10
Journal
Cell Reports Medicine, v.3, no.10
Publisher
Cell Press
Abstract
© 2022 The Author(s)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.
URI
https://pr.ibs.re.kr/handle/8788114/12700
DOI
10.1016/j.xcrm.2022.100764
ISSN
2666-3791
Appears in Collections:
Korea Virus Research Institute(한국바이러스기초연구소) > Center for Study of Emerging and Re-emerging Viruses(신변종 바이러스 연구센터) > 1. Journal Papers (저널논문)
Korea Virus Research Institute(한국바이러스기초연구소) > Center for Viral Immunology(바이러스 면역 연구센터) > 1. Journal Papers (저널논문)
Korea Virus Research Institute(한국바이러스기초연구소) > 1. Journal Papers (저널논문)
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