Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infections

Updated vaccines based on Omicron subvariants have started to being rolled out. Analysis of antibody response in individuals with two or three vaccine doses suggests that BA.2 breakthrough infection barely increases cross-neutralization capacity against BA.4/5 or BA.2.75.

Bibliographic Details
Main Authors: Bin Ju, Qing Fan, Miao Wang, Xuejiao Liao, Huimin Guo, Haiyan Wang, Xiangyang Ge, Lei Liu, Zheng Zhang
Format: Article
Language:English
Published: Nature Portfolio 2022-11-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-022-34400-8
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author Bin Ju
Qing Fan
Miao Wang
Xuejiao Liao
Huimin Guo
Haiyan Wang
Xiangyang Ge
Lei Liu
Zheng Zhang
author_facet Bin Ju
Qing Fan
Miao Wang
Xuejiao Liao
Huimin Guo
Haiyan Wang
Xiangyang Ge
Lei Liu
Zheng Zhang
author_sort Bin Ju
collection DOAJ
description Updated vaccines based on Omicron subvariants have started to being rolled out. Analysis of antibody response in individuals with two or three vaccine doses suggests that BA.2 breakthrough infection barely increases cross-neutralization capacity against BA.4/5 or BA.2.75.
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spelling doaj.art-ac22485f396246829edeef99d34e164b2022-12-22T02:52:01ZengNature PortfolioNature Communications2041-17232022-11-011311610.1038/s41467-022-34400-8Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infectionsBin Ju0Qing Fan1Miao Wang2Xuejiao Liao3Huimin Guo4Haiyan Wang5Xiangyang Ge6Lei Liu7Zheng Zhang8Institute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalInstitute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People’s HospitalUpdated vaccines based on Omicron subvariants have started to being rolled out. Analysis of antibody response in individuals with two or three vaccine doses suggests that BA.2 breakthrough infection barely increases cross-neutralization capacity against BA.4/5 or BA.2.75.https://doi.org/10.1038/s41467-022-34400-8
spellingShingle Bin Ju
Qing Fan
Miao Wang
Xuejiao Liao
Huimin Guo
Haiyan Wang
Xiangyang Ge
Lei Liu
Zheng Zhang
Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infections
Nature Communications
title Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infections
title_full Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infections
title_fullStr Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infections
title_full_unstemmed Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infections
title_short Antigenic sin of wild-type SARS-CoV-2 vaccine shapes poor cross-neutralization of BA.4/5/2.75 subvariants in BA.2 breakthrough infections
title_sort antigenic sin of wild type sars cov 2 vaccine shapes poor cross neutralization of ba 4 5 2 75 subvariants in ba 2 breakthrough infections
url https://doi.org/10.1038/s41467-022-34400-8
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